Z Gastroenterol 2013; 51(8): 753-854
DOI: 10.1055/s-0033-1350264
Leitlinie
© Georg Thieme Verlag KG Stuttgart · New York

S3-Leitlinie Kolorektales Karzinom Version 1.0 – Juni 2013 AWMF-Registernummer: 021/007OL

S3-Guideline Colorectal Cancer Version 1.0
C. Pox
1   Medizinische Klinik, Knappschaftskrankenhaus GmbH Bochum, Ruhr-Universität Bochum, Bochum
,
S. Aretz
2   Institut für Humangenetik, Universitätsklinik Bonn, Bonn
,
S. C. Bischoff
3   Institut f. Ernährungsmedizin/Prävention Universität Hohenheim, Stuttgart
,
U. Graeven
4   Medizinische Klinik I, Krankenhaus St. Franziskus, Mönchengladbach
,
M. Hass
5   Deutsche ILCO e.V., Bonn
,
P. Heußner
6   Medizinische Klinik und Poliklinik III, Klinikum der Universität München, München
,
W. Hohenberger
7   Chirurgische Klinik, Universitätsklinikum Erlangen, Erlangen
,
A. Holstege
8   Medizinische Klinik I, Klinikum Landshut gGmbH, Landshut
,
J. Hübner
9   Komplementäre Onkologie, Centrum für Tumorerkrankungen J. W. Goethe-Universität, Frankfurt
,
F. Kolligs
10   Medizinische Klinik und Poliklinik II, Klinikum der Universität München, München
,
M. Kreis
11   Chirurgische Klinik I, Charité- Universität Berlin, Campus Benjamin Fränklin, Berlin
,
P. Lux
7   Chirurgische Klinik, Universitätsklinikum Erlangen, Erlangen
,
J. Ockenga
12   Medizinische Klinik II, Klinikum Bremen-Mitte, Bremen
,
R. Porschen
13   Medizinische Klinik, Klinikum Bremen-Ost, Bremen
,
S. Post
14   Chirurgische Klinik, Universitätsklinikum Mannheim GmbH, Mannheim
,
N. Rahner
15   Institut f. Humangenetik u. Anthropologie, Heinrich Heine Universität, Düsseldorf
,
A. Reinacher-Schick
16   Abteilung für Hämatologie/Onkologie, St. Josef Hospital Bochum, Ruhr-Universität Bochum, Bochum
,
J. F. Riemann
17   Stiftung Lebensblicke, Ludwigshafen
,
R. Sauer
18   Strahlenklinik, Universität Erlangen/Nürnberg, Erlangen
,
A. Sieg
19   Gastroenterologische Schwerpunktpraxis, Heidelberg
,
W. Scheppach
20   Gastroenterologische Klinik, Stiftung Juliusspital Würzburg, Würzburg
,
W. Schmitt
21   I. Med. Abteilung, Städtisches Krankenhaus München-Neuperlach, München
,
H. J. Schmoll
22   Klinik und Poliklinik für Innere Medizin IV, Universität Halle, Halle
,
K. Schulmann
23   Klinik für Innere Medizin, Klinikum Arnsberg, St. Johannes-Hospital, MVZ Arnsberg
,
A. Tannapfel
24   Pathologisches Institut der Ruhr Universität Bochum, Bochum
,
W. Schmiegel
1   Medizinische Klinik, Knappschaftskrankenhaus GmbH Bochum, Ruhr-Universität Bochum, Bochum
› Author Affiliations
Further Information

Publication History

Publication Date:
16 August 2013 (online)

1. Informationen zu dieser Leitlinie

1.1. Herausgeber

Leitlinienprogramm Onkologie der AWMF, Deutschen Krebsgesellschaft e. V. und Deutschen Krebshilfe e. V.


#

1.2. Federführende Fachgesellschaft

Deutsche Gesellschaft für Verdauungs- und Stoffwechselkrankheiten (DGVS)

Steuerungsgruppe für Planung und Durchführung über DGVS:
Univ.-Prof. Dr. Wolff Schmiegel
Dr. Christian P. Pox


#

1.3. Finanzierung der Leitlinie

Diese Leitlinie wurde von der Deutschen Krebshilfe im Rahmen des Onkologischen Leitlinienprogramms gefördert.


#

1.4. Kontakt

Leitlinienprogramm Onkologie Office
c/o Deutsche Krebsgesellschaft e. V.
Kuno-Fischer-Str. 8
14 057 Berlin

leitlinienprogramm@krebsgesellschaft.de
www.leitlinienprogramm-onkologie.de


#

1.5. Zitierweise

Leitlinienprogramm Onkologie (Deutsche Krebsgesellschaft, Deutsche Krebshilfe, AWMF): S3-Leitlinie Kolorektales Karzinom, Langversion 1.0, AWMF Registernummer: 021 – 007OL, http://leitlinienprogramm-onkologie.de/Leitlinien.7.0.html


#

1.6. Besonderer Hinweis

Die Medizin unterliegt einem fortwährenden Entwicklungsprozess, sodass alle Angaben, insbesondere zu diagnostischen und therapeutischen Verfahren, immer nur dem Wissensstand zurzeit der Drucklegung der Leitlinie entsprechen können. Hinsichtlich der angegebenen Empfehlungen zur Therapie und der Auswahl sowie Dosierung von Medikamenten wurde die größtmögliche Sorgfalt beachtet. Gleichwohl werden die Benutzer aufgefordert, die Beipackzettel und Fachinformationen der Hersteller zur Kontrolle heranzuziehen und im Zweifelsfall einen Spezialisten zu konsultieren. Fragliche Unstimmigkeiten sollen bitte im allgemeinen Interesse der OL-Redaktion mitgeteilt werden.

Der Benutzer selbst bleibt verantwortlich für jede diagnostische und therapeutische Applikation, Medikation und Dosierung.

In dieser Leitlinie sind eingetragene Warenzeichen (geschützte Warennamen) nicht besonders kenntlich gemacht. Es kann also aus dem Fehlen eines entsprechenden Hinweises nicht geschlossen werden, dass es sich um einen freien Warennamen handelt.

Das Werk ist in allen seinen Teilen urheberrechtlich geschützt. Jede Verwertung außerhalb der Bestimmung des Urhebergesetzes ist ohne schriftliche Zustimmung des Leitlinienprogramms Onkologie (OL) unzulässig und strafbar. Kein Teil des Werkes darf in irgendeiner Form ohne schriftliche Genehmigung des OL reproduziert werden. Dies gilt insbesondere für Vervielfältigungen, Übersetzungen, Mikroverfilmungen und die Einspeicherung, Nutzung und Verwertung in elektronischen Systemen, Intranets und dem Internet.


#

1.7. Ziele des Leitlinienprogramms Onkologie

Die Arbeitsgemeinschaft der Wissenschaftlichen Medizinischen Fachgesellschaften e. V., die Deutsche Krebsgesellschaft e. V. und die Deutsche Krebshilfe e. V. haben sich mit dem Leitlinienprogramm Onkologie (OL) das Ziel gesetzt, gemeinsam die Entwicklung und Fortschreibung und den Einsatz wissenschaftlich begründeter und praktikabler Leitlinien in der Onkologie zu fördern und zu unterstützen. Die Basis dieses Programms beruht auf den medizinisch-wissenschaftlichen Erkenntnissen der Fachgesellschaften und der DKG, dem Konsens der medizinischen Fachexperten, Anwender und Patienten sowie auf dem Regelwerk für die Leitlinienerstellung der AWMF und der fachlichen Unterstützung und Finanzierung durch die Deutsche Krebshilfe. Um den aktuellen Stand des medizinischen Wissens abzubilden und den medizinischen Fortschritt zu berücksichtigen, müssen Leitlinien regelmäßig überprüft und fortgeschrieben werden. Die Anwendung des AWMF-Regelwerks soll hierbei Grundlage zur Entwicklung qualitativ hochwertiger onkologischer Leitlinien sein. Da Leitlinien ein wichtiges Instrument der Qualitätssicherung und des Qualitätsmanagements in der Onkologie darstellen, sollten sie gezielt und nachhaltig in den Versorgungsalltag eingebracht werden. So sind aktive Implementierungsmaßnahmen und auch Evaluationsprogramme ein wichtiger Bestandteil der Förderung des Leitlinienprogramms Onkologie. Ziel des Programms ist es, in Deutschland professionelle und mittelfristig finanziell gesicherte Voraussetzungen für die Entwicklung und Bereitstellung hochwertiger Leitlinien zu schaffen. Denn diese hochwertigen Leitlinien dienen nicht nur dem strukturierten Wissenstransfer, sondern können auch in der Gestaltung der Strukturen des Gesundheitssystems ihren Platz finden. Zu erwähnen sind hier evidenzbasierte Leitlinien als Grundlage zum Erstellen und Aktualisieren von Disease Management Programmen oder die Verwendung von aus Leitlinien extrahierten Qualitätsindikatoren im Rahmen der Zertifizierung von Organtumorzentren.


#

1.8. Autoren dieser Leitlinie

C. Pox, S. Aretz, S. C. Bischoff, U. Graeven, M. Hass, P. Heußner, W. Hohenberger, A. Holstege, J. Hübner, F. Kolligs, M. Kreis, P. Lux, J. Ockenga, R. Porschen, S. Post, N. Rahner, A. Reinacher-Schick, J. F. Riemann, R. Sauer, A. Sieg, W. Scheppach, W. Schmitt, H.-J. Schmoll, K. Schulmann, A. Tannapfel, W. Schmiegel

1.8.1. Zusammensetzung der Leitliniengruppe 2011/2012

Die Fachexpertengruppe für die Aktualisierung der Kapitel 3, 4, 5, 7, 10 (s. Abschnitt 2.2.1) setzte sich aus insgesamt 53 Mandatsträgern und Plenumsmitgliedern folgender Fachgesellschaften, Berufsverbände und Patientenvereinigungen zusammen:

  • Fachgesellschaften

    • DKG (Deutsche Krebsgesellschaft)

      • ASORS (AG der DKG „Supportive Maßnahmen in der Onkologie, Rehabilitation und Sozialmedizin“)

      • PRIO (AG der DKG Prävention und integrative Medizin in der Onkologie)

      • PSO (AG der DKG: Dt. Arbeitsgemeinschaft für Psychoonkologie)

    • KOK (AG der DKG: Konferenz Onkologische Kranken- und Kinderkrankenpflege)

    • DGVS (Deutsche Gesellschaft für Verdauungs- und Stoffwechselkrankheiten)

    • DEGAM (Deutsche Gesellschaft für Allgemeinmedizin und Familienmedizin)

    • DEGRO (Deutsche Gesellschaft für Radioonkologie)

    • DGAV (Deutsche Gesellschaft für Allgemein- und Viszeralchirurgie)

      • CACP (Chirurgische Arbeitsgemeinschaft für Colo-Proktologie)

      • CAMIC (Chirurgische Arbeitsgemeinschaft für Minimal-invasive Chirurgie)

      • CAO-V (Chirurgische Arbeitsgemeinschaft für Onkologie)

    • DGCH (Deutsche Gesellschaft für Chirurgie)

    • DGEM (Deutsche Gesellschaft für Ernährungsmedizin)

    • DGHO (Deutsche Gesellschaft für Hämatologie und Onkologie)

    • DGIM (Deutsche Gesellschaft für Innere Medizin)

    • DGKL (Deutsche Gesellschaft für Klinische Chemie und Laboratoriumsmedizin)

    • DGN (Deutsche Gesellschaft für Nuklearmedizin)

    • DGP (Deutsche Gesellschaft für Pathologie)

    • DRG (Deutsche Röntgengesellschaft)

    • GfH (Deutsche Gesellschaft für Humangenetik)

  • andere Institutionen

    • bng (Berufsverband Niedergelassener Gastroenterologen Deutschlands e. V.)

    • HÄV (Deutscher Hausärzteverband)

    • AQUA (Institut für angewandte Qualitätsförderung und Forschung im Gesundheitswesen)

    • ZI (Zentralinstitut der Kassenärztlichen Versorgung in der BRD)

    • Felix-Burda-Stiftung

    • Stiftung Lebensblicke

  • Patientenvereinigungen

    • DCCV (Deutsche Morbus Crohn/Colitis Ulcerosa Vereinigung)

    • Deutsche ILCO (Vereinigung für Stomaträger und für Menschen mit Darmkrebs)

[Tab. 1] zeigt die Zusammensetzung der Leitliniengruppe 2011/2012 unter der Leitung von Prof. Dr. W. Schmiegel (DKG, DGVS)

Tab. 1

Zusammensetzung der Arbeitsgruppen für die Aktualisierung der Kapitel 3, 4, 5, 7, 10.

Kapitel 3: Prävention asymptomatische Bevölkerung

Koordinator: J. F. Riemann

DGIM, DGVS, Stiftung Lebensblicke

Mitglieder:

S. C. Bischoff


DGEM, DGVS

F. Kolligs

DGVS

J. Ockenga

DGEM, DGVS

W. Scheppach

DGEM, DGVS

Kapitel 4: Früherkennung/Vorsorge asymptomatische Bevölkerung

Koordinatoren: C. Pox, A. Sieg

beide DGVS

Mitglieder:

L. Altenhofen


ZI

H-J. Brambs

DRG, DGAM

H. Brenner

Experte (nicht stimmberechtigt)

P. Engeser

HÄV

A. Theilmeier

bng, DGVS

Kapitel 5: Risikogruppen

Koordinatoren:

N. Rahner

K. Schulmann


GfH

DGVS

G. Baretton

DGP

B. Bokemeyer

bng, DGVS

J. Epplen

DGHG

U. Melle

DGVS

R. Porschen

DGVS

J. Weitz

DGAV

C. Witte

DCCV

Kapitel 7: Präoperative Diagnostik und Chirurgie

Koordinatoren:

W. Hohenberger

S. Post


DKG, DGAV

DKG, DGAV, CACP

M. Anthuber

DGAV

W. Bechstein

DGAV

U. Graeven

DGVS

M. Haß

Dt. ILCO

M. Heike

DGHO

K.-W. Jauch

DGAV

T. Kirchner

DGP

H. Lang

DKG, DGAV, CAO-V

K-H. Link

DKG, DGAV

P. Pereira

DRG

H-R. Raab

DGAV

A. Reinacher-Schick

DGVS

C. Rödel

DEGRO

M. Sailer

DGAV

R. Sauer

DEGRO

K. Scheidhauer

DGN

A. Tannapfel

DGP

T. Vogl

DRG

C. Wagener

DGKL

M. Walz

DGAV, CAMIC

C. Wittekind

DGP

Kapitel 10: Nachsorge

Koordinator: A. Holstege

DGVS

Mitglieder:

P. Heußner


PSO

T. Höhler

DGHO

J. Hübner

DKG, PRIO

J. Körber

DKG, ASORS

M. Landenberger

DKG, KOK

H. Link

DKG, ASORS

Zusätzlich beim Plenum beteiligt

S. Ludt

AQUA

P. Lux

Mit-Autor (nicht stimmberechtigt)

C. Maar

Felix-Burda-Stiftung


#

1.8.2. Koordinatoren der Leitliniengruppe 2007/2008

Die Koordinatoren bei der Überarbeitung der Kapitel 6, 8 und 9 in 2007/2008 waren:

Kapitel 6 – Endoskopie: Durchführung und Polypenmanagement:
J. F. Riemann, W. Schmitt

Kapitel 8 – Adjuvante und neoadjuvante Therapie:
R. Porschen, R. Sauer

Kapitel 9 – Therapeutisches Vorgehen bei Metastasierung und in der palliativen Situation: U. Graeven, H-J. Schmoll


#

1.8.3. Zusammensetzung der AG Qualitätsindikatoren

Die Entwicklung der Vorschläge zu Qualitätsindikatoren erfolgte durch die in [Tab. 2] aufgeführte Arbeitsgruppe.

Tab. 2

Zusammensetzung der AG Qualitätsindikatoren.

Name

Institution

Koordinatoren:

W. Schmiegel

C. Pox


DKG, DGVS

DGVS

Mitglieder:

M. Haß


Dt. ILCO

W. Hohenberger

DKG, DGAV

A. Holstege

DGVS

F. Kolligs

DGVS

M. Klinkhammer-Schalke

Arbeitsgemeinschaft Deutscher Tumorzentren (ADT)

I. Kopp

AWMF, Leitlinienprogramm Onkologie

S. Ludt

AQUA

J. Ockenga

DGVS

S. Post

DKG, DGAV, CACP

A. Tannapfel

DGP

S. Wesselmann

Deutsche Krebsgesellschaft (DKG), Bereich Zertifizierung


#

1.8.4. Methodische Begleitung

Durch das Leitlinienprogramm Onkologie:

  • Prof. Dr. Ina Kopp (AWMF), Marburg

  • Dr. Markus Follmann, MPH MSc (DKG), Berlin


#
#

1.9. Verfügbare Dokumente zur Leitlinie und Implementierung

Bei diesem Dokument handelt es sich um die Langversion der S3-Leitlinie Kolorektales Karzinom, welche über die folgenden Seiten zugänglich ist:

Darüber hinaus wird die Langversion dieser Leitlinie wird in der Zeitschrift für Gastroenterologie veröffentlicht werden.

Neben der Langfassung wird es die folgenden ergänzenden Dokumente zu dieser Leitlinie geben:

  • Kurzversion

  • Leitlinienreport

  • Übersetzung (englisch)

  • Patientenleitlinie

  • Externer Evidenzbericht

Alle diese Dokumente werden ebenfalls auf den oben genannten Homepages abrufbar sein.

Der externe Evidenzbericht wurde zum Kapitel 4 (Vorsorge/Früherkennung) und Teilen des Kapitels 7 (präoperative Diagnostik und Chirurgie) von einer Kooperation der Universität Witten/Herdecke (Institut für Forschung in der Operativen Medizin) mit der Universität Duisburg/Essen (Alfried Krupp von Bohlen und Halbach Stiftungslehrstuhl für Medizinmanagement) erstellt.

Die Erstellung der Patientenleitlinie und die Übersetzung der Langversion ins Englische werden mit Fertigstellung der Leitlinie in Auftrag gegeben.

Eine flächendeckende Verbreitung dieser evidenzbasierten, aktuellen Verhaltensempfehlungen ist insbesondere für die Steigerung der Qualität bei Patienteninformation und -versorgung notwendig. Mithilfe standardisierter Methoden wurden von den Empfehlungen Qualitätsindikatoren abgeleitet. Diese dienen neben der Implementierung in erster Linie der Qualitätssicherung und -steigerung der patientenrelevanten Prozesse.


#
 
  • Literatur

  • 1 Kirkegaard H et al. Association of adherence to lifestyle recommendations and risk of colorectal cancer: a prospective Danish cohort study. BMJ 2010; 341: c5504
  • 2 Halle M, Schoenberg MH. Physical activity in the prevention and treatment of colorectal carcinoma. Dtsch Arztebl Int 2009; 106 (44) 722-727
  • 3 Wolin KY et al. Physical activity and colon cancer prevention: a meta-analysis. Br J Cancer 2009; 100 (04) 611-616
  • 4 Wolin KY, Yan Y, Colditz GA. Physical activity and risk of colon adenoma: a meta-analysis. Br J Cancer 2011; 104 (05) 882-885
  • 5 Wolin KY et al. Leisure-time physical activity patterns and risk of colon cancer in women. Int J Cancer 2007; 121 (12) 2776-2781
  • 6 Friedenreich C et al. Physical activity and risk of colon and rectal cancers: the European prospective investigation into cancer and nutrition. Cancer Epidemiol Biomarkers Prev 2006; 15 (12) 2398-2407
  • 7 Lubin F et al. Nutritional and lifestyle habits and water-fiber interaction in colorectal adenoma etiology. Cancer Epidemiol Biomarkers Prev 1997; 6 (02) 79-85
  • 8 Giacosa A et al. Energy intake, overweight, physical exercise and colorectal cancer risk. Eur J Cancer Prev 1999; 8 (Suppl. 01) S53-S60
  • 9 Friedenreich CM, Orenstein MR. Physical activity and cancer prevention: etiologic evidence and biological mechanisms. J Nutr 2002; 132 (Suppl. 11) 3456S-3464S
  • 10 Terry MB et al. Risk factors for advanced colorectal adenomas: a pooled analysis. Cancer Epidemiol Biomarkers Prev 2002; 11 (07) 622-629
  • 11 Lee IM. Physical activity and cancer prevention – data from epidemiologic studies. Med Sci Sports Exerc 2003; 35 (11) 1823-1827
  • 12 Wei EK et al. Comparison of risk factors for colon and rectal cancer. Int J Cancer 2004; 108 (03) 433-442
  • 13 Martinez ME et al. Physical activity, body mass index, and prostaglandin E2 levels in rectal mucosa. J Natl Cancer Inst 1999; 91 (11) 950-953
  • 14 Giovannucci E. Modifiable risk factors for colon cancer. Gastroenterol Clin North Am 2002; 31 (04) 925-943
  • 15 Giovannucci E. Diet, body weight, and colorectal cancer: a summary of the epidemiologic evidence. J Womens Health (Larchmt) 2003; 12 (02) 173-182
  • 16 Renehan AG et al. Body-mass index and incidence of cancer: a systematic review and meta-analysis of prospective observational studies. Lancet 2008; 371 (9612) 569-578
  • 17 Pischon T et al. Body size and risk of colon and rectal cancer in the European Prospective Investigation Into Cancer and Nutrition (EPIC). J Natl Cancer Inst 2006; 98 (13) 920-931
  • 18 Ning Y, Wang L, Giovannucci EL. A quantitative analysis of body mass index and colorectal cancer: findings from 56 observational studies. Obes Rev 2010; 11 (01) 19-30
  • 19 Terry MB, Neugut AI. Cigarette smoking and the colorectal adenoma-carcinoma sequence: a hypothesis to explain the paradox. Am J Epidemiol 1998; 147 (10) 903-910
  • 20 Almendingen K et al. Smoking and colorectal adenomas: a case-control study. Eur J Cancer Prev 2000; 9 (03) 193-203
  • 21 Chao A et al. Cigarette smoking and colorectal cancer mortality in the cancer prevention study II. J Natl Cancer Inst 2000; 92 (23) 1888-1896
  • 22 Giovannucci E. An updated review of the epidemiological evidence that cigarette smoking increases risk of colorectal cancer. Cancer Epidemiol Biomarkers Prev 2001; 10 (07) 725-731
  • 23 Reid ME et al. Smoking exposure as a risk factor for prevalent and recurrent colorectal adenomas. Cancer Epidemiol Biomarkers Prev 2003; 12 (10) 1006-1011
  • 24 Botteri E et al. Cigarette smoking and adenomatous polyps: a meta-analysis. Gastroenterology 2008; 134 (02) 388-395
  • 25 Botteri E et al. Smoking and colorectal cancer: a meta-analysis. JAMA 2008; 300 (23) 2765-2778
  • 26 Miller PE et al. Dietary patterns and colorectal adenoma and cancer risk: a review of the epidemiological evidence. Nutr Cancer 2010; 62 (04) 413-424
  • 27 Cottet V et al. Dietary patterns and the risk of colorectal adenoma recurrence in a European intervention trial. Eur J Cancer Prev 2005; 14 (01) 21-29
  • 28 Mai V et al. Diet quality and subsequent cancer incidence and mortality in a prospective cohort of women. Int J Epidemiol 2005; 34 (01) 54-60
  • 29 Sansbury LB et al. The effect of strict adherence to a high-fiber, high-fruit and -vegetable, and low-fat eating pattern on adenoma recurrence. Am J Epidemiol 2009; 170 (05) 576-584
  • 30 Wakai K et al. Dietary risk factors for colon and rectal cancers: a comparative case-control study. J Epidemiol 2006; 16 (03) 125-135
  • 31 Beresford SA et al. Low-fat dietary pattern and risk of colorectal cancer: the Women's Health Initiative Randomized Controlled Dietary Modification Trial. JAMA 2006; 295 (06) 643-654
  • 32 Lanza E et al. The polyp prevention trial continued follow-up study: no effect of a low-fat, high-fiber, high-fruit, and -vegetable diet on adenoma recurrence eight years after randomization. Cancer Epidemiol Biomarkers Prev 2007; 16 (09) 1745-1752
  • 33 Dahm CC et al. Dietary fiber and colorectal cancer risk: a nested case-control study using food diaries. J Natl Cancer Inst 2010; 102 (09) 614-626
  • 34 Ishikawa H et al. Randomized trial of dietary fiber and Lactobacillus casei administration for prevention of colorectal tumors. Int J Cancer 2005; 116 (05) 762-767
  • 35 Jacobs ET et al. Fiber, sex, and colorectal adenoma: results of a pooled analysis. Am J Clin Nutr 2006; 83 (02) 343-349
  • 36 Park Y et al. Dietary fiber intake and risk of colorectal cancer: a pooled analysis of prospective cohort studies. JAMA 2005; 294 (22) 2849-2857
  • 37 Robertson DJ et al. Fat, fiber, meat and the risk of colorectal adenomas. Am J Gastroenterol 2005; 100 (12) 2789-2795
  • 38 Austin GL et al. Moderate alcohol consumption protects against colorectal adenomas in smokers. Dig Dis Sci 2008; 53 (01) 116-122
  • 39 Cho E et al. Alcohol intake and colorectal cancer: a pooled analysis of 8 cohort studies. Ann Intern Med 2004; 140 (08) 603-613
  • 40 Mizoue T et al. Alcohol drinking and colorectal cancer in Japanese: a pooled analysis of results from five cohort studies. Am J Epidemiol 2008; 167 (12) 1397-1406
  • 41 Moskal A et al. Alcohol intake and colorectal cancer risk: a dose-response meta-analysis of published cohort studies. Int J Cancer 2007; 120 (03) 664-671
  • 42 Chao A et al. Meat consumption and risk of colorectal cancer. JAMA 2005; 293 (02) 172-182
  • 43 Larsson SC, Wolk A. Meat consumption and risk of colorectal cancer: a meta-analysis of prospective studies. Int J Cancer 2006; 119 (11) 2657-2664
  • 44 Mathew A et al. Meat intake and the recurrence of colorectal adenomas. Eur J Cancer Prev 2004; 13 (03) 159-164
  • 45 Norat T et al. Meat, fish, and colorectal cancer risk: the European Prospective Investigation into cancer and nutrition. J Natl Cancer Inst 2005; 97 (12) 906-916
  • 46 Sinha R et al. Meat, meat cooking methods and preservation, and risk for colorectal adenoma. Cancer Res 2005; 65 (17) 8034-8041
  • 47 Geelen A et al. Fish consumption, n-3 fatty acids, and colorectal cancer: a meta-analysis of prospective cohort studies. Am J Epidemiol 2007; 166 (10) 1116-1125
  • 48 Sugawara Y et al. Fish consumption and the risk of colorectal cancer: the Ohsaki Cohort Study. Br J Cancer 2009; 101 (05) 849-854
  • 49 Pot GK et al. Fish consumption and markers of colorectal cancer risk: a multicenter randomized controlled trial. Am J Clin Nutr 2009; 90 (02) 354-361
  • 50 Je Y, Liu W, Giovannucci E. Coffee consumption and risk of colorectal cancer: a systematic review and meta-analysis of prospective cohort studies. Int J Cancer 2009; 124 (07) 1662-1668
  • 51 Sun CL et al. Green tea, black tea and colorectal cancer risk: a meta-analysis of epidemiologic studies. Carcinogenesis 2006; 27 (07) 1301-1309
  • 52 Zhang X et al. Risk of colon cancer and coffee, tea, and sugar-sweetened soft drink intake: pooled analysis of prospective cohort studies. J Natl Cancer Inst 2010; 102 (11) 771-783
  • 53 Foschi R et al. Citrus fruit and cancer risk in a network of case-control studies. Cancer Causes Control 2010; 21 (02) 237-242
  • 54 Millen AE et al. Fruit and vegetable intake and prevalence of colorectal adenoma in a cancer screening trial. Am J Clin Nutr 2007; 86 (06) 1754-1764
  • 55 Koushik A et al. Fruits, vegetables, and colon cancer risk in a pooled analysis of 14 cohort studies. J Natl Cancer Inst 2007; 99 (19) 1471-1483
  • 56 Limburg PJ et al. Prospective evaluation of trans-fatty acid intake and colorectal cancer risk in the Iowa Women's Health Study. Int J Cancer 2008; 123 (11) 2717-2719
  • 57 Alexander DD et al. Meta-analysis of animal fat or animal protein intake and colorectal cancer. Am J Clin Nutr 2009; 89 (05) 1402-1409
  • 58 Galeone C et al. Fried foods, olive oil and colorectal cancer. Ann Oncol 2007; 18 (01) 36-39
  • 59 Nakamura T et al. Excessive fat restriction might promote the recurrence of colorectal tumors. Nutr Cancer 2010; 62 (02) 154-163
  • 60 Larsson SC et al. Dietary acrylamide intake and risk of colorectal cancer in a prospective cohort of men. Eur J Cancer 2009; 45 (04) 513-516
  • 61 Hogervorst JG et al. Dietary acrylamide intake is not associated with gastrointestinal cancer risk. J Nutr 2008; 138 (11) 2229-2236
  • 62 Mucci LA, Wilson KM. Acrylamide intake through diet and human cancer risk. J Agric Food Chem 2008; 56 (15) 6013-6019
  • 63 Mucci LA, Adami HO, Wolk A. Prospective study of dietary acrylamide and risk of colorectal cancer among women. Int J Cancer 2006; 118 (01) 169-173
  • 64 Bjelakovic G et al. Mortality in randomized trials of antioxidant supplements for primary and secondary prevention: systematic review and meta-analysis. JAMA 2007; 297 (08) 842-857
  • 65 Weingarten MA, Zalmanovici A, Yaphe J. Dietary calcium supplementation for preventing colorectal cancer and adenomatous polyps. Cochrane Database Syst Rev 2008; 1: CD003548
  • 66 Wactawski-Wende J et al. Calcium plus vitamin D supplementation and the risk of colorectal cancer. N Engl J Med 2006; 354 (07) 684-696
  • 67 Sanjoaquin MA et al. Folate intake and colorectal cancer risk: a meta-analytical approach. Int J Cancer 2005; 113 (05) 825-828
  • 68 Wu K et al. A randomized trial on folic acid supplementation and risk of recurrent colorectal adenoma. Am J Clin Nutr 2009; 90 (06) 1623-1631
  • 69 Jaszewski R et al. Folic acid supplementation inhibits recurrence of colorectal adenomas: a randomized chemoprevention trial. World J Gastroenterol 2008; 14 (28) 4492-4498
  • 70 Cole BF et al. Folic acid for the prevention of colorectal adenomas: a randomized clinical trial. JAMA 2007; 297 (21) 2351-2359
  • 71 Logan RF et al. Aspirin and folic acid for the prevention of recurrent colorectal adenomas. Gastroenterology 2008; 134 (01) 29-38
  • 72 Grau MV et al. Prolonged effect of calcium supplementation on risk of colorectal adenomas in a randomized trial. J Natl Cancer Inst 2007; 99 (02) 129-136
  • 73 Wallace K et al. Effect of calcium supplementation on the risk of large bowel polyps. J Natl Cancer Inst 2004; 96 (12) 921-5
  • 74 Hartman TJ et al. The association of calcium and vitamin D with risk of colorectal adenomas. J Nutr 2005; 135 (02) 252-259
  • 75 Lin J et al. Total magnesium intake and colorectal cancer incidence in women. Cancer Epidemiol Biomarkers Prev 2006; 15 (10) 2006-2009
  • 76 Jacobs ET et al. Selenium and colorectal adenoma: results of a pooled analysis. J Natl Cancer Inst 2004; 96 (22) 1669-1675
  • 77 Peters U et al. High serum selenium and reduced risk of advanced colorectal adenoma in a colorectal cancer early detection program. Cancer Epidemiol Biomarkers Prev 2006; 15 (02) 315-320
  • 78 Vinogradova Y et al. Risk of colorectal cancer in patients prescribed statins, nonsteroidal anti-inflammatory drugs, and cyclooxygenase-2 inhibitors: nested case-control study. Gastroenterology 2007; 133 (02) 393-402
  • 79 Bertagnolli MM et al. Celecoxib for the prevention of sporadic colorectal adenomas. N Engl J Med 2006; 355 (09) 873-884
  • 80 Arber N et al. Celecoxib for the prevention of colorectal adenomatous polyps. N Engl J Med 2006; 355 (09) 885-895
  • 81 Baron JA et al. A randomized trial of rofecoxib for the chemoprevention of colorectal adenomas. Gastroenterology 2006; 131 (06) 1674-1682
  • 82 Bardou M, Barkun A, Martel M. Effect of statin therapy on colorectal cancer. Gut 2010; 59 (11) 1572-1585
  • 83 Routine aspirin or nonsteroidal anti-inflammatory drugs for the primary prevention of colorectal cancer: U. S. Preventive Services Task Force recommendation statement. Ann Intern Med 2007; 146 (05) 361-364
  • 84 Flossmann E, Rothwell PM. Effect of aspirin on long-term risk of colorectal cancer: consistent evidence from randomised and observational studies. Lancet 2007; 369 (9573) 1603-1613
  • 85 Rothwell PM et al. Effect of daily aspirin on long-term risk of death due to cancer: analysis of individual patient data from randomised trials. Lancet 2011; 377 (9759) 31-41
  • 86 Chan AT et al. Long-term use of aspirin and nonsteroidal anti-inflammatory drugs and risk of colorectal cancer. JAMA 2005; 294 (08) 914-923
  • 87 Hormone therapy for the prevention of chronic conditions in postmenopausal women: recommendations from the U. S. Preventive Services Task Force. Ann Intern Med 2005; 142 (10) 855-860
  • 88 Farquhar C et al. Long term hormone therapy for perimenopausal and postmenopausal women. Cochrane Database Syst Rev 2009; 2: CD004143
  • 89 Alberts DS et al. Phase III trial of ursodeoxycholic acid to prevent colorectal adenoma recurrence. J Natl Cancer Inst 2005; 97 (11) 846-853
  • 90 DGGG. Hormontherapie (HT) in der Peri- und Postmenopause. 2009
  • 91 Birkner BR. Evidence-based prevention of colorectal carcinoma. Dtsch Med Wochenschr 2003; 128 (49) 2598-2603
  • 92 Winawer SJ et al. Colorectal cancer screening: clinical guidelines and rationale. Gastroenterology 1997; 112 (02) 594-642
  • 93 Imperiale TF et al. Results of screening colonoscopy among persons 40 to 49 years of age. N Engl J Med 2002; 346 (23) 1781-1785
  • 94 Whitlock EP et al. Screening for colorectal cancer: a targeted, updated systematic review for the U. S. Preventive Services Task Force. Ann Intern Med 2008; 149 (09) 638-658
  • 95 Stevens T, Burke CA. Colonoscopy screening in the elderly: when to stop?. Am J Gastroenterol 2003; 98 (08) 1881-1885
  • 96 Kirchgatterer A et al. Colonoscopy and sigmoidoscopy in patients aged eighty years or older. Z Gastroenterol 2002; 40 (12) 951-956
  • 97 Pox CP et al. Efficacy of a Nationwide Screening Colonoscopy Program for Colorectal Cancer. Gastroenterology 2012; 142: 1460-1467
  • 98 Zhang B, Fattah A, Nakama H. Characteristics and survival rate of elderly patients with colorectal cancer detected by immunochemical occult blood screening. Hepatogastroenterology 2000; 47 (32) 414-418
  • 99 Winawer SJ et al. Prevention of colorectal cancer by colonoscopic polypectomy. The National Polyp Study Workgroup. N Engl J Med 1993; 329 (27) 1977-1981
  • 100 Citarda F et al. Efficacy in standard clinical practice of colonoscopic polypectomy in reducing colorectal cancer incidence. Gut 2001; 48 (06) 812-815
  • 101 Zauber AG et al. Colonoscopic polypectomy and long-term prevention of colorectal-cancer deaths. N Engl J Med 2012; 366 (08) 687-696
  • 102 Hol L et al. Screening for colorectal cancer: randomised trial comparing guaiac-based and immunochemical faecal occult blood testing and flexible sigmoidoscopy. Gut 2010; 59 (01) 62-68
  • 103 Quintero E et al. Colonoscopy versus fecal immunochemical testing in colorectal-cancer screening. N Engl J Med 2012; 366 (08) 697-706
  • 104 Bekanntmachungen: Richtlinien des Bundesausschusses der Ärzte und Krankenkassen über die Früherkennung von Krebserkrankungen („Krebsfrüherkennungs-Richtlinien“). Dtsch Arztebl Int 2002; 1 (11) 518
  • 105 Huppe D et al. Effectiveness of screening colonoscopy in a community-based study. Z Gastroenterol 2008; 46 (02) 193-200
  • 106 Kahi CJ et al. Effect of screening colonoscopy on colorectal cancer incidence and mortality. Clin Gastroenterol Hepatol 2009; 7 (07) 770-775 quiz 711
  • 107 Imperiale TF et al. Risk of advanced proximal neoplasms in asymptomatic adults according to the distal colorectal findings. N Engl J Med 2000; 343 (03) 169-174
  • 108 Lieberman DA et al. Use of colonoscopy to screen asymptomatic adults for colorectal cancer. Veterans Affairs Cooperative Study Group 380. N Engl J Med 2000; 343 (03) 162-168
  • 109 Atkin W et al. Single flexible sigmoidoscopy screening to prevent colorectal cancer: baseline findings of a UK multicentre randomised trial. Lancet 2002; 359 (9314) 1291-1300
  • 110 Muller AD, Sonnenberg A. Protection by endoscopy against death from colorectal cancer. A case-control study among veterans. Arch Intern Med 1995; 155 (16) 1741-1748
  • 111 Newcomb PA et al. Screening sigmoidoscopy and colorectal cancer mortality. J Natl Cancer Inst 1992; 84 (20) 1572-1575
  • 112 Selby JV et al. A case-control study of screening sigmoidoscopy and mortality from colorectal cancer. N Engl J Med 1992; 326 (10) 653-657
  • 113 Singh H et al. Predictors of colorectal cancer after negative colonoscopy: a population-based study. Am J Gastroenterol 2010; 105 (03) 663-673 ; quiz 674
  • 114 Brenner H et al. Protection from right- and left-sided colorectal neoplasms after colonoscopy: population-based study. J Natl Cancer Inst 2010; 102 (02) 89-95
  • 115 Brenner H et al. Protection from colorectal cancer after colonoscopy: a population-based, case-control study. Ann Intern Med 2011; 154 (01) 22-30
  • 116 Sieg A, Hachmoeller-Eisenbach U, Eisenbach T. Prospective evaluation of complications in outpatient GI endoscopy: a survey among German gastroenterologists. Gastrointest Endosc 2001; 53: 620-627
  • 117 Rex DK et al. Colonoscopic miss rates of adenomas determined by back-to-back colonoscopies. Gastroenterology 1997; 112 (01) 24-28
  • 118 Rex DK et al. 5-year incidence of adenomas after negative colonoscopy in asymptomatic average-risk persons [see comment]. Gastroenterology 1996; 111 (05) 1178-1181
  • 119 Brenner H et al. Long-term risk of colorectal cancer after negative colonoscopy. J Clin Oncol 2011; 29 (28) 3761-3767
  • 120 Bundesärztekammer: Richtlinien zur prädiktiven genetischen Diagnostik. Dt Ärztebl 2003; 100 (19) A1297-1305
  • 121 Atkin WS et al. Once-only flexible sigmoidoscopy screening in prevention of colorectal cancer: a multicentre randomised controlled trial. Lancet 2010; 375 (9726) 1624-1633
  • 122 Muller AD, Sonnenberg A. Prevention of colorectal cancer by flexible endoscopy and polypectomy. A case-control study of 32,702 veterans. Ann Intern Med 1995; 123 (12) 904-910
  • 123 Newcomb PA et al. Long-term efficacy of sigmoidoscopy in the reduction of colorectal cancer incidence. J Natl Cancer Inst 2003; 95 (08) 622-625
  • 124 Schoen RE et al. Results of repeat sigmoidoscopy 3 years after a negative examination. Jama 2003; 290 (01) 41-48
  • 125 Burke CA, Elder K, Lopez R. Screening for colorectal cancer with flexible sigmoidoscopy: is a 5-yr interval appropriate? A comparison of the detection of neoplasia 3 yr versus 5 yr after a normal examination. Am J Gastroenterol 2006; 101 (06) 1329-1332
  • 126 Winawer SJ et al. Screening for colorectal cancer with fecal occult blood testing and sigmoidoscopy. J Natl Cancer Inst 1993; 85 (16) 1311-1318
  • 127 Lieberman DA, Weiss DG. One-time screening for colorectal cancer with combined fecal occult-blood testing and examination of the distal colon. N Engl J Med 2001; 345 (08) 555-560
  • 128 Gondal G et al. The Norwegian Colorectal Cancer Prevention (NORCCAP) screening study: baseline findings and implementations for clinical work-up in age groups 50-64 years. Scand J Gastroenterol 2003; 38 (06) 635-642
  • 129 Kato J et al. Combination of sigmoidoscopy and a fecal immunochemical test to detect proximal colon neoplasia. Clin Gastroenterol Hepatol 2009; 7 (12) 1341-1346
  • 130 Eliakim R et al. Evaluation of the PillCam Colon capsule in the detection of colonic pathology: results of the first multicenter, prospective, comparative study. Endoscopy 2006; 38 (10) 963-70
  • 131 Schoofs N, Deviere J, Van Gossum A. PillCam colon capsule endoscopy compared with colonoscopy for colorectal tumor diagnosis: a prospective pilot study. Endoscopy 2006; 38 (10) 971-977
  • 132 Van Gossum A et al. Capsule endoscopy versus colonoscopy for the detection of polyps and cancer. N Engl J Med 2009; 361 (03) 264-270
  • 133 Spada C et al. Meta-analysis shows colon capsule endoscopy is effective in detecting colorectal polyps. Clin Gastroenterol Hepatol 2010; 8 (06) 516-522
  • 134 Gay G et al. Could the colonic capsule PillCam Colon be clinically useful for selecting patients who deserve a complete colonoscopy? Results of clinical comparison with colonoscopy in the perspective of colorectal cancer screening. Am J Gastroenterol 2010; 105 (05) 1076-1086
  • 135 Eliakim R et al. Prospective multicenter performance evaluation of the second-generation colon capsule compared with colonoscopy. Endoscopy 2009; 41 (12) 1026-1031
  • 136 Spada C et al. Second-generation colon capsule endoscopy compared with colonoscopy. Gastrointest Endosc 2011; 74 (03) 581-589 e1
  • 137 Mandel JS et al. Reducing mortality from colorectal cancer by screening for fecal occult blood. Minnesota Colon Cancer Control Study. N Engl J Med 1993; 328 (19) 1365-1371
  • 138 Zhu MM et al. Comparison of immunochemical and guaiac-based fecal occult blood test in screening and surveillance for advanced colorectal neoplasms: a meta-analysis. J Dig Dis 2010; 11 (03) 148-160
  • 139 Rossum LG et al. Colorectal cancer screening comparing no screening, immunochemical and guaiac fecal occult blood tests: a cost-effectiveness analysis. Int J Cancer 2011; 128 (08) 1908-1917
  • 140 Hundt S, Haug U, Brenner H. Comparative evaluation of immunochemical fecal occult blood tests for colorectal adenoma detection. Ann Intern Med 2009; 150 (03) 162-169
  • 141 Brenner H, Haug U, Hundt S. Inter-test agreement and quantitative cross-validation of immunochromatographical fecal occult blood tests. Int J Cancer 2010; 127 (07) 1643-1649
  • 142 Haug U, Hundt S, Brenner H. Quantitative immunochemical fecal occult blood testing for colorectal adenoma detection: evaluation in the target population of screening and comparison with qualitative tests. Am J Gastroenterol 2010; 105 (03) 682-690
  • 143 Allison JE et al. Screening for colorectal neoplasms with new fecal occult blood tests: update on performance characteristics. J Natl Cancer Inst 2007; 99 (19) 1462-1470
  • 144 Park DI et al. Comparison of guaiac-based and quantitative immunochemical fecal occult blood testing in a population at average risk undergoing colorectal cancer screening. Am J Gastroenterol 2010; 105 (09) 2017-2025
  • 145 Launoy GD et al. Evaluation of an immunochemical fecal occult blood test with automated reading in screening for colorectal cancer in a general average-risk population. Int J Cancer 2005; 115 (03) 493-496
  • 146 Roon AH et al. Diagnostic yield improves with collection of 2 samples in fecal immunochemical test screening without affecting attendance. Clin Gastroenterol Hepatol 2011; 9 (04) 333-339
  • 147 Doran J, Hardcastle JD. Bleeding patterns in colorectal cancer: the effect of aspirin and the implications for faecal occult blood testing. Br J Surg 1982; 69 (12) 711-713
  • 148 Ahlquist DA et al. Patterns of occult bleeding in asymptomatic colorectal cancer. Cancer 1989; 63 (09) 1826-1830
  • 149 Macrae FA, St JohnDJ. Relationship between patterns of bleeding and hemoccult sensitivity in patients with colorectal cancers or adenomas. Gastroenterology 1982; 82: 891-898
  • 150 Greegor DH. Occult blood testing for detection of asymptomatic colon cancer. Cancer 1971; 28: 131-134
  • 151 Hardcastle JD et al. Randomised controlled trial of faecal-occult-blood screening for colorectal cancer. Lancet 1996; 348 (9040) 1472-1477
  • 152 Kronborg O et al. Randomised study of screening for colorectal cancer with faecal-occult-blood test. Lancet 1996; 348 (9040) 1467-1471
  • 153 Hewitson P et al. Screening for colorectal cancer using the faecal occult blood test, Hemoccult. Cochrane Database Syst Rev 2007; 1: CD001216
  • 154 Levin B, Hess K, Johnson C et al. A comparison of 3 fecal occult blood tests. Arch Intern Med 1997; 157 (09) 970-976
  • 155 Gnauck R, Macrae FA, Fleisher M. How to perform the fecal occult blood test. CA Cancer J Clin 1984; 34: 134-147
  • 156 Jaffe RM et al. False-negative stool occult blood tests caused by ingestion of ascorbic acid (vitamin C). Ann Intern Med 1975; 83 (06) 824-826
  • 157 Macrae FA et al. Optimal dietary conditions for hemoccult testing. Gastroenterology 1982; 82 (05) 899-903
  • 158 Rozen P, Knaani J, Samuel Z. Eliminating the need for dietary restrictions when using a sensitive guaiac fecal occult blood test. Dig Dis Sci 1999; 44 (04) 756-760
  • 159 Pignone M et al. Meta-analysis of dietary restriction during fecal occult blood testing. Eff Clin Pract 2001; 4 (04) 150-156
  • 160 Rossum LG et al. Random comparison of guaiac and immunochemical fecal occult blood tests for colorectal cancer in a screening population. Gastroenterology 2008; 135 (01) 82-90
  • 161 Webendorfer S et al. Precautions for intestinal cancer in the workplace. An initiative for secondary prevention in the BASF joint-stock company. Dtsch Med Wochenschr 2004; 129 (06) 239-243
  • 162 Mandel JS et al. The effect of fecal occult-blood screening on the incidence of colorectal cancer. N Engl J Med 2000; 343 (22) 1603-1607
  • 163 Traverso G et al. Detection of APC mutations in fecal DNA from patients with colorectal tumors. N Engl J Med 2002; 346 (05) 311-320
  • 164 Ahlquist DA et al. Colorectal cancer screening by detection of altered human DNA in stool: feasibility of a multitarget assay panel. Gastroenterology 2000; 119 (05) 1219-1227
  • 165 Dong SM et al. Detecting colorectal cancer in stool with the use of multiple genetic targets. J Natl Cancer Inst 2001; 93 (11) 858-865
  • 166 Tagore KS et al. Sensitivity and specificity of a stool DNA multitarget assay panel for the detection of advanced colorectal neoplasia. Clin Colorectal Cancer 2003; 3 (01) 47-53
  • 167 Imperiale TF et al. Fecal DNA versus fecal occult blood for colorectal-cancer screening in an average-risk population. N Engl J Med 2004; 351 (26) 2704-2714
  • 168 Ahlquist DA et al. Stool DNA and occult blood testing for screen detection of colorectal neoplasia. Ann Intern Med 2008; 149 (07) 441-450 , W81
  • 169 Haug U, Hundt S, Brenner H. Sensitivity and specificity of faecal tumour M2 pyruvate kinase for detection of colorectal adenomas in a large screening study. Br J Cancer 2008; 99 (01) 133-135
  • 170 Moslein G et al. Analysis of the statistical value of various commercially available stool tests – a comparison of one stool sample in correlation to colonoscopy. Dtsch Med Wochenschr 2010; 135 (12) 557-562
  • 171 Haan MC et al. Diagnostic value of CT-colonography as compared to colonoscopy in an asymptomatic screening population: a meta-analysis. Eur Radiol 2011; 21 (08) 1747-1763
  • 172 El-Maraghi RH, Kielar AZ. CT colonography versus optical colonoscopy for screening asymptomatic patients for colorectal cancer a patient, intervention, comparison, outcome (PICO) analysis. Acad Radiol 2009; 16 (05) 564-571
  • 173 Pox CP, Schmiegel W. Role of CT colonography in colorectal cancer screening: risks and benefits. Gut 2010; 59 (05) 692-700
  • 174 Frazier AL et al. Cost-effectiveness of screening for colorectal cancer in the general population. Jama 2000; 284 (15) 1954-1961
  • 175 Geul KW et al. Prevention of colorectal cancer. Costs and effectiveness of sigmoidoscopy. Scand J Gastroenterol Suppl 1997; 223: 79-87
  • 176 Inadomi JM. Update on the cost-effectiveness of screening for colorectal neoplasia. Curr Opin Gastroenterol 2003; 29: 44-50
  • 177 Khandker RK et al. A decision model and cost-effectiveness analysis of colorectal cancer screening and surveillance guidelines for average-risk adults. Int J Technol Assess Health Care 2000; 16 (03) 799-810
  • 178 McGrath JS, Ponich TP, Gregor JC. Screening for colorectal cancer: the cost to find an advanced adenoma. Am J Gastroenterol 2002; 97 (11) 2902-2907
  • 179 Norum J. Prevention of colorectal cancer: a cost-effectiveness approach to a screening model employing sigmoidoscopy. Ann Oncol 1998; 9 (06) 613-618
  • 180 Pignone M et al. Cost-effectiveness analyses of colorectal cancer screening: a systematic review for the U. S. Preventive Services Task Force. Ann Intern Med 2002; 137 (02) 96-104
  • 181 Sonnenberg A, Delco F. Cost-effectiveness of a single colonoscopy in screening for colorectal cancer. Arch Intern Med 2002; 162 (02) 163-168
  • 182 Vijan S et al. Which colon cancer screening test? A comparison of costs, effectiveness, and compliance. Am J Med 2001; 111 (08) 593-601
  • 183 Zauber AG et al. Evaluating test strategies for colorectal cancer screening: a decision analysis for the U. S. Preventive Services Task Force. Ann Intern Med 2008; 149 (09) 659-669
  • 184 Lansdorp-Vogelaar I, Knudsen AB, Brenner H. Cost-effectiveness of colorectal cancer screening. Epidemiol Rev 2011; 33 (01) 88-100
  • 185 Sung JJ et al. Asia Pacific consensus recommendations for colorectal cancer screening. Gut 2008; 57 (08) 1166-1176
  • 186 Jasperson KW et al. Hereditary and familial colon cancer. Gastroenterology 2010; 138 (06) 2044-2058
  • 187 Andrieu N et al. Familial relative risk of colorectal cancer: a population-based study. Eur J Cancer 2003; 39 (13) 1904-1911
  • 188 Johns LE, Houlston RS. A systematic review and meta-analysis of familial colorectal cancer risk. Am J Gastroenterol 2001; 96 (10) 2992-3003
  • 189 Lichtenstein P et al. Environmental and heritable factors in the causation of cancer – analyses of cohorts of twins from Sweden, Denmark, and Finland. N Engl J Med 2000; 343 (02) 78-85
  • 190 Slattery ML et al. Family history and colorectal cancer: predictors of risk. Cancer Causes Control 2003; 14 (09) 879-887
  • 191 Winawer S et al. Colorectal cancer screening and surveillance: clinical guidelines and rationale-Update based on new evidence. Gastroenterology 2003; 124 (02) 544-560
  • 192 Bonelli L et al. Family history of colorectal cancer as a risk factor for benign and malignant tumours of the large bowel. A case-control study. Int J Cancer 1988; 41 (04) 513-517
  • 193 Fuchs CS et al. A prospective study of family history and the risk of colorectal cancer. N Engl J Med 1994; 331 (25) 1669-1674
  • 194 Guillem JG et al. Clustering of colorectal cancer in families of probands under 40 years of age. Dis Colon Rectum 1996; 39 (09) 1004-1007
  • 195 Guillem JG et al. Colonoscopic screening for neoplasms in asymptomatic first-degree relatives of colon cancer patients. A controlled, prospective study. Dis Colon Rectum 1992; 35 (06) 523-9
  • 196 Kune GA, Kune S, Watson LF. The role of heredity in the etiology of large bowel cancer: data from the Melbourne Colorectal Cancer Study. World J Surg 1989; 13 (01) 124-129
  • 197 Rozen P et al. Family history of colorectal cancer as a marker of potential malignancy within a screening programm. Cancer 1987; 60 (02) 248-254
  • 198 Sondergaard JO, Bulow S, Lynge E. Cancer incidence among parents of patients with colorectal cancer. Int J Cancer 1991; 47 (02) 202-206
  • 199 St John DJ et al. Cancer risk in relatives of patients with common colorectal cancer. Ann Int Med 1993; 118 (10) 785-790
  • 200 Butterworth AS, Higgins JP, Pharoah P. Relative and absolute risk of colorectal cancer for individuals with a family history: a meta-analysis. Eur J Cancer 2006; 42 (02) 216-227
  • 201 Hall NR et al. Hereditary susceptibility to colorectal cancer. Relatives of early onset cases are particularly at risk. Dis Colon Rectum 1996; 39 (07) 739-743
  • 202 Hunt LM et al. Endoscopic screening of relatives of patients with colorectal cancer. Gut 1998; 42 (01) 71-75
  • 203 Winawer SJ et al. Risk of colorectal cancer in the families of patients with adenomatous polyps. National Polyp Study Workgroup. N Engl J Med 1996; 334 (02) 82-87
  • 204 Ahsan H et al. Family history of colorectal adenomatous polyps and increased risk for colorectal cancer. Ann Intern Med 1998; 128 (11) 900-905
  • 205 Nakama H et al. Family history of colorectal adenomatous polyps as a risk factor for colorectal cancer. Eur J Cancer 2000; 36 (16) 2111-2114
  • 206 Almendingen K, Hofstad B, Vatn MH. Does a family history of cancer increase the risk of occurrence, growth, and recurrence of colorectal adenomas?. Gut 2003; 52 (05) 747-751
  • 207 Winawer SJ et al. Risk and surveillance of individuals with colorectal polyps. WHO Collaborating Centre for the Prevention of Colorectal Cancer. Bull World Health Organ 1990; 68 (06) 789-795
  • 208 Atkin WS, Morson BC, Cuzick J. Long-term risk of colorectal cancer after excision of rectosigmoid adenomas. N Engl J Med 1992; 326 (10) 658-662
  • 209 Otchy DP et al. Metachronous colon cancer in persons who have had a large adenomatous polyp. Am J Gastroenterol 1996; 91 (03) 448-454
  • 210 Stolck RU et al. Adenoma characteristics at first colonoscopy as predictors of adenoma recurrence and characteristics at follow-up. The Polyp Prevention Study Group. Gastroenterology 1998; 115 (01) 13-18
  • 211 Noshirwani KC et al. Adenoma size and number are predictive of adenoma recurrence: implications for surveillance colonoscopy. Gastrointest Endosc 2000; 51: 433-437
  • 212 Aldridge AJ, Simson JN. Histological assessment of colorectal adenomas by size. Are polyps less than 10 mm in size clinically important?. Eur J Surg 2001; 167 (10) 777-781
  • 213 Avidan B et al. New occurrence and recurrence of neoplasms within 5 years of a screening colonoscopy. Am J Gastroenterol 2002; 97 (06) 1524-1529
  • 214 Bertario L et al. Predictors of metachronous colorectal neoplasms in sporadic adenoma patients. Int J Cancer 2003; 105 (01) 82-87
  • 215 Chen CD et al. A case-cohort study for the disease natural history of adenoma-carcinoma and de novo carcinoma and surveillance of colon and rectum after polypectomy: implication for efficacy of colonoscopy. Br J Cancer 2003; 88 (12) 1866-1873
  • 216 Bensen S et al. The colonoscopic miss rate and true one-year recurrence of colorectal neoplastic polyps. Polyp Prevention Study Group. Am J Gastroenterol 1999; 94 (01) 194-199
  • 217 Katalinic A, Raspe H, Waldmann A. Positive family history of colorectal cancer – use of a questionnaire. Z Gastroenterol 2009; 47 (11) 1125-1131
  • 218 Baron JA et al. Neoplastic and antineoplastic effects of beta-carotene on colorectal adenoma recurrence: results of a randomized trial. J Natl Cancer Inst 2003; 95 (10) 717-722
  • 219 Karnes WE. Epidemiology and etiology of sporadic colorectal adenocarcinoma. Current opinion in Gastroenterology 1994; 10: 19-26
  • 220 Sandler RS et al. A randomized trial of aspirin to prevent colorectal adenomas in patients with previous colorectal cancer. N Engl J Med 2003; 348 (10) 883-890
  • 221 Rothwell PM et al. Long-term effect of aspirin on colorectal cancer incidence and mortality: 20-year follow-up of five randomised trials. Lancet 2010; 376 (9754) 1741-1750
  • 222 Burt RW. Screening of patients with a positive family history of colorectal cancer. Gastrointest Endosc Clin N Am 1997; 7 (01) 65-79
  • 223 Gilbert JM et al. Feasibility study of colonoscopy as the primary screening investigation in relatives of patients with colorectal cancer. Ann R Coll Surg Engl 2001; 83 (06) 415-419
  • 224 Syrigos KN et al. Colonoscopy in asymptomatic individuals with a family history of colorectal cancer. Ann Surg Oncol 2002; 9 (05) 439-443
  • 225 Bradshaw N et al. Colonoscopy surveillance of individuals at risk of familial colorectal cancer. Gut 2003; 52 (12) 1748-1751
  • 226 Brenner H, Hoffmeister M, Haug U. Family history and age at initiation of colorectal cancer screening. Am J Gastroenterol 2008; 103 (09) 2326-2331
  • 227 Waldmann A, Raspe H, Katalinic A. Colon cancer risk in persons at familial or hereditary risk aged < 55 years. Z Gastroenterol 2009; 47 (10) 1052-1058
  • 228 Levin B et al. Screening and surveillance for the early detection of colorectal cancer and adenomatous polyps, 2008: a joint guideline from the American Cancer Society, the US Multi-Society Task Force on Colorectal Cancer, and the American College of Radiology. Gastroenterology 2008; 134 (05) 1570-1595
  • 229 Engel C et al. Efficacy of annual colonoscopic surveillance in individuals with hereditary nonpolyposis colorectal cancer. Clin Gastroenterol Hepatol 2010; 8 (02) 174-182
  • 230 Dove-Edwin I et al. Prevention of colorectal cancer by colonoscopic surveillance in individuals with a family history of colorectal cancer: 16 year, prospective, follow-up study. BMJ 2005; 331 (7524) 1047
  • 231 Duncan RE et al. The challenge of developmentally appropriate care: predictive genetic testing in young people for familial adenomatous polyposis. Fam Cancer 2010; 9 (01) 27-35
  • 232 Douma KF et al. Psychosocial issues in genetic testing for familial adenomatous polyposis: a review of the literature. Psychooncology 2008; 17 (08) 737-745
  • 233 Douma KF et al. Psychological distress and use of psychosocial support in familial adenomatous polyposis. Psychooncology 2010; 19 (03) 289-298
  • 234 Vasen HF et al. The International Collaborative Group on Hereditary Non-Polyposis Colorectal Cancer (ICG-HNPCC). Dis Colon Rectum 1991; 34 (05) 424-425
  • 235 Rodriguez-Bigas MA et al. A National Cancer Institute Workshop on Hereditary Nonpolyposis Colorectal Cancer Syndrome: meeting highlights and Bethesda guidelines. J Natl Cancer Inst 1997; 89 (23) 1758-1762
  • 236 Schulmann K et al. Small bowel cancer risk in Lynch syndrome. Gut 2008; 57 (11) 1629-1630
  • 237 Kate GL et al. Is surveillance of the small bowel indicated for Lynch syndrome families?. Gut 2007; 56 (09) 1198-1201
  • 238 Schulmann K et al. HNPCC-associated small bowel cancer: clinical and molecular characteristics. Gastroenterology 2005; 128 (03) 590-599
  • 239 der Post RS et al. Risk of urothelial bladder cancer in Lynch syndrome is increased, in particular among MSH2 mutation carriers. J Med Genet 2010; 47 (07) 464-470
  • 240 Kastrinos F et al. Risk of pancreatic cancer in families with Lynch syndrome. JAMA 2009; 302 (16) 1790-1795
  • 241 Win AK et al. Colorectal and Other Cancer Risks for Carriers and Noncarriers From Families With a DNA Mismatch Repair Gene Mutation: A Prospective Cohort Study. J Clin Oncol 2012; 30: 958-964
  • 242 Vasen HF et al. MSH2 mutation carriers are at higher risk of cancer than MLH1 mutation carriers: a study of hereditary nonpolyposis colorectal cancer families. J Clin Oncol 2001; 19 (20) 4074-4080
  • 243 Aarnio M et al. Life-time risk of different cancers in hereditary non-polyposis colorectal cancer (HNPCC) syndrome. Int J Cancer 1995; 64 (06) 430-433
  • 244 Vasen HF et al. The risk of brain tumours in hereditary non-polyposis colorectal cancer (HNPCC). Int J Cancer 1996; 65 (04) 422-425
  • 245 Kruse R et al. Muir-Torre phenotype has a frequency of DNA mismatch-repair-gene mutations similar to that in hereditary nonpolyposis colorectal cancer families defined by the Amsterdam criteria. Am J Hum Genet 1998; 63 (01) 63-70
  • 246 Umar A et al. Revised Bethesda Guidelines for hereditary nonpolyposis colorectal cancer (Lynch syndrome) and microsatellite instability. J Natl Cancer Inst 2004; 96 (04) 261-268
  • 247 Shia J. Immunohistochemistry versus microsatellite instability testing for screening colorectal cancer patients at risk for hereditary nonpolyposis colorectal cancer syndrome. Part I. The utility of immunohistochemistry. J Mol Diagn 2008; 10 (04) 293-300
  • 248 Deng G et al. BRAF mutation is frequently present in sporadic colorectal cancer with methylated hMLH1, but not in hereditary nonpolyposis colorectal cancer. Clin Cancer Res 2004; 10 (01) 191-195
  • 249 Domingo E et al. BRAF screening as a low-cost effective strategy for simplifying HNPCC genetic testing. J Med Genet 2004; 41 (09) 664-668
  • 250 Loughrey MB et al. Incorporation of somatic BRAF mutation testing into an algorithm for the investigation of hereditary non-polyposis colorectal cancer. Fam Cancer 2007; 6 (03) 301-310
  • 251 McGivern A et al. Promoter hypermethylation frequency and BRAF mutations distinguish hereditary non-polyposis colon cancer from sporadic MSI-H colon cancer. Fam Cancer 2004; 3 (02) 101-107
  • 252 Levine AJ et al. Cancer risks for the relatives of colorectal cancer cases with a methylated MLH1 promoter region: data from the Colorectal Cancer Family Registry. Cancer Prev Res (Phila) 2012; 5 (02) 328-335
  • 253 Foulkes WD. A tale of four syndromes: familial adenomatous polyposis, Gardner syndrome, attenuated APC and Turcot syndrome. QJM 1995; 88 (12) 853-863
  • 254 Lynch HT et al. Attenuated familial adenomatous polyposis (AFAP). A phenotypically and genotypically distinctive variant of FAP. Cancer 1995; 76 (12) 2427-2433
  • 255 Lynch HT, Smyrk TC. Classification of familial adenomatous polyposis: a diagnostic nightmare. Am J Hum Genet 1998; 62 (06) 1288-1289
  • 256 Soravia C et al. Genotype-phenotype correlations in attenuated adenomatous polyposis coli. Am J Hum Genet 1998; 62: 1290-1301
  • 257 Hernegger GS, Moore HG, Guillem JG. Attenuated familial adenomatous polyposis: an evolving and poorly understood entity. Dis Colon Rectum 2002; 45 (01) 127-134 ; discussion 134-136
  • 258 Knudsen AL, Bisgaard ML, Bulow S. Attenuated familial adenomatous polyposis (AFAP). A review of the literature. Fam Cancer 2003; 2 (01) 43-55
  • 259 Al-Tassan N et al. Inherited variants of MYH associated with somatic G:C → T:A mutations in colorectal tumors. Nat Genet 2002; 30 (02) 227-232
  • 260 Cao Y et al. Challenge in the differentiation between attenuated familial adenomatous polyposis and hereditary nonpolyposis colorectal cancer: case report with review of the literature. Am J Gastroenterol 2002; 97 (07) 1822-1827
  • 261 Aretz S. The differential diagnosis and surveillance of hereditary gastrointestinal polyposis syndromes. Dtsch Arztebl Int 2010; 107 (10) 163-173
  • 262 Aretz S, Genuardi M, Hes FJ. Clinical utility gene card for: MUTYH-associated polyposis (MAP), autosomal recessive colorectal adenomatous polyposis. Eur J Hum Genet 2013; 21
  • 263 Sampson JR, Jones N. MUTYH-associated polyposis. Best Pract Res Clin Gastroenterol 2009; 23 (02) 209-218
  • 264 Morreau H, Riddel R, Aretz S. MUTYH-associated polyposis. In: Bosman FT, et al. Editors WHO Classification of Tumours of the Digestive System. Lyon: IARC/WHO Press; 2010: 156-159
  • 265 Aretz S et al. MUTYH-associated polyposis: 70 of 71 patients with biallelic mutations present with an attenuated or atypical phenotype. Int J Cancer 2006; 119 (04) 807-814
  • 266 Lubbe SJ et al. Clinical implications of the colorectal cancer risk associated with MUTYH mutation. J Clin Oncol 2009; 27 (24) 3975-3980
  • 267 Cleary SP et al. Germline MutY human homologue mutations and colorectal cancer: a multisite case-control study. Gastroenterology 2009; 136 (04) 1251-1260
  • 268 Boparai KS et al. Hyperplastic polyps and sessile serrated adenomas as a phenotypic expression of MYH-associated polyposis. Gastroenterology 2008; 135 (06) 2014-2018
  • 269 Vogt S et al. Expanded extracolonic tumor spectrum in MUTYH-associated polyposis. Gastroenterology 2009; 137 (06) 1976-1985
  • 270 Papadopoulos N, Lindblom A. Molecular basis of HNPCC: mutations of MMR genes. Hum Mut 1997; 10: 89-99
  • 271 Kuiper RP et al. Recurrence and variability of germline EPCAM deletions in Lynch syndrome. Hum Mutat 2011; 32 (04) 407-414
  • 272 Jarvinen HJ et al. Controlled 15-year trial on screening for colorectal cancer in families with hereditary nonpolyposis colorectal cancer. Gastroenterology 2000; 118 (05) 829-834
  • 273 Vos tot Nederveen Cappel WH et al. Surveillance for hereditary nonpolyposis colorectal cancer: a long-term study on 114 families. Dis Colon Rectum 2002; 45 (12) 1588-1594
  • 274 Edelstein DL et al. Rapid development of colorectal neoplasia in patients with Lynch syndrome. Clin Gastroenterol Hepatol 2011; 9 (04) 340-343
  • 275 Renkonen-Sinisalo L et al. Surveillance improves survival of colorectal cancer in patients with hereditary nonpolyposis colorectal cancer. Cancer Detect Prev 2000; 24 (02) 137-142
  • 276 Huneburg R et al. Chromocolonoscopy detects more adenomas than white light colonoscopy or narrow band imaging colonoscopy in hereditary nonpolyposis colorectal cancer screening. Endoscopy 2009; 41 (04) 316-322
  • 277 Stoffel EM et al. Missed adenomas during colonoscopic surveillance in individuals with Lynch Syndrome (hereditary nonpolyposis colorectal cancer). Cancer Prev Res (Phila) 2008; 1 (06) 470-475
  • 278 Hurlstone DP et al. High magnification chromoscopic colonoscopy or high frequency 20 MHz mini probe endoscopic ultrasound staging for early colorectal neoplasia: a comparative prospective analysis. Gut 2005; 54 (11) 1585-1589
  • 279 Aarnio M et al. Cancer risk in mutation carriers of DNA-mismatch-repair genes. Int J Cancer 1999; 81 (02) 214-218
  • 280 Dove-Edwin I et al. The outcome of endometrial carcinoma surveillance by ultrasound scan in women at risk of hereditary nonpolyposis colorectal carcinoma and familial colorectal carcinoma. Cancer 2002; 94 (06) 1708-1712
  • 281 Rijcken FE et al. Gynecologic screening in hereditary nonpolyposis colorectal cancer. Gynecol Oncol 2003; 91 (01) 74-80
  • 282 Renkonen-Sinisalo L et al. Surveillance for endometrial cancer in hereditary nonpolyposis colorectal cancer syndrome. Int J Cancer 2007; 120 (04) 821-824
  • 283 Vasen HF et al. Guidelines for the clinical management of Lynch syndrome (hereditary non-polyposis cancer). J Med Genet 2007; 44 (06) 353-362
  • 284 Goecke T et al. Genotype-phenotype comparison of German MLH1 and MSH2 mutation carriers clinically affected with Lynch syndrome: a report by the German HNPCC Consortium. J Clin Oncol 2006; 24 (26) 4285-4292
  • 285 Burn J et al. Effect of aspirin or resistant starch on colorectal neoplasia in the Lynch syndrome. N Engl J Med 2008; 359 (24) 2567-2578
  • 286 Burn J et al. Long-term effect of aspirin on cancer risk in carriers of hereditary colorectal cancer: an analysis from the CAPP2 randomised controlled trial. Lancet 2011; 378 (9809) 2081-2087
  • 287 Natarajan N et al. Comparison of extended colectomy and limited resection in patients with Lynch syndrome. Dis Colon Rectum 2010; 53 (01) 77-82
  • 288 Kalady MF et al. Risk of colorectal adenoma and carcinoma after colectomy for colorectal cancer in patients meeting Amsterdam criteria. Ann Surg 2010; 252 (03) 507-511 ; discussion 511-513
  • 289 Parry S et al. Metachronous colorectal cancer risk for mismatch repair gene mutation carriers: the advantage of more extensive colon surgery. Gut 2011; 60 (07) 950-957
  • 290 Stupart DA et al. Surgery for colonic cancer in HNPCC: total vs. segmental colectomy. Colorectal Dis 2011; 13 (12) 1395-1399
  • 291 Schmeler KM et al. Prophylactic surgery to reduce the risk of gynecologic cancers in the Lynch syndrome. N Engl J Med 2006; 354 (03) 261-269
  • 292 Church JM et al. Teenagers with familial adenomatous polyposis: what is their risk for colorectal cancer?. Dis Colon Rectum 2002; 45 (07) 887-889
  • 293 King JE et al. Care of patients and their families with familial adenomatous polyposis. Mayo Clin Proc 2000; 75 (01) 57-67
  • 294 Bertario L et al. Causes of death and postsurgical survival in familial adenomatous polyposis: results from the Italian Registry. Italian Registry of Familial Polyposis Writing Committee. Semin Surg Oncol 1994; 10 (03) 225-234
  • 295 Galle TS, Juel K, Bulow S. Causes of death in familial adenomatous polyposis. Scand J Gastroenterol 1999; 34 (08) 808-812
  • 296 Heiskanen I, Luostarinen T, Jarvinen HJ. Impact of screening examinations on survival in familial adenomatous polyposis. Scand J Gastroenterol 2000; 35 (12) 1284-1287
  • 297 Vasen HF et al. Decision analysis in the surgical treatment of patients with familial adenomatous polyposis: a Dutch-Scandinavian collaborative study including 659 patients. Gut 2001; 49 (02) 231-235
  • 298 Bulow S. Results of national registration of familial adenomatous polyposis. Gut 2003; 52 (05) 742-746
  • 299 Ficari F et al. APC gene mutations and colorectal adenomatosis in familial adenomatous polyposis. Br J Cancer 2000; 82 (02) 348-353
  • 300 Bulow S. Clinical features in familial polyposis coli. Results of the Danish Polyposis Register. Dis Colon Rectum 1986; 29 (02) 102-107
  • 301 De Cosse JJ et al. Rectal cancer risk in patients treated for familial adenomatous polyposis. The Leeds Castle Polyposis Group. Br J Surg 1992; 79 (12) 1372-1375
  • 302 Nyam DC et al. Ileal pouch-anal canal anastomosis for familial adenomatous polyposis: early and late results. Ann Surg 1997; 226 (04) 514-519 ; discussion 519-521
  • 303 Parc YR et al. Familial adenomatous polyposis: results after ileal pouch-anal anastomosis in teenagers. Dis Colon Rectum 2000; 43 (07) 893-898 ; discussion 898-902
  • 304 Van Duijvendijk P et al. Quality of life after total colectomy with ileorectal anastomosis or proctocolectomy and ileal pouch-anal anastomosis for familial adenomatous polyposis. Br J Surg 2000; 87 (05) 590-596
  • 305 Church J et al. Risk of rectal cancer in patients after colectomy and ileorectal anastomosis for familial adenomatous polyposis: a function of available surgical options. Dis Colon Rectum 2003; 46 (09) 1175-1181
  • 306 Will OC et al. Familial adenomatous polyposis and the small bowel: a loco-regional review and current management strategies. Pathol Res Pract 2008; 204 (07) 449-458
  • 307 Spigelman AD et al. Upper gastrointestinal cancer in patients with familial adenomatous polyposis. Lancet 1989; 2 (8666) 783-785
  • 308 Burke CA et al. The natural history of untreated duodenal and ampullary adenomas in patients with familial adenomatous polyposis followed in an endoscopic surveillance program. Gastrointest Endosc 1999; 49 (03) 358-364
  • 309 Matsumoto T et al. Natural history of ampullary adenoma in familial adenomatous polyposis: reconfirmation of benign nature during extended surveillance. Am J Gastroenterol 2000; 95 (06) 1557-1562
  • 310 Moozar KL et al. Slow progression of periampullary neoplasia in familial adenomatous polyposis. J Gastrointest Surg 2002; 6 (06) 831-837 ; discussion 837
  • 311 Saurin JC et al. The influence of mutation site and age on the severity of duodenal polyposis in patients with familial adenomatous polyposis. Gastrointest Endosc 2002; 55 (03) 342-347
  • 312 Saurin JC et al. Surveillance of duodenal adenomas in familial adenomatous polyposis reveals high cumulative risk of advanced disease. J Clin Oncol 2004; 22 (03) 493-498
  • 313 Vasen HF et al. Decision analysis in the management of duodenal adenomatosis in familial adenomatous polyposis. Gut 1997; 40: 716-719
  • 314 Bulow S et al. Duodenal adenomatosis in familial adenomatous polyposis. Gut 2004; 53 (03) 381-386
  • 315 Kadmon M, Tandara A, Herfarth C. Duodenal adenomatosis in familial adenomatous polyposis coli. A review of the literature and results from the Heidelberg Polyposis Register. Int J Colorectal Dis 2001; 16 (02) 63-75
  • 316 Norton ID et al. Safety and outcome of endoscopic snare excision of the major duodenal papilla. Gastrointest Endosc 2002; 56 (02) 239-243
  • 317 Kalady MF et al. Pancreas-preserving duodenectomy in the management of duodenal familial adenomatous polyposis. J Gastrointest Surg 2002; 6 (01) 82-87
  • 318 Parc Y, Mabrut JY, Shields C. Surgical management of the duodenal manifestations of familial adenomatous polyposis. Br J Surg 2011; 98 (04) 480-484
  • 319 Vos tot Nederveen Cappel WH et al. Worldwide survey among polyposis registries of surgical management of severe duodenal adenomatosis in familial adenomatous polyposis. Br J Surg 2003; 90 (06) 705-710
  • 320 Heiskanen I, Kellokumpu I, Jarvinen H. Management of duodenal adenomas in 98 patients with familial adenomatous polyposis. Endoscopy 1999; 31 (06) 412-416
  • 321 Norton ID et al. Endoscopic surveillance and ablative therapy for periampullary adenomas. Am J Gastroenterol 2001; 96 (01) 101-106
  • 322 Bleau BL, Gostout CJ. Endoscopic treatment of ampullary adenomas in familial adenomatous polyposis. J Clin Gastroenterol 1996; 22 (03) 237-241
  • 323 Soravia C et al. Desmoid disease in patients with familial adenomatous polyposis. Dis Colon Rectum 2000; 43 (03) 363-369
  • 324 Bertario L et al. Multiple approach to the exploration of genotype-phenotype correlations in familial adenomatous polyposis. J Clin Oncol 2003; 21 (09) 1698-1707
  • 325 Friedl W et al. Can APC mutation analysis contribute to therapeutic decisions in familial adenomatous polyposis? Experience from 680 FAP families. Gut 2001; 48 (04) 515-521
  • 326 Janinis J et al. The pharmacological treatment of aggressive fibromatosis: a systematic review. Ann Oncol 2003; 14 (02) 181-190
  • 327 Tonelli F et al. Treatment of desmoids and mesenteric fibromatosis in familial adenomatous polyposis with raloxifene. Tumori 2003; 89 (04) 391-396
  • 328 Gega M et al. Successful chemotherapeutic modality of doxorubicin plus dacarbazine for the treatment of desmoid tumors in association with familial adenomatous polyposis. J Clin Oncol 2006; 24 (01) 102-105
  • 329 Skapek SX et al. Vinblastine and methotrexate for desmoid fibromatosis in children: results of a Pediatric Oncology Group Phase II Trial. J Clin Oncol 2007; 25 (05) 501-506
  • 330 Latchford AR et al. A 10-year review of surgery for desmoid disease associated with familial adenomatous polyposis. Br J Surg 2006; 93 (10) 1258-1264
  • 331 Möslein G. Current ideas in desmoid tumours: invited commentary. Fam Cancer 2006; 5: 287-288
  • 332 Clark SK, Phillips RK. Desmoids in familial adenomatous polyposis. Br J Surg 1996; 83 (11) 1494-1504
  • 333 Nieuwenhuis MH et al. Evaluation of management of desmoid tumours associated with familial adenomatous polyposis in Dutch patients. Br J Cancer 2011; 104 (01) 37-42
  • 334 Huang K et al. Prognostic factors for extra-abdominal and abdominal wall desmoids: a 20-year experience at a single institution. J Surg Oncol 2009; 100 (07) 563-569
  • 335 Salas S et al. Prognostic factors influencing progression-free survival determined from a series of sporadic desmoid tumors: a wait-and-see policy according to tumor presentation. J Clin Oncol 2011; 29 (26) 3553-3558
  • 336 Bulow C, Bulow S. Is screening for thyroid carcinoma indicated in familial adenomatous polyposis? The Leeds Castle Polyposis Group. Int J Colorectal Dis 1997; 12 (04) 240-242
  • 337 Jarrar AM et al. Screening for thyroid cancer in patients with familial adenomatous polyposis. Ann Surg 2011; 253 (03) 515-521
  • 338 Martayan A et al. Gene variants associated to malignant thyroid disease in familial adenomatous polyposis: a novel APC germline mutation. J Endocrinol Invest 2010; 33 (09) 603-606
  • 339 Herraiz M et al. Prevalence of thyroid cancer in familial adenomatous polyposis syndrome and the role of screening ultrasound examinations. Clin Gastroenterol Hepatol 2007; 5 (03) 367-373
  • 340 Bell B, Mazzaferri EL. Familial adenomatous polyposis (Gardner’s syndrome) and thyroid carcinoma. A case report and review of the literature. . Dig Dis Sci 1993; 38 (01) 185-190
  • 341 Perrier ND et al. Thyroid cancer in patients with familial adenomatous polyposis. World J Surg 1998; 22 (07) 738-742 ; discussion 743
  • 342 Hughes LJ, Michels VV. Risk of hepatoblastoma in familial adenomatous polyposis. Am J Med Genet 1992; 43 (06) 1023-1025
  • 343 Thomas D et al. Familial hepatoblastoma and APC gene mutations: renewed call for molecular research. Eur J Cancer 2003; 39 (15) 2200-2204
  • 344 Aretz S et al. Should children at risk for familial adenomatous polyposis be screened for hepatoblastoma and children with apparently sporadic hepatoblastoma be screened for APC germline mutations?. Pediatr Blood Cancer 2006; 47 (06) 811-818
  • 345 Vasen HF et al. Guidelines for the clinical management of familial adenomatous polyposis (FAP). Gut 2008; 57 (05) 704-713
  • 346 Waddell WR, Loughry RW. Sulindac for polyposis of the colon. J Surg Oncol 1983; 24 (01) 83-7
  • 347 Labayle D et al. Sulindac causes regression of rectal polyps in familial adenomatous polyposis. Gastroenterology 1991; 101 (03) 635-639
  • 348 Giardiello FM et al. Treatment of colonic and rectal adenomas with sulindac in familial adenomatous polyposis. N Engl J Med 1993; 328 (18) 1313-1316
  • 349 Cruz-Correa M et al. Long-term treatment with sulindac in familial adenomatous polyposis: a prospective cohort study. Gastroenterology 2002; 122 (03) 641-645
  • 350 Winde G et al. Complete reversion and prevention of rectal adenomas in colectomized patients with familial adenomatous polyposis by rectal low-dose sulindac maintenance treatment. Advantages of low-dose nonsteroidal anti-inflammatory drug regimen in reversing adenomas exceeding 33 months. Dis Colon Rectum 1995; 38 (08) 813-830
  • 351 Giardiello FM et al. Primary chemoprevention of familial adenomatous polyposis with sulindac. N Engl J Med 2002; 346 (14) 1054-1059
  • 352 Steinbach G et al. The effect of celecoxib, a cyclooxygenase-2 inhibitor, in familial adenomatous polyposis. N Engl J Med 2000; 342 (26) 1946-1952
  • 353 Phillips RK et al. A randomised, double blind, placebo controlled study of celecoxib, a selective cyclooxygenase 2 inhibitor, on duodenal polyposis in familial adenomatous polyposis. Gut 2002; 50 (06) 857-860
  • 354 Solomon SD et al. Cardiovascular risk of celecoxib in 6 randomized placebo-controlled trials: the cross trial safety analysis. Circulation 2008; 117 (16) 2104-2113
  • 355 Matsuo S et al. Attenuated familial adenomatous polyposis associated with advanced rectal cancer in a 16-year-old boy: report of a case. Surg Today 2001; 31 (11) 1020-1023
  • 356 Leggett BA et al. Severe upper gastrointestinal polyposis associated with sparse colonic polyposis in a familial adenomatous polyposis family with an APC mutation at codon 1520. Gut 1997; 41 (04) 518-521
  • 357 Zwick A et al. Gastric adenocarcinoma and dysplasia in fundic gland polyps of a patient with attenuated adenomatous polyposis coli. Gastroenterology 1997; 113 (02) 659-663
  • 358 Hofgartner WT et al. Gastric adenocarcinoma associated with fundic gland polyps in a patient with attenuated familial adenomatous polyposis. Am J Gastroenterol 1999; 94 (08) 2275-2281
  • 359 Jones N et al. Increased colorectal cancer incidence in obligate carriers of heterozygous mutations in MUTYH. Gastroenterology 2009; 137 (02) 489-494 , 494 e1; quiz 725-726
  • 360 Farrington SM et al. Germline susceptibility to colorectal cancer due to base-excision repair gene defects. Am J Hum Genet 2005; 77 (01) 112-119
  • 361 Nielsen M et al. Analysis of MUTYH genotypes and colorectal phenotypes in patients With MUTYH-associated polyposis. Gastroenterology 2009; 136 (02) 471-476
  • 362 Nascimbeni R et al. Rectum-sparing surgery may be appropriate for biallelic MutYH-associated polyposis. Dis Colon Rectum 2010; 53 (12) 1670-1675
  • 363 Nielsen M et al. Duodenal carcinoma in MUTYH-associated polyposis. J Clin Pathol 2006; 59 (11) 1212-1215
  • 364 Zbuk KM, Eng C. Hamartomatous polyposis syndromes. Nat Clin Pract Gastroenterol Hepatol 2007; 4 (09) 492-502
  • 365 Aretz S et al. High proportion of large genomic STK11 deletions in Peutz-Jeghers syndrome. Hum Mutat 2005; 26 (06) 513-519
  • 366 Hinds R et al. Complications of childhood Peutz-Jeghers syndrome: implications for pediatric screening. J Pediatr Gastroenterol Nutr 2004; 39 (02) 219-220
  • 367 Reid JD. Intestinal carcinoma in the Peutz-Jeghers syndrome. Jama 1974; 229 (07) 833-834
  • 368 Burdick D, Prior JT. Peutz-Jeghers syndrome. A clinicopathologic study of a large family with a 27-year follow-up. Cancer 1982; 50 (10) 2139-2146
  • 369 Giardiello FM et al. Increased risk of cancer in the Peutz-Jeghers syndrome. N Engl J Med 1987; 316 (24) 1511-1514
  • 370 Foley TR, McGarrity TJ, Abt AB. Peutz-Jeghers syndrome: a clinicopathologic survey of the “Harrisburg family” with a 49-year follow-up. Gastroenterology 1988; 95 (06) 1535-1540
  • 371 Spigelman AD, Murday V, Phillips RK. Cancer and the Peutz-Jeghers syndrome. Gut 1989; 30 (11) 1588-1590
  • 372 Hizawa K et al. Neoplastic transformation arising in Peutz-Jeghers polyposis. Dis Colon Rectum 1993; 36: 953-957
  • 373 Boardman LA et al. Increased risk for cancer in patients with the Peutz-Jeghers syndrome. Ann Intern Med 1998; 128 (11) 896-899
  • 374 Mehenni H et al. Cancer risks in LKB1 germline mutation carriers. Gut 2006; 55 (07) 984-990
  • 375 Giardiello FM et al. Very high risk of cancer in familial Peutz-Jeghers syndrome. Gastroenterology 2000; 119 (06) 1447-1453
  • 376 Hearle N et al. Frequency and spectrum of cancers in the Peutz-Jeghers syndrome. Clin Cancer Res 2006; 12 (10) 3209-3215
  • 377 Sweet K et al. Molecular classification of patients with unexplained hamartomatous and hyperplastic polyposis. JAMA 2005; 294 (19) 2465-2473
  • 378 Aretz S et al. High proportion of large genomic deletions and a genotype phenotype update in 80 unrelated families with juvenile polyposis syndrome. J Med Genet 2007; 44 (11) 702-709
  • 379 Gallione CJ et al. A combined syndrome of juvenile polyposis and hereditary haemorrhagic telangiectasia associated with mutations in MADH4 (SMAD4). Lancet 2004; 363 (9412) 852-859
  • 380 Watanabe A et al. Familial juvenile polyposis of the stomach. Gastroenterology 1979; 77 (01) 148-151
  • 381 Jass JR et al. Juvenile polyposis – a precancerous condition. Histopathology 1988; 13 (06) 619-630
  • 382 Sassatelli R et al. Generalized juvenile polyposis with mixed pattern and gastric cancer. Gastroenterology 1993; 104 (03) 910-915
  • 383 Coburn MC et al. Malignant potential in intestinal juvenile polyposis syndromes. Ann Surg Oncol 1995; 2 (05) 386-391
  • 384 Desai DC et al. Juvenile polyposis. Br J Surg 1995; 82 (01) 14-17
  • 385 Delnatte C et al. Contiguous gene deletion within chromosome arm 10q is associated with juvenile polyposis of infancy, reflecting cooperation between the BMPR1A and PTEN tumor-suppressor genes. Am J Hum Genet 2006; 78 (06) 1066-1074
  • 386 Hobert JA, Eng C. PTEN hamartoma tumor syndrome: an overview. Genet Med 2009; 11 (10) 687-694
  • 387 Tan MH et al. Lifetime cancer risks in individuals with germline PTEN mutations. Clin Cancer Res 2012; 18 (02) 400-407
  • 388 Orloff MS, Eng C. Genetic and phenotypic heterogeneity in the PTEN hamartoma tumour syndrome. Oncogene 2008; 27 (41) 5387-5397
  • 389 Marsh DJ et al. PTEN mutation spectrum and genotype-phenotype correlations in Bannayan-Riley-Ruvalcaba syndrome suggest a single entity with Cowden syndrome. Hum Mol Genet 1999; 8 (08) 1461-1472
  • 390 Jeevaratnam P et al. Familial giant hyperplastic polyposis predisposing to colorectal cancer: a new hereditary bowel cancer syndrome. J Pathol 1996; 179 (01) 20-25
  • 391 Leggett BA et al. Hyperplastic polyposis: association with colorectal cancer. Am J Surg Pathol 2001; 25 (02) 177-184
  • 392 Renaut AJ, Douglas PR, Newstead GL. Hyperplastic polyposis of the colon and rectum. Colorectal Dis 2002; 4 (03) 213-215
  • 393 Jaeger EE et al. An ancestral Ashkenazi haplotype at the HMPS/CRAC1 locus on 15q13-q14 is associated with hereditary mixed polyposis syndrome. Am J Hum Genet 2003; 72 (05) 1261-1267
  • 394 Rozen P, Samuel Z, Brazowski E. A prospective study of the clinical, genetic, screening, and pathologic features of a family with hereditary mixed polyposis syndrome. Am J Gastroenterol 2003; 98 (10) 2317-2320
  • 395 Beggs AD et al. Peutz-Jeghers syndrome: a systematic review and recommendations for management. Gut 2010; 59 (07) 975-986
  • 396 Dignass A et al. Updated German guideline on diagnosis and treatment of ulcerative colitis, 2011. Z Gastroenterol 2011; 49 (09) 1276-1341
  • 397 Collins PD et al. Strategies for detecting colon cancer and/or dysplasia in patients with inflammatory bowel disease. Cochrane Database Syst Rev 2006; 2: CD000279
  • 398 Rutter MD et al. Thirty-year analysis of a colonoscopic surveillance program for neoplasia in ulcerative colitis. Gastroenterology 2006; 130 (04) 1030-1038
  • 399 Lutgens MW et al. High frequency of early colorectal cancer in inflammatory bowel disease. Gut 2008; 57 (09) 1246-1251
  • 400 Lim CH et al. Ten year follow up of ulcerative colitis patients with and without low grade dysplasia. Gut 2003; 52 (08) 1127-1132
  • 401 Connell WR et al. Factors affecting the outcome of endoscopic surveillance for cancer in ulcerative colitis. Gastroenterology 1994; 107 (04) 934-944
  • 402 Claessen MM et al. More right-sided IBD-associated colorectal cancer in patients with primary sclerosing cholangitis. Inflamm Bowel Dis 2009; 15 (09) 1331-1336
  • 403 Soetikno RM et al. Increased risk of colorectal neoplasia in patients with primary sclerosing cholangitis and ulcerative colitis: a meta-analysis. Gastrointest Endosc 2002; 56 (01) 48-54
  • 404 Scarpa M et al. Systematic review of dysplasia after restorative proctocolectomy for ulcerative colitis. Br J Surg 2007; 94 (05) 534-545
  • 405 Hoffmann JC et al. Clinical practice guideline on diagnosis and treatment of Crohn’s disease. Z Gastroenterol 2008; 46 (09) 1094-1146
  • 406 Rex DK et al. Quality in the technical performance of colonoscopy and the continuous quality improvement process for colonoscopy: recommendations of the U. S. Multi-Society Task Force on Colorectal Cancer. Am J Gastroenterol 2002; 97 (06) 1296-1308
  • 407 Barclay RL et al. Colonoscopic withdrawal times and adenoma detection during screening colonoscopy. N Engl J Med 2006; 355 (24) 2533-2541
  • 408 Simmons DT et al. Impact of endoscopist withdrawal speed on polyp yield: implications for optimal colonoscopy withdrawal time. Aliment Pharmacol Ther 2006; 24 (06) 965-971
  • 409 Lieberman D. A call to action – measuring the quality of colonoscopy. N Engl J Med 2006; 355 (24) 2588-2589
  • 410 Pickhardt PJ et al. Computed tomographic virtual colonoscopy to screen for colorectal neoplasia in asymptomatic adults. N Engl J Med 2003; 349 (23) 2191-2200
  • 411 Robertson DJ et al. Colorectal cancer in patients under close colonoscopic surveillance. Gastroenterology 2005; 129 (01) 34-41
  • 412 Hosokawa O et al. Invasive colorectal cancer detected up to 3 years after a colonoscopy negative for cancer. Endoscopy 2003; 35 (06) 506-510
  • 413 Bressler B et al. Colonoscopic miss rates for right-sided colon cancer: a population-based analysis. Gastroenterology 2004; 127 (02) 452-456
  • 414 Leaper M et al. Reasons for failure to diagnose colorectal carcinoma at colonoscopy. Endoscopy 2004; 36 (06) 499-503
  • 415 Pabby A et al. Analysis of colorectal cancer occurrence during surveillance colonoscopy in the dietary Polyp Prevention Trial. Gastrointest Endosc 2005; 61 (03) 385-391
  • 416 Cotton PB et al. Computed tomographic colonography (virtual colonoscopy): a multicenter comparison with standard colonoscopy for detection of colorectal neoplasia. Jama 2004; 291 (14) 1713-1719
  • 417 Rockey DC et al. Analysis of air contrast barium enema, computed tomographic colonography, and colonoscopy: prospective comparison. Lancet 2005; 365 (9456) 305-311
  • 418 Halligan S et al. CT colonography in the detection of colorectal polyps and cancer: systematic review, meta-analysis, and proposed minimum data set for study level reporting. Radiology 2005; 237 (03) 893-904
  • 419 Mulhall BP, Veerappan GR, Jackson JL. Meta-analysis: computed tomographic colonography. Ann Intern Med 2005; 142 (08) 635-650
  • 420 Johnson CD et al. Comparison of the relative sensitivity of CT colonography and double-contrast barium enema for screen detection of colorectal polyps. Clin Gastroenterol Hepatol 2004; 2 (04) 314-321
  • 421 Purkayastha S et al. Magnetic resonance colonography versus colonoscopy as a diagnostic investigation for colorectal cancer: a meta-analysis. Clin Radiol 2005; 60 (09) 980-989
  • 422 Hartmann D et al. Colorectal polyps: detection with dark-lumen MR colonography versus conventional colonoscopy. Radiology 2006; 238 (01) 143-149
  • 423 Florie J et al. MR colonography with limited bowel preparation compared with optical colonoscopy in patients at increased risk for colorectal cancer. Radiology 2007; 243 (01) 122-131
  • 424 Morrin MM et al. Virtual colonoscopy: a kinder, gentler colorectal cancer screening test?. Lancet 1999; 354 (9184) 1048-1049
  • 425 Morrin MM et al. Role of virtual computed tomographic colonography in patients with colorectal cancers and obstructing colorectal lesions. Dis Colon Rectum 2000; 43 (03) 303-311
  • 426 Neri E et al. Colorectal cancer: role of CT colonography in preoperative evaluation after incomplete colonoscopy. Radiology 2002; 223 (03) 615-619
  • 427 Hartmann D et al. Incomplete conventional colonoscopy: magnetic resonance colonography in the evaluation of the proximal colon. Endoscopy 2005; 37 (09) 816-820
  • 428 Arora A, Singh P. Colonoscopy in patients 80 years of age and older is safe, with high success rate and diagnostic yield. Gastrointest Endosc 2004; 60 (03) 408-413
  • 429 Karajeh MA, Sanders DS, Hurlstone DP. Colonoscopy in elderly people is a safe procedure with a high diagnostic yield: a prospective comparative study of 2000 patients. Endoscopy 2006; 38 (03) 226-230
  • 430 Kiesslich R et al. Methylene blue-aided chromoendoscopy for the detection of intraepithelial neoplasia and colon cancer in ulcerative colitis. Gastroenterology 2003; 124 (04) 880-888
  • 431 Hurlstone DP et al. The role of high-magnification-chromoscopic colonoscopy in hereditary nonpolyposis colorectal cancer screening: a prospective “back-to-back” endoscopic study. Am J Gastroenterol 2005; 100 (10) 2167-2173
  • 432 Hurlstone DP et al. Indigo carmine-assisted high-magnification chromoscopic colonoscopy for the detection and characterisation of intraepithelial neoplasia in ulcerative colitis: a prospective evaluation. Endoscopy 2005; 37 (12) 1186-1192
  • 433 Lee JH et al. Detection of colorectal adenomas by routine chromoendoscopy with indigocarmine. Am J Gastroenterol 2003; 98 (06) 1284-1288
  • 434 Hurlstone DP et al. Detecting diminutive colorectal lesions at colonoscopy: a randomised controlled trial of pan-colonic versus targeted chromoscopy. Gut 2004; 53 (03) 376-380
  • 435 Trecca A et al. Advanced diagnostic tools: virtual colonoscopy and magnifying chromoendoscopy. Tech Coloproctol 2004; 8 (Suppl. 02) s279-s282
  • 436 Lapalus MG et al. Does chromoendoscopy with structure enhancement improve the colonoscopic adenoma detection rate?. Endoscopy 2006; 38 (05) 444-448
  • 437 Kudo S et al. Colonoscopic diagnosis and management of nonpolypoid early colorectal cancer. World J Surg 2000; 24 (09) 1081-1090
  • 438 Kiesslich R et al. Chromoendoscopy with indigocarmine improves the detection of adenomatous and nonadenomatous lesions in the colon. Endoscopy 2001; 33 (12) 1001-1006
  • 439 Kudo S et al. Pit pattern in colorectal neoplasia: endoscopic magnifying view. Endoscopy 2001; 33 (04) 367-373
  • 440 Brooker JC et al. Total colonic dye-spray increases the detection of diminutive adenomas during routine colonoscopy: a randomized controlled trial. Gastrointest Endosc 2002; 56 (03) 333-338
  • 441 Eisen GM et al. High-resolution chromoendoscopy for classifying colonic polyps: a multicenter study. Gastrointest Endosc 2002; 55 (06) 687-694
  • 442 Tsuda S et al. Flat and depressed colorectal tumours in a southern Swedish population: a prospective chromoendoscopic and histopathological study. Gut 2002; 51 (04) 550-555
  • 443 Bianco MA et al. Predictive value of magnification chromoendoscopy for diagnosing invasive neoplasia in nonpolypoid colorectal lesions and stratifying patients for endoscopic resection or surgery. Endoscopy 2006; 38 (05) 470-476
  • 444 Kato S et al. Magnifying colonoscopy as a non-biopsy technique for differential diagnosis of non-neoplastic and neoplastic lesions. World J Gastroenterol 2006; 12 (09) 1416-1420
  • 445 Hurlstone DP et al. Endoscopic morphological anticipation of submucosal invasion in flat and depressed colorectal lesions: clinical implications and subtype analysis of the kudo type V pit pattern using high-magnification-chromoscopic colonoscopy. Colorectal Dis 2004; 6 (05) 369-375
  • 446 Hurlstone DP et al. Efficacy of high magnification chromoscopic colonoscopy for the diagnosis of neoplasia in flat and depressed lesions of the colorectum: a prospective analysis. Gut 2004; 53 (02) 284-290
  • 447 Chiu HM et al. A prospective comparative study of narrow-band imaging, chromoendoscopy, and conventional colonoscopy in the diagnosis of colorectal neoplasia. Gut 2007; 56 (03) 373-379
  • 448 Dekker E et al. Narrow-band imaging compared with conventional colonoscopy for the detection of dysplasia in patients with longstanding ulcerative colitis. Endoscopy 2007; 39 (03) 216-221
  • 449 Su MY et al. Comparative study of conventional colonoscopy, chromoendoscopy, and narrow-band imaging systems in differential diagnosis of neoplastic and nonneoplastic colonic polyps. Am J Gastroenterol 2006; 101 (12) 2711-2716
  • 450 Kiesslich R et al. Confocal laser endoscopy for diagnosing intraepithelial neoplasias and colorectal cancer in vivo. Gastroenterology 2004; 127 (03) 706-713
  • 451 Nivatvongs S. Complications in colonoscopic polypectomy. An experience with 1,555 polypectomies. Dis Colon Rectum 1986; 29 (12) 825-830
  • 452 Reiertsen O et al. Complications of fiberoptic gastrointestinal endoscopy – five years’ experience in a central hospital. Endoscopy 1987; 19 (01) 1-6
  • 453 Waye JD, Lewis BS, Yessayan S. Colonoscopy: a prospective report of complications. J Clin Gastroenterol 1992; 15 (04) 347-351
  • 454 Waye JD, Kahn O, Auerbach ME. Complications of colonoscopy and flexible sigmoidoscopy. Gastrointest Endosc Clin N Am 1996; 6 (02) 343-377
  • 455 Hsieh YH et al. Is submucosal epinephrine injection necessary before polypectomy? A prospective, comparative study. Hepatogastroenterology 2001; 48 (41) 1379-1382
  • 456 Karita M, Cantero D, Okita K. Endoscopic diagnosis and resection treatment for flat adenoma with severe dysplasia. Am J Gastroenterol 1993; 88 (09) 1421-1423
  • 457 Kudo S et al. Endoscopic diagnosis and treatment of early colorectal cancer. World J Surg 1997; 21 (07) 694-701
  • 458 Heldwein W et al. The Munich Polypectomy Study (MUPS): prospective analysis of complications and risk factors in 4000 colonic snare polypectomies. Endoscopy 2005; 37 (11) 1116-1122
  • 459 Di Giorgio P et al. Detachable snare versus epinephrine injection in the prevention of postpolypectomy bleeding: a randomized and controlled study. Endoscopy 2004; 36 (10) 860-863
  • 460 Dobrowolski S et al. Prophylactic submucosal saline-adrenaline injection in colonoscopic polypectomy: prospective randomized study. Surg Endosc 2004; 18 (06) 990-993
  • 461 Katsinelos P et al. Endoloop-assisted polypectomy for large pedunculated colorectal polyps. Surg Endosc 2006; 20 (08) 1257-1261
  • 462 Paspatis GA et al. A prospective, randomized comparison of adrenaline injection in combination with detachable snare versus adrenaline injection alone in the prevention of postpolypectomy bleeding in large colonic polyps. Am J Gastroenterol 2006; 101 (12) 2805 ; quiz 2913
  • 463 Shioji K et al. Prophylactic clip application does not decrease delayed bleeding after colonoscopic polypectomy. Gastrointest Endosc 2003; 57 (06) 691-694
  • 464 Shiffman ML, Farrel MT, Yee YS. Risk of bleeding after endoscopic biopsy or polypectomy in patients taking aspirin or other NSAIDS. Gastrointest Endosc 1994; 40 (04) 458-462
  • 465 Hui AJ et al. Risk of colonoscopic polypectomy bleeding with anticoagulants and antiplatelet agents: analysis of 1657 cases. Gastrointest Endosc 2004; 59 (01) 44-48
  • 466 Yousfi M et al. Postpolypectomy lower gastrointestinal bleeding: potential role of aspirin. Am J Gastroenterol 2004; 99 (09) 1785-1789
  • 467 Ernst A et al. Effect of routine clopidogrel use on bleeding complications after transbronchial biopsy in humans. Chest 2006; 129 (03) 734-737
  • 468 Hurlstone DP et al. A prospective analysis of extended endoscopic mucosal resection for large rectal villous adenomas: an alternative technique to transanal endoscopic microsurgery. Colorectal Dis 2005; 7 (04) 339-344
  • 469 Gondal G et al. Biopsy of colorectal polyps is not adequate for grading of neoplasia. Endoscopy 2005; 37 (12) 1193-1197
  • 470 Waye JD et al. Small colon polyps. Am J Gastroenterol 1988; 83 (02) 120-122
  • 471 O’Brien MJ et al. The National Polyp Study. Patient and polyp characteristics associated with high-grade dysplasia in colorectal adenomas. Gastroenterology 1990; 98 (02) 371-379
  • 472 Nusko G et al. Risk of invasive carcinoma in colorectal adenomas assessed by size and site. Int J Colorectal Dis 1997; 12 (05) 267-271
  • 473 Bond JH. Clinical relevance of the small colorectal polyp. Endoscopy 2001; 33 (05) 454-457
  • 474 Arumugam PJ et al. Severe dysplastic lesions in the colon – how aggressive should we be?. Colorectal Dis 2002; 4 (05) 345-347
  • 475 Gschwantler M et al. High-grade dysplasia and invasive carcinoma in colorectal adenomas: a multivariate analysis of the impact of adenoma and patient characteristics. Eur J Gastroenterol Hepatol 2002; 14 (02) 183-188
  • 476 Burton S et al. Reliability of pre-operative biopsies in the histological grading of colorectal adenocarcinomas. Ann R Coll Surg Engl 2003; 85 (01) 23-25
  • 477 Hamilton SR, Aaltonen LA. Pathology and Genetics of Tumours of the Digestive System. World Health Organization Classification of Tumours. ed. Lyon: IARC Press; 2000
  • 478 Jass JR. Classification of colorectal cancer based on correlation of clinical, morphological and molecular features. Histopathology 2007; 50 (01) 113-130
  • 479 Makinen MJ. Colorectal serrated adenocarcinoma. Histopathology 2007; 50 (01) 131-150
  • 480 Deinlein P et al. Risk factors for lymphatic metastasis from pT1 colorectal adenocarcinoma. Pathologe 2003; 24 (05) 387-393
  • 481 Hermanek P. Polypectomy in the colorectum: histological and oncological aspects. Endoscopy 1983; 15: 158-161
  • 482 Kikuchi R et al. Management of early invasive colorectal cancer. Risk of recurrence and clinical guidelines. Dis Colon Rectum 1995; 38 (12) 1286-1295
  • 483 Okuyama T, Oya M, Ishikawa H. Budding as a risk factor for lymph node metastasis in pT1 or pT2 well-differentiated colorectal adenocarcinoma. Dis Colon Rectum 2002; 45 (05) 628-634
  • 484 Fruhmorgen P et al. Endoscopic Therapy of Early Colorectal Cancer (pT1) – A Prospective Study. Z Gastroenterol 2003; 41 (08) 703-710
  • 485 Frühmorgen P et al. Kolorektale Polypen. In: Empfehlungen der Deutschen Gesellschaft für Verdauungs- und Stoffwechselkrankheiten (DGVS) für die Durchführung endoskopischer Untersuchungen. 2000: 127-134
  • 486 Okabe S et al. Lymph node metastasis in T1 adenocarcinoma of the colon and rectum. J Gastrointest Surg 2004; 8 (08) 1032-1039 ; discussion 1039-1040
  • 487 Yamamoto S et al. The risk of lymph node metastasis in T1 colorectal carcinoma. Hepatogastroenterology 2004; 51 (58) 998-1000
  • 488 Hassan C et al. Histologic risk factors and clinical outcome in colorectal malignant polyp: a pooled-data analysis. Dis Colon Rectum 2005; 48 (08) 1588-1596
  • 489 Ueno H et al. Risk factors for an adverse outcome in early invasive colorectal carcinoma. Gastroenterology 2004; 127 (02) 385-394
  • 490 The Paris endoscopic classification of superficial neoplastic lesions: esophagus, stomach, and colon: November 30 to December 1 2002. Gastrointest Endosc 2003; 58 (Suppl. 06) S3-S43
  • 491 Nascimbeni R et al. Risk of lymph node metastasis in T1 carcinoma of the colon and rectum. Dis Colon Rectum 2002; 45 (02) 200-206
  • 492 Seitz U et al. Is endoscopic polypectomy an adequate therapy for malignant colorectal adenomas? Presentation of 114 patients and review of the literature. Dis Colon Rectum 2004; 47 (11) 1789-1796
  • 493 Provenzale D et al. Risk for colon adenomas in patients with rectosigmoid hyperplastic polyps. Ann Intern Med 1990; 113: 760-763
  • 494 Rex DK et al. Distal colonic hyperplastic polyps do not predict proximal adenomas in asymptomatic average-risk subjects. Gastroenterology 1992; 102: 317-319
  • 495 Sciallero S et al. Distal hyperplastic polyps do not predict proximal adenomas: results from a multicentric study of colorectal adenomas. Gastrointest Endosc 1997; 46 (02) 124-130
  • 496 Koide N et al. A case of hyperplastic polyposis of the colon with adenocarcinomas in hyperplastic polyps after long-term follow-up. Endoscopy 2002; 34 (06) 499-502
  • 497 Bressler B et al. Rates of new or missed colorectal cancers after colonoscopy and their risk factors: a population-based analysis. Gastroenterology 2007; 132 (01) 96-102
  • 498 Sawhney MS et al. Microsatellite instability in interval colon cancers. Gastroenterology 2006; 131 (06) 1700-1705
  • 499 Winawer SJ et al. Guidelines for colonoscopy surveillance after polypectomy: a consensus update by the US Multi-Society Task Force on Colorectal Cancer and the American Cancer Society. Gastroenterology 2006; 130 (06) 1872-1885
  • 500 Higaki S et al. Long-term follow-up of large flat colorectal tumors resected endoscopically. Endoscopy 2003; 35 (10) 845-849
  • 501 Regula J et al. Argon plasma coagulation after piecemeal polypectomy of sessile colorectal adenomas: long-term follow-up study. Endoscopy 2003; 35 (03) 212-218
  • 502 Seitz U et al. Long-term results of endoscopic removal of large colorectal adenomas. Endoscopy 2003; 35 (08) S41-S44
  • 503 Boix J et al. Endoscopic removal of large sessile colorectal adenomas: is it safe and effective?. Dig Dis Sci 2007; 52 (03) 840-844
  • 504 Baron JA et al. A randomized trial of aspirin to prevent colorectal adenomas. N Engl J Med 2003; 348 (10) 891-899
  • 505 Benamouzig R et al. Daily soluble aspirin and prevention of colorectal adenoma recurrence: one-year results of the APACC trial. Gastroenterology 2003; 125 (02) 328-336
  • 506 Imperiale TF. Aspirin and the prevention of colorectal cancer. N Engl J Med 2003; 348 (10) 879-880
  • 507 Bresalier RS et al. Cardiovascular events associated with rofecoxib in a colorectal adenoma chemoprevention trial. N Engl J Med 2005; 352 (11) 1092-1102
  • 508 Solomon SD et al. Cardiovascular risk associated with celecoxib in a clinical trial for colorectal adenoma prevention. N Engl J Med 2005; 352 (11) 1071-1080
  • 509 Psaty BM, Potter JD. Risks and benefits of celecoxib to prevent recurrent adenomas. N Engl J Med 2006; 355 (09) 950-952
  • 510 Weingarten MA, Zalmanovici A, Yaphe J. Dietary calcium supplementation for preventing colorectal cancer and adenomatous polyps. Cochrane Database Syst Rev 2005; 3: CD003548
  • 511 Fielding LP et al. Clinicopathological staging for colorectal cancer: an International Documentation System (IDS) and an International Comprehensive Anatomical Terminology (ICAT). J Gastroenterol Hepatol 1991; 6 (04) 325-344
  • 512 Soreide O et al. International standardization and documentation of the treatment of rectal cancer. In: Soreide O, Norstein J, , (eds) Rectal cancer surgery. Optimisation – standardization – documentation. Berlin Heidelberg New York.: Springer; 1997: 405-445
  • 513 UICC. TNM Classification of Malignant Tumours. Sobin LH, Wittekind C, (ed.) 6th ed. New York: John Wiley & Sons; 2002
  • 514 Adjuvant therapy for patients with colon and rectal cancer. Jama 1990; 264 (11) 1444-1450
  • 515 Nelson H et al. Guidelines 2000 for colon and rectal cancer surgery. J Natl Cancer Inst 2001; 93 (08) 583-596
  • 516 Pilipshen SJ et al. Patterns of pelvic recurrence following definitive resections of rectal cancer. Cancer 1984; 53 (06) 1354-1362
  • 517 Burton S et al. MRI directed multidisciplinary team preoperative treatment strategy: the way to eliminate positive circumferential margins?. Br J Cancer 2006; 94 (03) 351-357
  • 518 Segelman J et al. Differences in multidisciplinary team assessment and treatment between patients with stage IV colon and rectal cancer. Colorectal Dis 2009; 11 (07) 768-774
  • 519 MacDermid E et al. Improving patient survival with the colorectal cancer multi-disciplinary team. Colorectal Dis 2009; 11 (03) 291-295
  • 520 Barillari P et al. Effect of preoperative colonoscopy on the incidence of synchronous and metachronous neoplasms. Acta Chir Scand 1990; 156 (02) 163-166
  • 521 Faivre J. Endoscopic monitoring after excision of colorectal cancer. J Chir (Paris) 1997; 134 (07) 283-285
  • 522 Chen HS, Sheen-Chen SM. Synchronous and “early” metachronous colorectal adenocarcinoma: analysis of prognosis and current trends. Dis Colon Rectum 2000; 43 (08) 1093-1099
  • 523 Floriani I et al. Performance of imaging modalities in diagnosis of liver metastases from colorectal cancer: a systematic review and meta-analysis. J Magn Reson Imaging 2010; 31 (01) 19-31
  • 524 Rafaelsen SR, Jakobsen A. Contrast-enhanced ultrasound vs. multidetector-computed tomography for detecting liver metastases in colorectal cancer: a prospective, blinded, patient-by-patient analysis. Colorectal Dis 2011; 13 (04) 420-425
  • 525 Quaia E et al. Comparison of contrast-enhanced ultrasonography versus baseline ultrasound and contrast-enhanced computed tomography in metastatic disease of the liver: diagnostic performance and confidence. Eur Radiol 2006; 16 (07) 1599-1609
  • 526 Niekel MC, Bipat S, Stoker J. Diagnostic imaging of colorectal liver metastases with CT, MR imaging, FDG PET, and/or FDG PET/CT: a meta-analysis of prospective studies including patients who have not previously undergone treatment. Radiology 2010; 257 (03) 674-684
  • 527 Mainenti PP et al. Detection of colo-rectal liver metastases: prospective comparison of contrast enhanced US, multidetector CT, PET/CT, and 1.5 Tesla MR with extracellular and reticulo-endothelial cell specific contrast agents. Abdom Imaging 2010; 35 (05) 511-521
  • 528 McAndrew MR, Saba AK. Efficacy of routine preoperative computed tomography scans in colon cancer. Am Surg 1999; 65 (03) 205-208
  • 529 Barton JB et al. The utility of routine preoperative computed tomography scanning in the management of veterans with colon cancer. Am J Surg 2002; 183 (05) 499-503
  • 530 Dighe S et al. Diagnostic precision of CT in local staging of colon cancers: a meta-analysis. Clin Radiol 2010; 65 (09) 708-719
  • 531 Abdel-Nabi H et al. Staging of primary colorectal carcinomas with fluorine-18 fluorodeoxyglucose whole-body PET: correlation with histopathologic and CT findings. Radiology 1998; 206 (03) 755-760
  • 532 Akiyoshi T et al. Comparison of preoperative whole-body positron emission tomography with MDCT in patients with primary colorectal cancer. Colorectal Dis 2009; 11 (05) 464-469
  • 533 Furukawa H et al. Positron emission tomography scanning is not superior to whole body multidetector helical computed tomography in the preoperative staging of colorectal cancer. Gut 2006; 55 (07) 1007-1011
  • 534 Kam MH et al. Comparison of magnetic resonance imaging-fluorodeoxy-glucose positron emission tomography fusion with pathological staging in rectal cancer. Br J Surg 2010; 97 (02) 266-268
  • 535 Kinner S et al. Whole-body PET/CT-colonography: a possible new concept for colorectal cancer staging. Abdom Imaging 2007; 32 (05) 606-612
  • 536 Llamas-Elvira JM et al. Fluorine-18 fluorodeoxyglucose PET in the preoperative staging of colorectal cancer. Eur J Nucl Med Mol Imaging 2007; 34 (06) 859-867
  • 537 Ono K et al. Comparison of diffusion-weighted MRI and 2-[fluorine-18]-fluoro-2-deoxy-D-glucose positron emission tomography (FDG-PET) for detecting primary colorectal cancer and regional lymph node metastases. J Magn Reson Imaging 2009; 29 (02) 336-340
  • 538 Tateishi U et al. Non-enhanced CT versus contrast-enhanced CT in integrated PET/CT studies for nodal staging of rectal cancer. Eur J Nucl Med Mol Imaging 2007; 34 (10) 1627-1634
  • 539 Veit-Haibach P et al. Diagnostic accuracy of colorectal cancer staging with whole-body PET/CT colonography. JAMA 2006; 296 (21) 2590-2600
  • 540 Bassi MC et al. FDG-PET/CT imaging for staging and target volume delineation in preoperative conformal radiotherapy of rectal cancer. Int J Radiat Oncol Biol Phys 2008; 70 (05) 1423-1426
  • 541 Davey K et al. The impact of 18-fluorodeoxyglucose positron emission tomography-computed tomography on the staging and management of primary rectal cancer. Dis Colon Rectum 2008; 51 (07) 997-1003
  • 542 Gearhart SL et al. Improved staging with pretreatment positron emission tomography/computed tomography in low rectal cancer. Ann Surg Oncol 2006; 13 (03) 397-404
  • 543 Kantorova I et al. Routine (18)F-FDG PET preoperative staging of colorectal cancer: comparison with conventional staging and its impact on treatment decision making. J Nucl Med 2003; 44 (11) 1784-1788
  • 544 Nagata K et al. PET/CT colonography for the preoperative evaluation of the colon proximal to the obstructive colorectal cancer. Dis Colon Rectum 2008; 51 (06) 882-890
  • 545 Park IJ et al. Efficacy of PET/CT in the accurate evaluation of primary colorectal carcinoma. Eur J Surg Oncol 2006; 32 (09) 941-947
  • 546 Paskeviciute B et al. Impact of (18)F-FDG-PET/CT on staging and irradiation of patients with locally advanced rectal cancer. Strahlenther Onkol 2009; 185 (04) 260-265
  • 547 Ruers TJ et al. Improved selection of patients for hepatic surgery of colorectal liver metastases with (18)F-FDG PET: a randomized study. J Nucl Med 2009; 50 (07) 1036-1041
  • 548 Moulton CA. An Ontario Clinical Oncology Group (OCOG) randomized controlled trial (RCT) assessing FDG PET/CT in resectable liver colorectal adenocarcinoma metastases (CAM). J Clin Oncol 2011; abstr 3520
  • 549 Glazer ES et al. Effectiveness of positron emission tomography for predicting chemotherapy response in colorectal cancer liver metastases. Arch Surg 2010; 145 (04) 340-345 ; discussion 345
  • 550 Lubezky N et al. The role and limitations of 18-fluoro-2-deoxy-D-glucose positron emission tomography (FDG-PET) scan and computerized tomography (CT) in restaging patients with hepatic colorectal metastases following neoadjuvant chemotherapy: comparison with operative and pathological findings. J Gastrointest Surg 2007; 11 (04) 472-478
  • 551 Spatz J et al. Neoadjuvant chemotherapy affects staging of colorectal liver metastasis – a comparison of PET, CT and intraoperative ultrasound. Int J Colorectal Dis 2011; 26 (02) 165-171
  • 552 IQWIG. Positronenemissionstomographie (PET und PET/CT) bei rezidivierendem kolorektalen Karzinom – Vorbericht (vorläufige Nutzenbewertung). 2011
  • 553 Patel S et al. Positron emission tomography/computed tomographic scans compared to computed tomographic scans for detecting colorectal liver metastases: a systematic review. Ann Surg 2011; 253 (04) 666-671
  • 554 Taylor RA, Akhurst TJ, Yuman F. Evaluation with positron emission tomography before hepatic resection for metastatic colorectal cancer improves survival in patients with a high clinical risk score. 2007 Gastrointestinal Cancers Symposium, Abstract No: 240, 2007.
  • 555 Adie S et al. Resection of liver metastases from colorectal cancer: does preoperative chemotherapy affect the accuracy of PET in preoperative planning?. ANZ J Surg 2009; 79 (05) 358-361
  • 556 Levy M et al. Tumor markers in staging and prognosis of colorectal carcinoma. Neoplasma 2008; 55 (02) 138-1342
  • 557 Lewis MR et al. Metastatic colorectal adenocarcinoma involving the ovary with elevated serum CA125: a potential diagnostic pitfall. Gynecol Oncol 2007; 105 (02) 395-398
  • 558 Chen CC et al. Is it reasonable to add preoperative serum level of CEA and CA19-9 to staging for colorectal cancer?. J Surg Res 2005; 124 (02) 169-174
  • 559 Merkel S et al. The prognostic inhomogeneity in pT3 rectal carcinomas. Int J Colorectal Dis 2001; 16 (05) 298-304
  • 560 Nagtegaal ID, Quirke P. What is the role for the circumferential margin in the modern treatment of rectal cancer?. J Clin Oncol 2008; 26 (02) 303-312
  • 561 Bipat S et al. Rectal cancer: local staging and assessment of lymph node involvement with endoluminal US, CT, and MR imaging – a meta-analysis. Radiology 2004; 232 (03) 773-783
  • 562 Puli SR et al. Accuracy of endoscopic ultrasound to diagnose nodal invasion by rectal cancers: a meta-analysis and systematic review. Ann Surg Oncol 2009; 16 (05) 1255-1265
  • 563 Ahmetoglu A et al. MDCT with multiplanar reconstruction in the preoperative local staging of rectal tumor. Abdom Imaging 2011; 36 (01) 31-37
  • 564 Kim CK et al. Preoperative staging of rectal cancer: accuracy of 3-Tesla magnetic resonance imaging. Eur Radiol 2006; 16 (05) 972-980
  • 565 Kim YW et al. A prospective comparison study for predicting circumferential resection margin between preoperative MRI and whole mount sections in mid-rectal cancer: significance of different scan planes. Eur J Surg Oncol 2008; 34 (06) 648-654
  • 566 Kim YW et al. Factors related to preoperative assessment of the circumferential resection margin and the extent of mesorectal invasion by magnetic resonance imaging in rectal cancer: a prospective comparison study. World J Surg 2009; 33 (09) 1952-1960
  • 567 Matsuoka H et al. MRI diagnosis of mesorectal lymph node metastasis in patients with rectal carcinoma. what is the optimal criterion? Anticancer Res 2004; 24 (06) 4097-4101
  • 568 Wolberink SV et al. Multislice CT as a primary screening tool for the prediction of an involved mesorectal fascia and distant metastases in primary rectal cancer: a multicenter study. Dis Colon Rectum 2009; 52 (05) 928-934
  • 569 Purkayastha S et al. Magnetic resonance colonography vs. computed tomography colonography for the diagnosis of colorectal cancer: an indirect comparison. Colorectal Dis 2007; 9 (02) 100-111
  • 570 Torzilli G et al. Contrast-enhanced intraoperative ultrasonography during hepatectomies for colorectal cancer liver metastases. J Gastrointest Surg 2005; 9 (08) 1148-1153 ; discussion 1153-1154
  • 571 Zirngibl H, Husemann B, Hermanek P. Intraoperative spillage of tumor cells in surgery for rectal cancer. Dis Colon Rectum 1990; 33 (07) 610-614
  • 572 Cahill RA, Leroy J, Marescaux J. Could lymphatic mapping and sentinel node biopsy provide oncological providence for local resectional techniques for colon cancer? A review of the literature. BMC Surg 2008; 8: 17
  • 573 Wiese D et al. Ultrastaging of sentinel lymph nodes (SLNs) vs. non-SLNs in colorectal cancer – do we need both?. Am J Surg 2010; 199 (03) 354-358 ; discussion 358
  • 574 Goligher JC. Incidence and pathology of carcinoma of the colon and rectum. In: Surgery of the anus, rectum and colon. London: Balliére Tindall; 1984: 445
  • 575 Toyota S, Ohta H, Anazawa S. Rationale for extent of lymph node dissection for right colon cancer. Dis Colon Rectum 1995; 38 (07) 705-711
  • 576 Tan KY et al. Distribution of the first metastatic lymph node in colon cancer and its clinical significance. Colorectal Dis 2010; 12 (01) 44-47
  • 577 Lan YT et al. Significance of lymph node retrieval from the terminal ileum for patients with cecal and ascending colonic cancers. Ann Surg Oncol 2011; 18 (01) 146-152
  • 578 Chang GJ et al. Lymph node evaluation and survival after curative resection of colon cancer: systematic review. J Natl Cancer Inst 2007; 99 (06) 433-441
  • 579 Le VoyerTE et al. Colon cancer survival is associated with increasing number of lymph nodes analyzed: a secondary survey of intergroup trial INT-0089. J Clin Oncol 2003; 21 (15) 2912-2919
  • 580 Van Damme JP. Vascular anatomy in abdominal surgery. Stuttgart: Thieme; 1990
  • 581 Kanemitsu Y et al. Survival benefit of high ligation of the inferior mesenteric artery in sigmoid colon or rectal cancer surgery. Br J Surg 2006; 93 (05) 609-615
  • 582 Chin CC et al. Carcinoma obstruction of the proximal colon cancer and long-term prognosis – obstruction is a predictor of worse outcome in TNM stage II tumor. Int J Colorectal Dis 2010; 25 (07) 817-822
  • 583 Hohenberger W et al. Standardized surgery for colonic cancer: complete mesocolic excision and central ligation – technical notes and outcome. Colorectal Dis 2009; 11 (04) 354-364 ; discussion 364-365
  • 584 West NP et al. Multicentre experience with extralevator abdominoperineal excision for low rectal cancer. Br J Surg 2010; 97 (04) 588-599
  • 585 Bertelsen CA et al. Can the quality of colonic surgery be improved by standardization of surgical technique with complete mesocolic excision?. Colorectal Dis 2011; 13 (10) 1123-1129
  • 586 (NICE). N.I.f.C.E. Radiofrequency ablation for the treatment of colorectal metastases in the liver. London: 2011
  • 587 Kim KH et al. Comparative analysis of radiofrequency ablation and surgical resection for colorectal liver metastases. J Korean Surg Soc 2011; 81 (01) 25-34
  • 588 Mulier S et al. Radiofrequency ablation versus resection for resectable colorectal liver metastases: time for a randomized trial?. Ann Surg Oncol 2008; 15 (01) 144-157
  • 589 (NICE). N.I.f.C.E. Selective internal radiation therapy for colorectal metastases in the liver. London: 2011
  • 590 Townsend A, Price T, Karapetis C. Selective internal radiation therapy for liver metastases from colorectal cancer. Cochrane Database Syst Rev 2009; 4: CD007045
  • 591 Christophi C et al. Long-term survival of patients with unresectable colorectal liver metastases treated by percutaneous interstitial laser thermotherapy. World J Surg 2004; 28 (10) 987-994
  • 592 Wietzke-Braun P et al. Quality of life and outcome of ultrasound-guided laser interstitial thermo-therapy for non-resectable liver metastases of colorectal cancer. Eur J Gastroenterol Hepatol 2004; 16 (04) 389-395
  • 593 Abcarian H, Pearl RK. Simple technique for high ligation of the inferior mesenteric artery and vein. Dis Colon Rectum 1991; 34 (12) 1138
  • 594 Buunen M et al. Level of arterial ligation in total mesorectal excision (TME): an anatomical study. Int J Colorectal Dis 2009; 24 (11) 1317-1320
  • 595 Pezim ME, Nicholls RJ. Survival after high or low ligation of the inferior mesenteric artery during curative surgery for rectal cancer. Ann Surg 1984; 200 (06) 729-733
  • 596 Surtees P, Ritchie JK, Phillips RK. High versus low ligation of the inferior mesenteric artery in rectal cancer. Br J Surg 1990; 77 (06) 618-621
  • 597 Slanetz CA Jr, Grimson R. Effect of high and intermediate ligation on survival and recurrence rates following curative resection of colorectal cancer. Dis Colon Rectum 1997; 40 (10) 1205-1218 ; discussion 1218-1219
  • 598 Lange MM et al. Level of arterial ligation in rectal cancer surgery: low tie preferred over high tie. A review. Dis Colon Rectum 2008; 51 (07) 1139-1145
  • 599 Heald RJ, Husband EM, Ryall RD. The mesorectum in rectal cancer surgery – the clue to pelvic recurrence?. Br J Surg 1982; 69 (10) 613-616
  • 600 Bokey EL et al. Local recurrence after curative excision of the rectum for cancer without adjuvant therapy: role of total anatomical dissection. Br J Surg 1999; 86 (09) 1164-1170
  • 601 Hermanek PJ. Multiviszerale Resektion beim kolorektalen Karzinom. Erfahrungen der SGKRK-Studie. Langenbecks Arch Surg 1992; Kongressband: 95-100
  • 602 Havenga K et al. Male and female sexual and urinary function after total mesorectal excision with autonomic nerve preservation for carcinoma of the rectum. J Am Coll Surg 1996; 182 (06) 495-502
  • 603 Enker WE et al. Abdominoperineal resection via total mesorectal excision and autonomic nerve preservation for low rectal cancer. World J Surg 1997; 21 (07) 715-720
  • 604 Georgiou P et al. Extended lymphadenectomy versus conventional surgery for rectal cancer: a meta-analysis. Lancet Oncol 2009; 10 (11) 1053-1062
  • 605 Gohl J, Hohenberger W, Merkel S. Lymph node dissection in rectal carcinoma: TME and what else?. Onkologie 2009; 32 (01) 57-61
  • 606 Mortenson MM et al. Total mesorectal excision and pelvic node dissection for rectal cancer: an appraisal. Surg Oncol Clin N Am 2007; 16 (01) 177-197
  • 607 Koch M et al. Is the lateral lymph node compartment relevant?. Recent Results Cancer Res 2005; 165: 40-45
  • 608 Scott N et al. Total mesorectal excision and local recurrence: a study of tumour spread in the mesorectum distal to rectal cancer. Br J Surg 1995; 82 (08) 1031-1033
  • 609 Reynolds JV et al. Pathological evidence in support of total mesorectal excision in the management of rectal cancer. Br J Surg 1996; 83 (08) 1112-1115
  • 610 Hida J et al. Lymph node metastases detected in the mesorectum distal to carcinoma of the rectum by the clearing method: justification of total mesorectal excision. J Am Coll Surg 1997; 184 (06) 584-588
  • 611 Zaheer S et al. Surgical treatment of adenocarcinoma of the rectum. Ann Surg 1998; 227 (06) 800-811
  • 612 Leong AF. Selective total mesorectal excision for rectal cancer. Dis Colon Rectum 2000; 43 (09) 1237-1240
  • 613 Heald RJ, Karanjia ND. Results of radical surgery for rectal cancer. World J Surg 1992; 16 (05) 848-857
  • 614 Enker WE. Total mesorectal excision – the new golden standard of surgery for rectal cancer. Ann Med 1997; 29 (02) 127-133
  • 615 Lazorthes F et al. Distal intramural spread of carcinoma of the rectum correlated with lymph nodal involvement. Surg Gynecol Obstet 1990; 170 (01) 45-48
  • 616 Kwok SP et al. Prospective analysis of the distal margin of clearance in anterior resection for rectal carcinoma. Br J Surg 1996; 83 (07) 969-972
  • 617 Andreola S et al. Distal intramural spread in adenocarcinoma of the lower third of the rectum treated with total rectal resection and coloanal anastomosis. Dis Colon Rectum 1997; 40 (01) 25-29
  • 618 Goldstein NS, Soman A, Sacksner J. Disparate surgical margin lengths of colorectal resection specimens between in vivo and in vitro measurements. The effects of surgical resection and formalin fixation on organ shrinkage. Am J Clin Pathol 1999; 111 (03) 349-351
  • 619 Kiran RP, Lian L, Lavery IC. Does a subcentimeter distal resection margin adversely influence oncologic outcomes in patients with rectal cancer undergoing restorative proctectomy?. Dis Colon Rectum 2011; 54 (02) 157-163
  • 620 Rutkowski A et al. Distal bowel surgical margin shorter than 1 cm after preoperative radiation for rectal cancer: is it safe?. Ann Surg Oncol 2008; 15 (11) 3124-3131
  • 621 Brown CJ, Fenech DS, McLeod RS. Reconstructive techniques after rectal resection for rectal cancer. Cochrane Database Syst Rev 2008; 2: CD006040
  • 622 Fazio VW et al. A randomized multicenter trial to compare long-term functional outcome, quality of life, and complications of surgical procedures for low rectal cancers. Ann Surg 2007; 246 (03) 481-488 ; discussion 488-490
  • 623 Liao C et al. Meta-analysis of the colon J-pouch vs. transverse coloplasty pouch after anterior resection for rectal cancer. Colorectal Dis 2010; 12 (07) 624-631
  • 624 Siddiqui MR et al. A meta-analysis comparing side to end with colonic J-pouch formation after anterior resection for rectal cancer. Tech Coloproctol 2010; 14 (02) 113-123
  • 625 Hida J et al. Functional outcome after low anterior resection with low anastomosis for rectal cancer using the colonic J-pouch. Prospective randomized study for determination of optimum pouch size. Dis Colon Rectum 1996; 39 (09) 986-991
  • 626 Hohenberger W et al. Neoadjuvant radiochemotherapy for rectal cancer. Chirurg 2009; 80 (04) 294-302
  • 627 Artioukh DY. Controversial aspects of rectal cancer surgery following preoperative chemoradiation. Colorectal Dis 2010; 12 (Suppl. 02) 25-29
  • 628 Habr-Gama A et al. Operative versus nonoperative treatment for stage 0 distal rectal cancer following chemoradiation therapy: long-term results. Ann Surg 2004; 240 (04) 711-717 ; discussion 717-718
  • 629 Tekkis PP et al. Comparison of circumferential margin involvement between restorative and nonrestorative resections for rectal cancer. Colorectal Dis 2005; 7 (04) 369-374
  • 630 Nagtegaal ID et al. Low rectal cancer: a call for a change of approach in abdominoperineal resection. J Clin Oncol 2005; 23 (36) 9257-9264
  • 631 Nisar PJ, Scott HJ. Myocutaneous flap reconstruction of the pelvis after abdominoperineal excision. Colorectal Dis 2009; 11 (08) 806-816
  • 632 Montedori A et al. Covering ileo- or colostomy in anterior resection for rectal carcinoma. Cochrane Database Syst Rev 2010; 5: CD006878
  • 633 Lindgren R et al. What is the risk for a permanent stoma after low anterior resection of the rectum for cancer? A six-year follow-up of a multicenter trial. Dis Colon Rectum 2011; 54 (01) 41-47
  • 634 Klink CD et al. Protective ileostoma versus protective transverse stoma. What evidence is available?. Chirurg 2010; 81 (11) 974-977
  • 635 Rondelli F et al. Loop ileostomy versus loop colostomy for fecal diversion after colorectal or coloanal anastomosis: a meta-analysis. Int J Colorectal Dis 2009; 24 (05) 479-488
  • 636 Bass EM et al. Does preoperative stoma marking and education by the enterostomal therapist affect outcome?. Dis Colon Rectum 1997; 40 (04) 440-442
  • 637 Millan M et al. Preoperative stoma siting and education by stomatherapists of colorectal cancer patients: a descriptive study in twelve Spanish colorectal surgical units. Colorectal Dis 2010; 12 (07) e88-e92
  • 638 Chaudhri S et al. Preoperative intensive, community-based vs. traditional stoma education: a randomized, controlled trial. Dis Colon Rectum 2005; 48 (03) 504-509
  • 639 Hermanek P, Marzoli GP. Lokale Therapie des Rektumkarzinoms. Verfahren in kurativer Intention. Berlin Heidelberg Ney York Tokyo: Springer; 1994
  • 640 Winde G et al. Surgical cure for early rectal carcinomas (T1). Transanal endoscopic microsurgery vs. anterior resection. Dis Colon Rectum 1996; 39 (09) 969-976
  • 641 Sengupta S, Tjandra JJ. Local excision of rectal cancer: what is the evidence?. Dis Colon Rectum 2001; 44 (09) 1345-1361
  • 642 Matzel KE, Merkel S, Hohenberger W. Lokale Therapieprinzipien beim Rektumkarzinom. Chirurg 2003; 74 (10) 897-904
  • 643 Ptok H et al. Oncological outcome of local vs. radical resection of low-risk pT1 rectal cancer. Arch Surg 2007; 142 (07) 649-655 ; discussion 656
  • 644 You YN et al. Is the increasing rate of local excision for stage I rectal cancer in the United States justified? A nationwide cohort study from the National Cancer Database. Ann Surg 2007; 245 (05) 726-733
  • 645 Moore JS et al. Transanal endoscopic microsurgery is more effective than traditional transanal excision for resection of rectal masses. Dis Colon Rectum 2008; 51 (07) 1026-1030 ; discussion 1030-1031
  • 646 Sgourakis G et al. Transanal endoscopic microsurgery for T1 and T2 rectal cancers: a meta-analysis and meta-regression analysis of outcomes. Am Surg 2011; 77 (06) 761-772
  • 647 Bach SP et al. A predictive model for local recurrence after transanal endoscopic microsurgery for rectal cancer. Br J Surg 2009; 96 (03) 280-290
  • 648 Glimelius B, Pahlman L, Cervantes A. Rectal cancer: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up. Ann Oncol 2010; 21 (Suppl. 05) v82-v86
  • 649 Suppiah A et al. Transanal endoscopic microsurgery in early rectal cancer: time for a trial?. Colorectal Dis 2008; 10 (04) 314-327 ; discussion 327-329
  • 650 Valentini V et al. Multidisciplinary Rectal Cancer Management: 2nd European Rectal Cancer Consensus Conference (EURECA-CC2).  Radiother Oncol 2009; 92 (02) 148-163
  • 651 Hahnloser D et al. Immediate radical resection after local excision of rectal cancer: an oncologic compromise?. Dis Colon Rectum 2005; 48 (03) 429-437
  • 652 Schwenk W et al. Short term benefits for laparoscopic colorectal resection. Cochrane Database Syst Rev 2005; 3: CD003145
  • 653 Liang Y et al. Laparoscopic versus open colorectal resection for cancer: a meta-analysis of results of randomized controlled trials on recurrence. Eur J Surg Oncol 2008; 34 (11) 1217-1224
  • 654 Kuhry E et al. Long-term results of laparoscopic colorectal cancer resection. Cochrane Database Syst Rev 2008; 2: CD003432
  • 655 Guillou PJ et al. Short-term endpoints of conventional versus laparoscopic-assisted surgery in patients with colorectal cancer (MRC CLASICC trial): multicentre, randomised controlled trial. Lancet 2005; 365 (9472) 1718-1726
  • 656 Jayne DG et al. Five-year follow-up of the Medical Research Council CLASICC trial of laparoscopically assisted versus open surgery for colorectal cancer. Br J Surg 2010; 97 (11) 1638-1645
  • 657 Kwak JM et al. Robotic vs. laparoscopic resection of rectal cancer: short-term outcomes of a case-control study. Dis Colon Rectum 2011; 54 (02) 151-156
  • 658 Pigazzi A et al. Multicentric study on robotic tumor-specific mesorectal excision for the treatment of rectal cancer. Ann Surg Oncol 2010; 17 (06) 1614-1620
  • 659 Jacquet P, Sugarbaker PH. Clinical research methodologies in diagnosis and staging of patients with peritoneal carcinomatosis. Cancer Treat Res 1996; 82: 359-374
  • 660 Verwaal VJ et al. Randomized trial of cytoreduction and hyperthermic intraperitoneal chemotherapy versus systemic chemotherapy and palliative surgery in patients with peritoneal carcinomatosis of colorectal cancer. J Clin Oncol 2003; 21 (20) 3737-3743
  • 661 Verwaal VJ et al. 8-year follow-up of randomized trial: cytoreduction and hyperthermic intraperitoneal chemotherapy versus systemic chemotherapy in patients with peritoneal carcinomatosis of colorectal cancer. Ann Surg Oncol 2008; 15 (09) 2426-2432
  • 662 Cao C et al. A systematic review and meta-analysis of cytoreductive surgery with perioperative intraperitoneal chemotherapy for peritoneal carcinomatosis of colorectal origin. Ann Surg Oncol 2009; 16 (08) 2152-2165
  • 663 Khot UP et al. Systematic review of the efficacy and safety of colorectal stents. Br J Surg 2002; 89 (09) 1096-1102
  • 664 Stillwell AP, Buettner PG, Ho YH. Meta-analysis of survival of patients with stage IV colorectal cancer managed with surgical resection versus chemotherapy alone. World J Surg 2010; 34 (04) 797-807
  • 665 Poultsides GA et al. Outcome of primary tumor in patients with synchronous stage IV colorectal cancer receiving combination chemotherapy without surgery as initial treatment. J Clin Oncol 2009; 27 (20) 3379-3384
  • 666 Hermanek P, Guggenmoos-Holzmann I, Gall FP. Prognostic factors in rectal carcinoma. A contribution to the further development of tumor classification. Dis Colon Rectum 1989; 32 (07) 593-599
  • 667 Hermanek P, Hohenberger W. The importance of volume in colorectal cancer surgery. Eur J Surg Oncol 1996; 22 (03) 213-215
  • 668 Compton CC. Pathology report in colon cancer: what is prognostically important?. Dig Dis 1999; 17 (02) 67-79
  • 669 Wong JH et al. Number of nodes examined and staging accuracy in colorectal carcinoma. J Clin Oncol 1999; 17 (09) 2896-2900
  • 670 Compton C et al. American Joint Committee on Cancer Prognostic Factors Consensus Conference: Colorectal Working Group. Cancer 2000; 88 (07) 1739-1757
  • 671 Compton CC. Updated protocol for the examination of specimens from patients with carcinomas of the colon and rectum, excluding carcinoid tumors, lymphomas, sarcomas, and tumors of the vermiform appendix: a basis for checklists. Cancer Committee. Arch Pathol Lab Med 2000; 124 (07) 1016-1025
  • 672 Hermanek P. Methodik der histopathologischen Untersuchung von Resektionen kolorektaler Karzinome. Chir Gastroenterol 2000; 16: 255-259
  • 673 Hermanek P. Lymph nodes and malignant tumors. Zentralbl Chir 2000; 125 (10) 790-795
  • 674 Junginger THP, Klimpfinger M. Klassifikation maligner Tumoren des Gastrointestinaltraktes I. Berlin Heidelberg New York: Springer Verlag; 2002
  • 675 Wittekind C et al. TNM residual tumor classification revisited. Cancer 2002; 94 (09) 2511-2516
  • 676 Leibl S, Tsybrovskyy O, Denk H. How many lymph nodes are necessary to stage early and advanced adenocarcinoma of the sigmoid colon and upper rectum?. Virchows Arch 2003; 443 (02) 133-138
  • 677 Sobin LH. TNM, sixth edition: new developments in general concepts and rules. Semin Surg Oncol 2003; 21 (01) 19-22
  • 678 Dworak O, Keilholz L, Hoffmann A. Pathological features of rectal cancer after preoperative radiochemotherapy. Int J Colorectal Dis 1997; 12 (01) 19-23
  • 679 Wright CM et al. Prognostic significance of extensive microsatellite instability in sporadic clinicopathological stage C colorectal cancer. Br J Surg 2000; 87 (09) 1197-1202
  • 680 Popat S, Hubner R, Houlston RS. Systematic review of microsatellite instability and colorectal cancer prognosis. J Clin Oncol 2005; 23 (03) 609-618
  • 681 Benatti P et al. Microsatellite instability and colorectal cancer prognosis. Clin Cancer Res 2005; 11 (23) 8332-8340
  • 682 Malesci A et al. Reduced likelihood of metastases in patients with microsatellite-unstable colorectal cancer. Clin Cancer Res 2007; 13 (13) 3831-3839
  • 683 Leopoldo S et al. Two subtypes of mucinous adenocarcinoma of the colorectum: clinicopathological and genetic features. Ann Surg Oncol 2008; 15 (05) 1429-1439
  • 684 Lanza G et al. Medullary-type poorly differentiated adenocarcinoma of the large bowel: a distinct clinicopathologic entity characterized by microsatellite instability and improved survival. J Clin Oncol 1999; 17 (08) 2429-2438
  • 685 Parc Y et al. Prognostic significance of microsatellite instability determined by immunohistochemical staining of MSH2 and MLH1 in sporadic T3N0M0 colon cancer. Gut 2004; 53 (03) 371-375
  • 686 Gafa R et al. Sporadic colorectal adenocarcinomas with high-frequency microsatellite instability. Cancer 2000; 89 (10) 2025-2037
  • 687 Lanza G et al. Immunohistochemical pattern of MLH1 / MSH2 expression is related to clinical and pathological features in colorectal adenocarcinomas with microsatellite instability. Mod Pathol 2002; 15 (07) 741-749
  • 688 Lindor NM et al. Immunohistochemistry versus microsatellite instability testing in phenotyping colorectal tumors. J Clin Oncol 2002; 20 (04) 1043-1048
  • 689 Overbeek LI et al. Interpretation of immunohistochemistry for mismatch repair proteins is only reliable in a specialized setting. Am J Surg Pathol 2008; 32 (08) 1246-1251
  • 690 Prandi M et al. Prognostic evaluation of stage B colon cancer patients is improved by an adequate lymphadenectomy: results of a secondary analysis of a large scale adjuvant trial. Ann Surg 2002; 235 (04) 458-463
  • 691 Ogino S et al. Negative lymph node count is associated with survival of colorectal cancer patients, independent of tumoral molecular alterations and lymphocytic reaction. Am J Gastroenterol 2010; 105 (02) 420-433
  • 692 Swanson RS et al. The prognosis of T3N0 colon cancer is dependent on the number of lymph nodes examined. Ann Surg Oncol 2003; 10 (01) 65-71
  • 693 Carloss H et al. The impact of number of lymph nodes removed on five-year survival in stage II colon and rectal cancer. J Ky Med Assoc 2004; 102 (08) 345-347
  • 694 Fazio L et al. Association between colonic screening, subject characteristics, and stage of colorectal cancer. Am J Gastroenterol 2005; 100 (11) 2531-2539
  • 695 Wong SL et al. Hospital lymph node examination rates and survival after resection for colon cancer. JAMA 2007; 298 (18) 2149-2154
  • 696 Qiu HB et al. Ratio of metastatic to resected lymph nodes enhances to predict survival in patients with stage III colorectal cancer. Ann Surg Oncol 2011; 18 (06) 1568-1574
  • 697 Wang J et al. Should total number of lymph nodes be used as a quality of care measure for stage III colon cancer?. Ann Surg 2009; 249 (04) 559-563
  • 698 Chen SL et al. Lymph node ratio as a quality and prognostic indicator in stage III colon cancer. Ann Surg 2011; 253 (01) 82-87
  • 699 Ha YH et al. Influence of preoperative chemoradiotherapy on the number of lymph nodes retrieved in rectal cancer. Ann Surg 2010; 252 (02) 336-340
  • 700 West NP et al. Complete mesocolic excision with central vascular ligation produces an oncologically superior specimen compared with standard surgery for carcinoma of the colon. J Clin Oncol 2010; 28 (02) 272-278
  • 701 West NP et al. Pathology grading of colon cancer surgical resection and its association with survival: a retrospective observational study. Lancet Oncol 2008; 9 (09) 857-865
  • 702 Quirke P et al. Effect of the plane of surgery achieved on local recurrence in patients with operable rectal cancer: a prospective study using data from the MRC CR07 and NCIC-CTG CO16 randomised clinical trial. Lancet 2009; 373 (9666) 821-828
  • 703 Tilney HS et al. The influence of circumferential resection margins on long-term outcomes following rectal cancer surgery. Dis Colon Rectum 2009; 52 (10) 1723-1729
  • 704 Bernstein TE et al. Circumferential resection margin as a prognostic factor in rectal cancer. Br J Surg 2009; 96 (11) 1348-1357
  • 705 West NP et al. Evidence of the oncologic superiority of cylindrical abdominoperineal excision for low rectal cancer. J Clin Oncol 2008; 26 (21) 3517-3522
  • 706 Leite JS et al. Clinical significance of macroscopic completeness of mesorectal resection in rectal cancer. Colorectal Dis 2011; 13 (04) 381-386
  • 707 Kreienberg R et al. Interdisziplinäre S3-Leitlinie für die Diagnostik, Therapie und Nachsorge des Mammakarzinoms. Informationszentrum für Standards in der Onkologie (ISTO), Deutsche Krebsgesellschaft e.V. 2008; 1. Aktualisierung
  • 708 Edwards AG, Hailey S, Maxwell M. Psychological interventions for women with metastatic breast cancer. Cochrane Database Syst Rev 2004; 2: CD004253
  • 709 Sheard T, Maguire P. The effect of psychological interventions on anxiety and depression in cancer patients: results of two meta-analyses. Br J Cancer 1999; 80 (11) 1770-1780
  • 710 Keller M et al. Recognition of distress and psychiatric morbidity in cancer patients: a multi-method approach. Ann Oncol 2004; 15 (08) 1243-1249
  • 711 Sharpe M et al. Major depression in outpatients attending a regional cancer centre: screening and unmet treatment needs. Br J Cancer 2004; 90 (02) 314-320
  • 712 Singer S, Das-Munshi J, Brahler E. Prevalence of mental health conditions in cancer patients in acute care – a meta-analysis. Ann Oncol 2010; 21 (05) 925-930
  • 713 Zabora J et al. The prevalence of psychological distress by cancer site. Psychooncology 2001; 10 (01) 19-28
  • 714 Jansen L et al. Health-related quality of life during the 10 years after diagnosis of colorectal cancer: a population-based study. J Clin Oncol 2011; 29 (24) 3263-3269
  • 715 Lynch BM et al. Describing and predicting psychological distress after colorectal cancer. Cancer 2008; 112 (06) 1363-1370
  • 716 Miovic M, Block S. Psychiatric disorders in advanced cancer. Cancer 2007; 110 (08) 1665-1676
  • 717 Ramsey SD et al. Quality of life in survivors of colorectal carcinoma. Cancer 2000; 88 (06) 1294-1303
  • 718 Zettl S, Hartlapp J (eds.) Sexualstörungen durch Krankheit und Therapie. Heidelberg: ed. Springer; 1997: S. 59
  • 719 Fallowfield L et al. Psychiatric morbidity and its recognition by doctors in patients with cancer. Br J Cancer 2001; 84 (08) 1011-1015
  • 720 Sollner W et al. How successful are oncologists in identifying patient distress, perceived social support, and need for psychosocial counselling?. Br J Cancer 2001; 84 (02) 179-185
  • 721 Ell K et al. Randomized controlled trial of collaborative care management of depression among low-income patients with cancer. J Clin Oncol 2008; 26 (27) 4488-4496
  • 722 Strong V et al. Management of depression for people with cancer (SMaRT oncology 1): a randomised trial. Lancet 2008; 372 (9632) 40-48
  • 723 Herschbach P, Weis J (eds.) Screeningverfahren in der Psychoonkologie. Berlin: Deutsche Krebsgesellschaft; 2008
  • 724 NHMRC. Clinical practice guidelines for the psychosocial care of adults with cancer. 2003; 1-237
  • 725 Turner J et al. Clinical practice guidelines for the psychosocial care of adults with cancer. Psychooncology 2005; 14 (03) 159-173
  • 726 Weis J et al. Psychoonkologie: Konzepte und Aufgaben einer jungen Fachdisziplin. Onkologe 2007; 13 (02) 185-194
  • 727 Edwards AG, Hulbert-Williams N, Neal RD. Psychological interventions for women with metastatic breast cancer. Cochrane Database Syst Rev 2008; 3: CD004253
  • 728 Faller H et al. Effects of psychooncological interventions on emotional distress and quality of life in adult cancer patients: systematic review and meta-analysis. Nat J Cancer in press.
  • 729 Goedendorp MM et al. Psychosocial interventions for reducing fatigue during cancer treatment in adults. Cochrane Database Syst Rev 2009; 1: CD006953
  • 730 Jacobsen PB, Jim HS. Psychosocial interventions for anxiety and depression in adult cancer patients: achievements and challenges. CA Cancer J Clin 2008; 58 (04) 214-230
  • 731 Luebbert K, Dahme B, Hasenbring M. The effectiveness of relaxation training in reducing treatment-related symptoms and improving emotional adjustment in acute non-surgical cancer treatment: a meta-analytical review. Psychooncology 2001; 10 (06) 490-502
  • 732 Osborn RL, Demoncada AC, Feuerstein M. Psychosocial interventions for depression, anxiety, and quality of life in cancer survivors: meta-analyses. Int J Psychiatry Med 2006; 36 (01) 13-34
  • 733 Rehse B, Pukrop R. Effects of psychosocial interventions on quality of life in adult cancer patients: meta analysis of 37 published controlled outcome studies. Patient Educ Couns 2003; 50 (02) 179-186
  • 734 Uitterhoeve RJ et al. Psychosocial interventions for patients with advanced cancer – a systematic review of the literature. Br J Cancer 2004; 91 (06) 1050-1062
  • 735 Williams S, Dale J. The effectiveness of treatment for depression/depressive symptoms in adults with cancer: a systematic review. Br J Cancer 2006; 94 (03) 372-390
  • 736 Iwashyna TJ, Lamont EB. Effectiveness of adjuvant fluorouracil in clinical practice: a population-based cohort study of elderly patients with stage III colon cancer. J Clin Oncol 2002; 20 (19) 3992-3998
  • 737 Lonardi S, Stefani M, Jirillo A et al. Benefit of fluorouracil and folinic acid adjuvant in colon cancer. Journal of Clinical Oncology 2006; ASCO Annual Meeting Proceedings (Post-Meeting Edition) 24 (Suppl. 18) Abstract 13564
  • 738 Sargent DJ et al. A pooled analysis of adjuvant chemotherapy for resected colon cancer in elderly patients. N Engl J Med 2001; 345 (15) 1091-1097
  • 739 Popescu RA et al. Adjuvant or palliative chemotherapy for colorectal cancer in patients 70 years or older. J Clin Oncol 1999; 17 (08) 2412-2418
  • 740 Goldberg RM, Tabah-Fisch I, Bleiberg H et al. Pooled Analysis of Safety and Efficacy of Oxaliplatin Plus Fluorouracil/Leucovorin Administered Bimonthly in Elderly Patients With Colorectal Cancer. Journal of Clinical Oncology 2006; 24 (25) 4085-4091
  • 741 Fata F et al. Efficacy and toxicity of adjuvant chemotherapy in elderly patients with colon carcinoma: a 10-year experience of the Geisinger Medical Center. Cancer 2002; 94 (07) 1931-1938
  • 742 Francini G et al. Folinic acid and 5-fluorouracil as adjuvant chemotherapy in colon cancer. Gastroenterology 1994; 106 (04) 899-906
  • 743 O’Connell MJ et al. Controlled trial of fluorouracil and low-dose leucovorin given for 6 months as postoperative adjuvant therapy for colon cancer. J Clin Oncol 1997; 15 (01) 246-250
  • 744 Dube S, Heyen F, Jenicek M. Adjuvant chemotherapy in colorectal carcinoma: results of a meta-analysis. Dis Colon Rectum 1997; 40 (01) 35-41
  • 745 Gill S et al. Pooled analysis of fluorouracil-based adjuvant therapy for stage II and III colon cancer: who benefits and by how much?. J Clin Oncol 2004; 22 (10) 1797-1806
  • 746 Efficacy of adjuvant fluorouracil and folinic acid in colon cancer. International Multicentre Pooled Analysis of Colon Cancer Trials (IMPACT) investigators. Lancet 1995; 345 (8955) 939-944
  • 747 Figueredo A et al. Adjuvant therapy for stage II colon cancer after complete resection. Provincial Gastrointestinal Disease Site Group. Cancer Prev Control 1997; 1 (05) 379-392
  • 748 Efficacy of adjuvant fluorouracil and folinic acid in B2 colon cancer. International Multicentre Pooled Analysis of B2 Colon Cancer Trials (IMPACT B2) Investigators. J Clin Oncol 1999; 17 (05) 1356-1363
  • 749 Mamounas E et al. Comparative efficacy of adjuvant chemotherapy in patients with Dukes’ B versus Dukes’ C colon cancer: results from four National Surgical Adjuvant Breast and Bowel Project adjuvant studies (C-01, C-02, C-03, and C-04). J Clin Oncol 1999; 17 (05) 1349-1355
  • 750 Benson 3rd AB et al. American Society of Clinical Oncology recommendations on adjuvant chemotherapy for stage II colon cancer. J Clin Oncol 2004; 22 (16) 3408-3419
  • 751 Quasar Collaborative G et al. Adjuvant chemotherapy versus observation in patients with colorectal cancer: a randomised study. Lancet 2007; 370 (9604) 2020-2029
  • 752 Gramont A, Boni C, Navarro M et al. Oxaliplatin/5FU/LV in adjuvant colon cancer: Updated efficacy results of the MOSAIC trial, including survival, with a median follow-up of six years. Journal of Clinical Oncology 2007; ASCO Annual Meeting Proceedings (Post-Meeting Edition) 25 (Suppl. 18) Abstract 4007
  • 753 Moertel CG et al. Intergroup study of fluorouracil plus levamisole as adjuvant therapy for stage II/Dukes’ B2 colon cancer. J Clin Oncol 1995; 13 (12) 2936-2943
  • 754 Taal BG, Van Tinteren H, Zoetmulder FA. Adjuvant 5FU plus levamisole in colonic or rectal cancer: improved survival in stage II and III. Br J Cancer 2001; 85 (10) 1437-1443
  • 755 Schrag D et al. Adjuvant chemotherapy use for Medicare beneficiaries with stage II colon cancer. J Clin Oncol 2002; 20 (19) 3999-4005
  • 756 Merkel S et al. High-risk groups of patients with Stage II colon carcinoma. Cancer 2001; 92 (06) 1435-1443
  • 757 Petersen VC et al. Identification of objective pathological prognostic determinants and models of prognosis in Dukes’ B colon cancer. Gut 2002; 51 (01) 65-69
  • 758 Morris M et al. Population-based study of prognostic factors in stage II colonic cancer. Br J Surg 2006; 93 (07) 866-871
  • 759 Burdy G et al. Identifying patients with T3-T4 node-negative colon cancer at high risk of recurrence. Dis Colon Rectum 2001; 44 (11) 1682-1688
  • 760 Jestin P et al. Emergency surgery for colonic cancer in a defined population. Br J Surg 2005; 92 (01) 94-100
  • 761 McArdle CS, McMillan DC, Hole DJ. The impact of blood loss, obstruction and perforation on survival in patients undergoing curative resection for colon cancer. Br J Surg 2006; 93 (04) 483-488
  • 762 Caplin S et al. For patients with Dukes’ B (TNM Stage II) colorectal carcinoma, examination of six or fewer lymph nodes is related to poor prognosis. Cancer 1998; 83 (04) 666-672
  • 763 George S et al. Will Rogers revisited: prospective observational study of survival of 3592 patients with colorectal cancer according to number of nodes examined by pathologists. Br J Cancer 2006; 95 (07) 841-847
  • 764 Chen SL, Bilchik AJ. More extensive nodal dissection improves survival for stages I to III of colon cancer: a population-based study. Ann Surg 2006; 244 (04) 602-610
  • 765 Moertel CG et al. Levamisole and fluorouracil for adjuvant therapy of resected colon carcinoma. N Engl J Med 1990; 322 (06) 352-358
  • 766 Hermanek P, Hutter RV, Sobin LH. Prognostic grouping: the next step in tumor classification. J Cancer Res Clin Oncol 1990; 116 (05) 513-516
  • 767 Martinez-Lopez E et al. Allelic loss on chromosome 18q as a prognostic marker in stage II colorectal cancer. Gastroenterology 1998; 114 (06) 1180-1187
  • 768 Ogunbiyi OA et al. Confirmation that chromosome 18q allelic loss in colon cancer is a prognostic indicator. J Clin Oncol 1998; 16 (02) 427-433
  • 769 Jernvall P et al. Loss of heterozygosity at 18q21 is indicative of recurrence and therefore poor prognosis in a subset of colorectal cancers. Br J Cancer 1999; 79 (05) 903-908
  • 770 Font A et al. Prognostic value of K-ras mutations and allelic imbalance on chromosome 18q in patients with resected colorectal cancer. Dis Colon Rectum 2001; 44 (04) 549-557
  • 771 Diep CB et al. Genetic tumor markers with prognostic impact in Dukes’ stages B and C colorectal cancer patients. J Clin Oncol 2003; 21 (05) 820-829
  • 772 Carethers JM et al. Prognostic significance of allelic lost at chromosome 18q21 for stage II colorectal cancer. Gastroenterology 1998; 114 (06) 1188-1195
  • 773 Lanza G et al. Immunohistochemical test for MLH1 and MSH2 expression predicts clinical outcome in stage II and III colorectal cancer patients. J Clin Oncol 2006; 24 (15) 2359-2367
  • 774 Sinicrope FA et al. Prognostic impact of microsatellite instability and DNA ploidy in human colon carcinoma patients. Gastroenterology 2006; 131 (03) 729-737
  • 775 Araujo SE et al. DNA ploidy status and prognosis in colorectal cancer: a meta-analysis of published data. Dis Colon Rectum 2007; 50 (11) 1800-1810
  • 776 Ribic CM et al. Tumor microsatellite-instability status as a predictor of benefit from fluorouracil-based adjuvant chemotherapy for colon cancer. N Engl J Med 2003; 349 (03) 247-257
  • 777 Elsaleh H, Iacopetta B. Microsatellite instability is a predictive marker for survival benefit from adjuvant chemotherapy in a population-based series of stage III colorectal carcinoma. Clin Colorectal Cancer 2001; 1 (02) 104-109
  • 778 Andre T et al. Oxaliplatin, fluorouracil, and leucovorin as adjuvant treatment for colon cancer. N Engl J Med 2004; 350 (23) 2343-2351
  • 779 Kuebler JP et al. Oxaliplatin combined with weekly bolus fluorouracil and leucovorin as surgical adjuvant chemotherapy for stage II and III colon cancer: results from NSABP C-07. J Clin Oncol 2007; 25 (16) 2198-2204
  • 780 Schmoll HJ et al. Phase III trial of capecitabine plus oxaliplatin as adjuvant therapy for stage III colon cancer: a planned safety analysis in 1,864 patients. J Clin Oncol 2007; 25 (01) 102-109
  • 781 Van Cutsem E, Labianca R, Hossfeld D et al. PETACC 3, Randomized phase III trial comparing infused irinotecan/5-fluorouracil (5-FU)/folinic acid (IF) versus 5-FU/FA (F) in stage III colon cancer patients (pts). (PETACC 3). Journal of Clinical Oncology 2005; ASCO Annual Meeting Proceedings Abstract LBA8
  • 782 Ychou M, Raoul J, Douillard J et al. , for the GI Group of the FNCLCC and the FFCD A phase III randomized trial of LV5FU2+CPT-11 vs. LV5FU2 alone in adjuvant high risk colon cancer (FNCLCC Accord02 / FFCD9802). Journal of Clinical Oncology 2005; ASCO Annual Meeting Proceedings 2005 23: Abstract 3502 (Suppl 16, Part I of II):
  • 783 Saltz LB et al. Irinotecan fluorouracil plus leucovorin is not superior to fluorouracil plus leucovorin alone as adjuvant treatment for stage III colon cancer: results of CALGB 89803. J Clin Oncol 2007; 25 (23) 3456-3461
  • 784 Twelves C et al. Capecitabine as adjuvant treatment for stage III colon cancer. N Engl J Med 2005; 352 (26) 2696-2704
  • 785 Lembersky BC et al. Oral uracil and tegafur plus leucovorin compared with intravenous fluorouracil and leucovorin in stage II and III carcinoma of the colon: results from National Surgical Adjuvant Breast and Bowel Project Protocol C-06. J Clin Oncol 2006; 24 (13) 2059-2064
  • 786 Sakamoto J et al. Efficacy of oral adjuvant therapy after resection of colorectal cancer: 5-year results from three randomized trials. J Clin Oncol 2004; 22 (03) 484-492
  • 787 Carrato A, Köhne C, Bedenne L et al. for AIO/CAO, FFCD, TTD, EORTC olinic acid modulated bolus 5-FU or infusional 5-FU for adjuvant treatment of patients of UICC stage III colon cancer: Preliminary analysis of the PETACC-2-study. F. Journal of Clinical Oncology 2006; ASCO Annual Meeting Proceedings (Post-Meeting Edition) 2006; 24 (Suppl 18): Abstract 3563
  • 788 Andre T, Quinaux E, Louvet C et al. GERCOR. Updated results at 6 year of the GERCOR C96.1 phase III study comparing LV5FU2 to monthly 5FU-leucovorin (mFufol) as adjuvant treatment for Dukes B2 and C colon cancer patients. Journal of Clinical Oncology 2005; . ASCO Annual Meeting Proceedings. 2005 23 (Suppl 16): Abstract 3522
  • 789 Andre T et al. Semimonthly versus monthly regimen of fluorouracil and leucovorin administered for 24 or 36 weeks as adjuvant therapy in stage II and III colon cancer: results of a randomized trial. J Clin Oncol 2003; 21 (15) 2896-2903
  • 790 Arkenau HT, Rettig K, Porschen R. Adjuvant chemotherapy in curative resected colon carcinoma: 5-fluorouracil/leucovorin versus high-dose 5-fluorouracil 24-h infusion/leucovorin versus high-dose 5-fluorouracil 24-h infusion. Int J Colorectal Dis 2005; 20 (03) 258-261
  • 791 Chau I et al. A randomised comparison between 6 months of bolus fluorouracil/leucovorin and 12 weeks of protracted venous infusion fluorouracil as adjuvant treatment in colorectal cancer. Ann Oncol 2005; 16 (04) 549-557
  • 792 Poplin EA et al. Phase III Southwest Oncology Group 9415/Intergroup 0153 randomized trial of fluorouracil, leucovorin, and levamisole versus fluorouracil continuous infusion and levamisole for adjuvant treatment of stage III and high-risk stage II colon cancer. J Clin Oncol 2005; 23 (09) (Suppl. 05) 1819-1825
  • 793 O’Connell MJ et al. Prospectively randomized trial of postoperative adjuvant chemotherapy in patients with high-risk colon cancer. J Clin Oncol 1998; 16 (01) 295-300
  • 794 Haller DG et al. Phase III study of fluorouracil, leucovorin, and levamisole in high-risk stage II and III colon cancer: final report of Intergroup 0089. J Clin Oncol 2005; 23 (34) 8671-8678
  • 795 Kapiteijn E et al. Preoperative radiotherapy combined with total mesorectal excision for resectable rectal cancer. N Engl J Med 2001; 345 (09) 638-646
  • 796 Rodel C, Sauer R. Neoadjuvant radiotherapy and radiochemotherapy for rectal cancer. Recent Results Cancer Res 2005; 165: 221-230
  • 797 Peeters KC et al. The TME trial after a median follow-up of 6 years: increased local control but no survival benefit in irradiated patients with resectable rectal carcinoma. Ann Surg 2007; 246 (05) 693-701
  • 798 Folkesson J et al. Swedish Rectal Cancer Trial: long lasting benefits from radiotherapy on survival and local recurrence rate. J Clin Oncol 2005; 23 (24) 5644-5650
  • 799 Baxter NN, Garcia-Aguilar J. Organ preservation for rectal cancer. J Clin Oncol 2007; 25 (08) 1014-1020
  • 800 Rengan R et al. Distal cT2N0 rectal cancer: is there an alternative to abdominoperineal resection?. J Clin Oncol 2005; 23 (22) 4905-4912
  • 801 Colorectal Cancer Collaborative Group. Adjuvant radiotherapy for rectal cancer: a systematic overview of 8,507 patients from 22 randomised trials. Lancet 2001; 358 (9290) 1291-1304
  • 802 Camma C et al. Preoperative radiotherapy for resectable rectal cancer: A meta-analysis. Jama 2000; 284 (08) 1008-1015
  • 803 Frykholm GJ, Glimelius B, Pahlman L. Preoperative or postoperative irradiation in adenocarcinoma of the rectum: final treatment results of a randomized trial and an evaluation of late secondary effects. Dis Colon Rectum 1993; 36 (06) 564-572
  • 804 Sauer R et al. Preoperative versus postoperative chemoradiotherapy for rectal cancer. N Engl J Med 2004; 351 (17) 1731-1740
  • 805 Marijnen CA et al. Impact of short-term preoperative radiotherapy on health-related quality of life and sexual functioning in primary rectal cancer: report of a multicenter randomized trial. J Clin Oncol 2005; 23 (09) 1847-1858
  • 806 Peeters KC et al. Late side effects of short-course preoperative radiotherapy combined with total mesorectal excision for rectal cancer: increased bowel dysfunction in irradiated patients – a Dutch colorectal cancer group study. J Clin Oncol 2005; 23 (25) 6199-6206
  • 807 Junginger T et al. Rectal carcinoma: is too much neoadjuvant therapy performed? Proposals for a more selective MRI based indication. Zentralbl Chir 2006; 131 (04) 275-284
  • 808 Smith N, Brown G. Preoperative staging of rectal cancer. Acta Oncol 2008; 47: 20-31
  • 809 Sebag-Montefiore D, Stephens R, Quirke P et al. for the NCRI colorectal cancer study group and CRO 7 participants Routine short course pre-op radiotherapy or selective post-op chemoradiotherapy for resectable rectal cancer? Preliminary results of the MRC CR07 randomised trial. Journal of Clinical Oncology 2006; ASCO Annual Meeting Proceedings (Post-Meeting Edition) 2006 24 (Suppl. 18) Abstract 3511
  • 810 Bujko K et al. Sphincter preservation following preoperative radiotherapy for rectal cancer: report of a randomised trial comparing short-term radiotherapy vs. conventionally fractionated radiochemotherapy. Radiother Oncol 2004; 72 (01) 15-24
  • 811 Bujko K et al. Long-term results of a randomized trial comparing preoperative short-course radiotherapy with preoperative conventionally fractionated chemoradiation for rectal cancer. Br J Surg 2006; 93 (10) 1215-1223
  • 812 Marijnen CA et al. No downstaging after short-term preoperative radiotherapy in rectal cancer patients. J Clin Oncol 2001; 19 (07) 1976-1984
  • 813 Bosset JF et al. Chemotherapy with preoperative radiotherapy in rectal cancer. N Engl J Med 2006; 355 (11) 1114-1123
  • 814 Gerard JP et al. Preoperative radiotherapy with or without concurrent fluorouracil and leucovorin in T3-4 rectal cancers: results of FFCD 9203. J Clin Oncol 2006; 24 (28) 4620-4625
  • 815 Rodel C, Sauer R. Integration of novel agents into combined-modality treatment for rectal cancer patients. Strahlenther Onkol 2007; 183 (05) 227-235
  • 816 Prolongation of the disease-free interval in surgically treated rectal carcinoma. N Engl J Med 1985; 312 (23) 1465-1472
  • 817 Krook JE et al. Effective surgical adjuvant therapy for high-risk rectal carcinoma. N Engl J Med 1991; 324 (11) 709-715
  • 818 Merkel S, Mannsmann U, Siassi M et al. The prognostic inhomogeneity in pT3 rectal carcinomas. Int J Colorectal Dis 2001; 16: 298-304
  • 819 Gunderson LL, Sargent DJ, Tepper JE et al. Impact of T and N substage on survival and disease relapse in adjuvant rectal cancer: a pooled analysis. Int J Radiat Oncol Biol Phys 2002; 54: 386-96
  • 820 Marijnen CA et al. Radiotherapy does not compensate for positive resection margins in rectal cancer patients: report of a multicenter randomized trial. Int J Radiat Oncol Biol Phys 2003; 55 (05) 1311-1320
  • 821 O’Connell MJ et al. Improving adjuvant therapy for rectal cancer by combining protracted-infusion fluorouracil with radiation therapy after curative surgery. N Engl J Med 1994; 331: 502-507
  • 822 Smalley SR et al. Phase III trial of fluorouracil-based chemotherapy regimens plus radiotherapy in postoperative adjuvant rectal cancer: GI INT 0144. J Clin Oncol 2006; 24 (22) 3542-3547
  • 823 Tepper JE et al. Adjuvant therapy in rectal cancer: analysis of stage, sex, and local control – final report of intergroup 0114. J Clin Oncol 2002; 20 (07) 1744-1750
  • 824 Lee JH et al. Randomized trial of postoperative adjuvant therapy in stage II and III rectal cancer to define the optimal sequence of chemotherapy and radiotherapy: a preliminary report. J Clin Oncol 2002; 20 (07) 1751-1758
  • 825 Kim BITK, Lee J, Lee J et al. Randomized trial of postoperative adjuvant therapy in stage II and III rectal cancer to define the optimal sequence of chemotherapy and radiotherapy: A final report. ASCO Meeting Abstracts 2007; 25: 4050
  • 826 Rodel C, Sauer R. Radiotherapy and concurrent radiochemotherapy for rectal cancer. Surg Oncol 2004; 13 (02) 93-101
  • 827 Akasu T et al. Adjuvant chemotherapy with uracil-tegafur for pathological stage III rectal cancer after mesorectal excision with selective lateral pelvic lymphadenectomy: a multicenter randomized controlled trial. Jpn J Clin Oncol 2006; 36 (04) 237-244
  • 828 Collette L, Bosset J, den Dulk M et al. Patients with curative resection of cT3-4 rectal cancer after preoperative radiotherapy or radiochemotherapy: does anybody benefit from adjuvant fluorouracil-based chemotherapy? A trial of the European Organisation for Research and Treatment of Cancer Radiation Oncology Group. J Clin Oncol 2007; 25: 4379-4386
  • 829 Lehnert T, Knaebel H, Duck M et al. Sequential hepatic and pulmonary resections for metastatic colorectal cancer. Br J Surg 1999; 86: 241-243
  • 830 Saito Y et al. Pulmonary metastasectomy for 165 patients with colorectal carcinoma: A prognostic assessment. J Thorac Cardiovasc Surg 2002; 124 (05) 1007-1013
  • 831 Pfannschmidt J et al. Prognostic factors and survival after complete resection of pulmonary metastases from colorectal carcinoma: experiences in 167 patients. J Thorac Cardiovasc Surg 2003; 126 (03) 732-739
  • 832 Lee WS et al. Pulmonary resection for metastases from colorectal cancer: prognostic factors and survival. Int J Colorectal Dis 2007; 22 (06) 699-704
  • 833 Pfannschmidt J, Dienemann H, Hoffmann H. Surgical resection of pulmonary metastases from colorectal cancer: a systematic review of published series. Ann Thorac Surg 2007; 84 (01) 324-338
  • 834 Poston GJ et al. OncoSurge: a strategy for improving resectability with curative intent in metastatic colorectal cancer. J Clin Oncol 2005; 23 (28) 7125-7134
  • 835 Nordlinger B et al. Surgical resection of colorectal carcinoma metastases to the liver. A prognostic scoring system to improve case selection, based on 1568 patients. Association Francaise de Chirurgie. Cancer 1996; 77 (07) 1254-1262
  • 836 Fong Y et al. Liver resection for colorectal metastases. J Clin Oncol 1997; 15 (03) 938-946
  • 837 Scheele J et al. Resection of colorectal liver metastases. What prognostic factors determine patient selection?. Chirurg 2001; 72 (05) 547-560
  • 838 Kato T et al. Therapeutic results for hepatic metastasis of colorectal cancer with special reference to effectiveness of hepatectomy: analysis of prognostic factors for 763 cases recorded at 18 institutions. Dis Colon Rectum 2003; 46 (Suppl. 10) S22-S31
  • 839 Fong Y, Fortner J, Sun RL et al. Clinical score for predicting recurrence after hepatic resection for metastatic colorectal cancer: analysis of 1001 consecutive cases. Ann Surg 1999; 230 (03) 309-318 ; discussion 318-321
  • 840 Schmiegel W et al. Update S3-guideline “colorectal cancer” 2008. Z Gastroenterol 2008; 46 (08) 799-840
  • 841 Nordlinger B et al. Perioperative chemotherapy with FOLFOX4 and surgery versus surgery alone for resectable liver metastases from colorectal cancer (EORTC Intergroup trial 40983): a randomised controlled trial. Lancet 2008; 371 (9617) 1007-1016
  • 842 Leonard GD, Brenner B, Kemeny NE. Neoadjuvant chemotherapy before liver resection for patients with unresectable liver metastases from colorectal carcinoma. J Clin Oncol 2005; 23 (09) 2038-2048
  • 843 Lorenz M et al. Prospective pilot study of neoadjuvant chemotherapy with 5-fluorouracil, folinic acid and oxaliplatin in resectable liver metastases of colorectal cancer. Analysis of 42 neoadjuvant chemotherapies. Zentralbl Chir 2003; 128 (02) 87-94
  • 844 Wein A et al. Neoadjuvant treatment with weekly high-dose 5-Fluorouracil as 24-hour infusion, folinic acid and oxaliplatin in patients with primary resectable liver metastases of colorectal cancer. Oncology 2003; 64 (02) 131-138
  • 845 Gruenberger B et al. Bevacizumab, capecitabine, and oxaliplatin as neoadjuvant therapy for patients with potentially curable metastatic colorectal cancer. J Clin Oncol 2008; 26 (11) 1830-1835
  • 846 Langer B, Bleiberg H, Labianca R et al. Fluorouracil (FU) plus l-leucovorin (l-LV) versus observation after potentially curative resection of liver or lung metastases from colorectal cancer (CRC): results of the ENG (EORTC/NCIC CTG/GIVIO) randomized trial. Proc Am Soc Clin Oncol 2002; 21 (abstr 592)
  • 847 Mitry E, Fields A, Bleiberg H et al. Adjuvant chemotherapy after potentially curative resection of metastases from colorectal cancer. A meta-analysis of two randomized trials. Journal of Clinical Oncology 2006; ASCO Annual Meeting Proceedings Part I 2006; 24 (Suppl. 18) Abstract 3524
  • 848 Portier G et al. Multicenter randomized trial of adjuvant fluorouracil and folinic acid compared with surgery alone after resection of colorectal liver metastases: FFCD ACHBTH AURC 9002 trial. J Clin Oncol 2006; 24 (31) 4976-4982
  • 849 Parks R et al. Adjuvant chemotherapy improves survival after resection of hepatic colorectal metastases: analysis of data from two continents. J Am Coll Surg 2007; 204 (05) 753-761 ; discussion 761-763
  • 850 Figueras J et al. Resection rate and effect of postoperative chemotherapy on survival after surgery for colorectal liver metastases. Br J Surg 2001; 88 (07) 980-985
  • 851 Scheithauer W et al. Randomised comparison of combination chemotherapy plus supportive care with supportive care alone in patients with metastatic colorectal cancer. Bmj 1993; 306 (6880) 752-755
  • 852 Nordic Gastrointestinal Tumor Adjuvant Therapy Group. Expectancy or primary chemotherapy in patients with advanced asymptomatic colorectal cancer: a randomized trial. J Clin Oncol 1992; 10 (06) 904-911
  • 853 Mattioli R et al. High activity and reduced neurotoxicity of bi-fractionated oxaliplatin plus 5-fluorouracil/leucovorin for elderly patients with advanced colorectal cancer. Ann Oncol 2005; 16 (07) 1147-1151
  • 854 Feliu J et al. XELOX (capecitabine plus oxaliplatin) as first-line treatment for elderly patients over 70 years of age with advanced colorectal cancer. Br J Cancer 2006; 94 (07) 969-975
  • 855 Sastre J et al. Irinotecan in combination with fluorouracil in a 48-hour continuous infusion as first-line chemotherapy for elderly patients with metastatic colorectal cancer: a Spanish Cooperative Group for the Treatment of Digestive Tumors study. J Clin Oncol 2005; 23 (15) 3545-3551
  • 856 Barrueco J, Marshall J, Mitchell E et al. Safety and efficacy of first-line irinotecan/fluoropymidine combinations in mCRC patients >65 years compared with those <65: The BICC-C study. Journal of Clinical Oncology 2007; ASCO Annual Meeting Proceedings Part I 2007; 25 (Suppl. 18) Abstract 4076
  • 857 Folprecht G, Seymour MT, Saltz L et al. Irinotecan/Fluorouracil Combination in First-Line Therapy of Older and Younger Patients With Metastatic Colorectal Cancer: Combined Analysis of 2,691 Patients in Randomized Controlled Trials. Journal of Clinical Oncology 2008; 26 (09) 1443-1451
  • 858 Giacchetti S et al. Long-term survival of patients with unresectable colorectal cancer liver metastases following infusional chemotherapy with 5-fluorouracil, leucovorin, oxaliplatin and surgery. Ann Oncol 1999; 10 (06) 663-669
  • 859 Falcone A et al. Phase III trial of infusional fluorouracil, leucovorin, oxaliplatin, and irinotecan (FOLFOXIRI) compared with infusional fluorouracil, leucovorin, and irinotecan (FOLFIRI) as first-line treatment for metastatic colorectal cancer: the Gruppo Oncologico Nord Ovest. J Clin Oncol 2007; 25 (13) 1670-1676
  • 860 Van Cutsem E, Nowacki M, Lang I et al. Randomized phase III study of irinotecan and 5-FU/FA with or without cetuximab in the first-line treatment of patients with metastatic colorectal cancer (mCRC): The CRYSTAL trial. Journal of Clinical Oncology 2007; . ASCO Annual Meeting Proceedings Part I 2007 25 (Suppl. 18) Abstract 4000
  • 861 Van Cutsem E, Lang I, D’haens G et al. KRAS status and efficacy in the first-line treatment of patients with metastatic colorectal cancer (mCRC) treated with FOLFIRI with or without cetuximab: The CRYSTAL experience. J Clin Oncol 2008; 26 (abstr 2)
  • 862 Folprecht G et al. Neoadjuvant treatment of unresectable colorectal liver metastases: correlation between tumour response and resection rates. Ann Oncol 2005; 16 (08) 1311-1319
  • 863 Souglakos J et al. FOLFOXIRI (folinic acid, 5-fluorouracil, oxaliplatin and irinotecan) vs. FOLFIRI (folinic acid, 5-fluorouracil and irinotecan) as first-line treatment in metastatic colorectal cancer (MCC): a multicentre randomised phase III trial from the Hellenic Oncology Research Group (HORG). Br J Cancer 2006; 94 (06) 798-805
  • 864 Saltz LB et al. Bevacizumab in combination with oxaliplatin-based chemotherapy as first-line therapy in metastatic colorectal cancer: a randomized phase III study. J Clin Oncol 2008; 26 (12) 2013-2019
  • 865 Aloia T et al. Liver histology and surgical outcomes after preoperative chemotherapy with fluorouracil plus oxaliplatin in colorectal cancer liver metastases. J Clin Oncol 2006; 24 (31) 4983-4990
  • 866 Vauthey JN et al. Chemotherapy regimen predicts steatohepatitis and an increase in 90-day mortality after surgery for hepatic colorectal metastases. J Clin Oncol 2006; 24 (13) 2065-2072
  • 867 Benoist S et al. Complete response of colorectal liver metastases after chemotherapy: does it mean cure?. J Clin Oncol 2006; 24 (24) 3939-3945
  • 868 Koopman M et al. Sequential versus combination chemotherapy with capecitabine, irinotecan, and oxaliplatin in advanced colorectal cancer (CAIRO): a phase III randomised controlled trial. Lancet 2007; 370 (9582) 135-142
  • 869 Schmoll HJ, Sargent D. Single agent fluorouracil for first-line treatment of advanced colorectal cancer as standard?. Lancet 2007; 370 (9582) 105-107
  • 870 Seymour MT et al. Different strategies of sequential and combination chemotherapy for patients with poor prognosis advanced colorectal cancer (MRC FOCUS): a randomised controlled trial. Lancet 2007; 370 (9582) 143-152
  • 871 Dy GK et al. Impact of complete response to chemotherapy on overall survival in advanced colorectal cancer: results from Intergroup N9741. J Clin Oncol 2007; 25 (23) 3469-3474
  • 872 Grothey A et al. Survival of patients with advanced colorectal cancer improves with the availability of fluorouracil-leucovorin, irinotecan, and oxaliplatin in the course of treatment. J Clin Oncol 2004; 22 (07) 1209-1214
  • 873 Petrelli N et al. The modulation of fluorouracil with leucovorin in metastatic colorectal carcinoma: a prospective randomized phase III trial. Gastrointestinal Tumor Study Group. J Clin Oncol 1989; 7 (10) 1419-1426
  • 874 Poon MA et al. Biochemical modulation of fluorouracil: evidence of significant improvement of survival and quality of life in patients with advanced colorectal carcinoma. J Clin Oncol 1989; 7 (10) 1407-18
  • 875 Lokich JJ et al. A prospective randomized comparison of continuous infusion fluorouracil with a conventional bolus schedule in metastatic colorectal carcinoma: a Mid-Atlantic Oncology Program Study. J Clin Oncol 1989; 7 (04) 425-432
  • 876 Gramont A et al. Randomized trial comparing monthly low-dose leucovorin and fluorouracil bolus with bimonthly high-dose leucovorin and fluorouracil bolus plus continuous infusion for advanced colorectal cancer: a French intergroup study. J Clin Oncol 1997; 15 (02) 808-815
  • 877 Efficacy of intravenous continuous infusion of fluorouracil compared with bolus administration in advanced colorectal cancer. J Clin Oncol 1998; 16 (01) 301-308
  • 878 Clarke DE, Raffin TA. Infectious complications of indwelling long-term central venous catheters. Chest 1990; 97 (04) 966-972
  • 879 Prandoni P et al. Treatment of deep venous thrombosis by fixed doses of a low-molecular-weight heparin (CY216). Haemostasis 1990; 20 (Suppl. 01) 220-223
  • 880 Verso M, Agnelli G. Venous thromboembolism associated with long-term use of central venous catheters in cancer patients. J Clin Oncol 2003; 21 (19) 3665-3675
  • 881 Liu G et al. Patient preferences for oral versus intravenous palliative chemotherapy. J Clin Oncol 1997; 15 (01) 110-115
  • 882 Borner MM et al. Patient preference and pharmacokinetics of oral modulated UFT versus intravenous fluorouracil and leucovorin: a randomised crossover trial in advanced colorectal cancer. Eur J Cancer 2002; 38 (03) 349-358
  • 883 Twelves C et al. A randomised cross-over trial comparing patient preference for oral capecitabine and 5-fluorouracil/leucovorin regimens in patients with advanced colorectal cancer. Ann Oncol 2006; 17 (02) 239-245
  • 884 Van Cutsem E et al. Oral capecitabine compared with intravenous fluorouracil plus leucovorin in patients with metastatic colorectal cancer: results of a large phase III study. J Clin Oncol 2001; 19 (21) 4097-4106
  • 885 Hoff PM et al. Comparison of oral capecitabine versus intravenous fluorouracil plus leucovorin as first-line treatment in 605 patients with metastatic colorectal cancer: results of a randomized phase III study. J Clin Oncol 2001; 19 (08) 2282-2292
  • 886 Van Cutsem E et al. Oral capecitabine vs. intravenous 5-fluorouracil and leucovorin: integrated efficacy data and novel analyses from two large, randomised, phase III trials. Br J Cancer 2004; 90 (06) 1190-1197
  • 887 Kohne CH et al. Clinical determinants of survival in patients with 5-fluorouracil-based treatment for metastatic colorectal cancer: results of a multivariate analysis of 3825 patients. Ann Oncol 2002; 13 (02) 308-317
  • 888 Gramont A et al. Leucovorin and fluorouracil with or without oxaliplatin as first-line treatment in advanced colorectal cancer. J Clin Oncol 2000; 18 (16) 2938-2947
  • 889 Giacchetti S et al. Phase III trial comparing 4-day chronomodulated therapy versus 2-day conventional delivery of fluorouracil, leucovorin, and oxaliplatin as first-line chemotherapy of metastatic colorectal cancer: the European Organisation for Research and Treatment of Cancer Chronotherapy Group. J Clin Oncol 2006; 24 (22) 3562-3569
  • 890 Giacchetti S et al. Phase III multicenter randomized trial of oxaliplatin added to chronomodulated fluorouracil-leucovorin as first-line treatment of metastatic colorectal cancer. J Clin Oncol 2000; 18 (01) 136-147
  • 891 Douillard JY et al. Irinotecan combined with fluorouracil compared with fluorouracil alone as first-line treatment for metastatic colorectal cancer: a multicentre randomised trial. Lancet 2000; 355 (9209) 1041-1047
  • 892 Kohne CH et al. Phase III study of weekly high-dose infusional fluorouracil plus folinic acid with or without irinotecan in patients with metastatic colorectal cancer: European Organisation for Research and Treatment of Cancer Gastrointestinal Group Study 40986. J Clin Oncol 2005; 23 (22) 4856-4865
  • 893 Saltz LB et al. Irinotecan plus fluorouracil and leucovorin for metastatic colorectal cancer. Irinotecan Study Group. N Engl J Med 2000; 343 (13) 905-914
  • 894 Tournigand C et al. FOLFIRI followed by FOLFOX6 or the reverse sequence in advanced colorectal cancer: a randomized GERCOR study. J Clin Oncol 2004; 22 (02) 229-237
  • 895 Colucci G et al. Phase III randomized trial of FOLFIRI versus FOLFOX4 in the treatment of advanced colorectal cancer: a multicenter study of the Gruppo Oncologico Dell’Italia Meridionale. J Clin Oncol 2005; 23 (22) 4866-4875
  • 896 Goldberg RM et al. A randomized controlled trial of fluorouracil plus leucovorin, irinotecan, and oxaliplatin combinations in patients with previously untreated metastatic colorectal cancer. J Clin Oncol 2004; 22 (01) 23-30
  • 897 Goldberg RM et al. Randomized controlled trial of reduced-dose bolus fluorouracil plus leucovorin and irinotecan or infused fluorouracil plus leucovorin and oxaliplatin in patients with previously untreated metastatic colorectal cancer: a North American Intergroup Trial. J Clin Oncol 2006; 24 (21) 3347-3353
  • 898 Comella P et al. Oxaliplatin plus high-dose folinic acid and 5-fluorouracil i. v. bolus (OXAFAFU) versus irinotecan plus high-dose folinic acid and 5-fluorouracil i. v. bolus (IRIFAFU) in patients with metastatic colorectal carcinoma: a Southern Italy Cooperative Oncology Group phase III trial. Ann Oncol 2005; 16 (06) 878-886
  • 899 Diaz-Rubio E et al. Phase III study of capecitabine plus oxaliplatin compared with continuous-infusion fluorouracil plus oxaliplatin as first-line therapy in metastatic colorectal cancer: final report of the Spanish Cooperative Group for the Treatment of Digestive Tumors Trial. J Clin Oncol 2007; 25 (27) 4224-4230
  • 900 Porschen R et al. Phase III study of capecitabine plus oxaliplatin compared with fluorouracil and leucovorin plus oxaliplatin in metastatic colorectal cancer: a final report of the AIO Colorectal Study Group. J Clin Oncol 2007; 25 (27) 4217-4223
  • 901 Cassidy J et al. Randomized phase III study of capecitabine plus oxaliplatin compared with fluorouracil/folinic acid plus oxaliplatin as first-line therapy for metastatic colorectal cancer. J Clin Oncol 2008; 26 (12) 2006-2012
  • 902 Fuchs CS et al. Randomized, controlled trial of irinotecan plus infusional, bolus, or oral fluoropyrimidines in first-line treatment of metastatic colorectal cancer: results from the BICC-C Study. J Clin Oncol 2007; 25 (30) 4779-4786
  • 903 Kohne CH et al. Irinotecan combined with infusional 5-fluorouracil/folinic acid or capecitabine plus celecoxib or placebo in the first-line treatment of patients with metastatic colorectal cancer. EORTC study 40015. Ann Oncol 2008; 19 (05) 920-926
  • 904 Schmiegel WH, Reinacher-Schick A, Freier W et al. Comparable safety and response rate with bevacizumab in combination with capecitabine/oxaliplatin (CapOx/Bev) versus capecitabine/irinotecan (CapIri/Bev) in advanced CRC (mCRC): A randomized phase II study of the AIO GI tumor study group. Journal of Clinical Oncology 2007; ASCO Annual Meeting Proceedings Part I 2007 25 (Suppl. 18) 4034
  • 905 Kabbinavar FF et al. Addition of bevacizumab to bolus fluorouracil and leucovorin in first-line metastatic colorectal cancer: results of a randomized phase II trial. J Clin Oncol 2005; 23 (16) 3697-3705
  • 906 Hurwitz H et al. Bevacizumab plus irinotecan, fluorouracil, and leucovorin for metastatic colorectal cancer. N Engl J Med 2004; 350 (23) 2335-2342
  • 907 Bokemeyer C, Bondarenko I, Makhson A et al. Cetuximab plus 5-FU/FA/oxaliplatin (FOLFOX-4) versus FOLFOX-4 in the first-line treatment of metastatic colorectal cancer (mCRC): OPUS, a randomized phase II study. Journal of Clinical Oncology 2007; ASCO Annual Meeting Proceedings Part I 2007 25 (Suppl. 18) 4035
  • 908 Folprecht G et al. Cetuximab and irinotecan/5-fluorouracil/folinic acid is a safe combination for the first-line treatment of patients with epidermal growth factor receptor expressing metastatic colorectal carcinoma. Ann Oncol 2006; 17 (03) 450-456
  • 909 Tournigand C et al. OPTIMOX1: a randomized study of FOLFOX4 or FOLFOX7 with oxaliplatin in a stop-and-Go fashion in advanced colorectal cancer – a GERCOR study. J Clin Oncol 2006; 24 (03) 394-400
  • 910 Maindrault-Goebel F, Lledo G, Chibaudel B et al. Final results of OPTIMOX2, a large randomized phase II study of maintenance therapy or chemotherapy-free intervals (CFI) after FOLFOX in patients with metastatic colorectal cancer (MRC): A GERCOR study. Journal of Clinical Oncology 2007; ASCO Annual Meeting Proceedings Part I 2007 25 (Suppl. 18) 4013
  • 911 Maughan TS et al. Comparison of intermittent and continuous palliative chemotherapy for advanced colorectal cancer: a multicentre randomised trial. Lancet 2003; 361 (9356) 457-464
  • 912 Labianca R et al. Alternating versus continuous “FOLFIRI” in advanced colorectal cancer (ACC): A randomized “GISCAD” trial. Journal of Clinical Oncology 2006; ASCO Annual Meeting Proceedings Part I 2006; 24 (Suppl 18)
  • 913 Cunningham D et al. Randomised trial of irinotecan plus supportive care versus supportive care alone after fluorouracil failure for patients with metastatic colorectal cancer. Lancet 1998; 352 (9138) 1413-1418
  • 914 Rougier P et al. Randomised trial of irinotecan versus fluorouracil by continuous infusion after fluorouracil failure in patients with metastatic colorectal cancer. Lancet 1998; 352 (9138) 1407-1412
  • 915 Rothenberg ML et al. Superiority of oxaliplatin and fluorouracil-leucovorin compared with either therapy alone in patients with progressive colorectal cancer after irinotecan and fluorouracil-leucovorin: interim results of a phase III trial. J Clin Oncol 2003; 21 (11) 2059-2069
  • 916 Cunningham D et al. Cetuximab monotherapy and cetuximab plus irinotecan in irinotecan-refractory metastatic colorectal cancer. N Engl J Med 2004; 351 (04) 337-345
  • 917 Sobrero AF et al. EPIC: phase III trial of cetuximab plus irinotecan after fluoropyrimidine and oxaliplatin failure in patients with metastatic colorectal cancer. J Clin Oncol 2008; 26 (14) 2311-2319
  • 918 Giantonio BJ et al. Bevacizumab in combination with oxaliplatin, fluorouracil, and leucovorin (FOLFOX4) for previously treated metastatic colorectal cancer: results from the Eastern Cooperative Oncology Group Study E3200. J Clin Oncol 2007; 25 (12) 1539-1544
  • 919 Rothenberg ML et al. Phase III trial of capecitabine + oxaliplatin (XELOX) vs. 5-fluorouracil (5-FU), leucovorin (LV), and oxaliplatin (FOLFOX4) as 2nd-line treatment for patients with metastatic colorectal cancer (MCRC). Journal of Clinical Oncology 2007; ASCO Annual Meeting Proceedings (Post-Meeting Edition) 2007 25 (Suppl. 18)
  • 920 Eng C, Maurel J, Scheithauer W et al. Impact on quality of life of adding cetuximab to irinotecan in patients who have failed prior oxaliplatin-based therapy: the EPIC trial. Proc Am Soc Clin Oncol 2007; 25: 164s Abstract 4003
  • 921 Rao S et al. Phase II study of capecitabine and mitomycin C as first-line treatment in patients with advanced colorectal cancer. Br J Cancer 2004; 91 (05) 839-843
  • 922 Chong G et al. Capecitabine and mitomycin C as third-line therapy for patients with metastatic colorectal cancer resistant to fluorouracil and irinotecan. Br J Cancer 2005; 93 (05) 510-514
  • 923 Lim DH et al. Mitomycin-C and capecitabine as third-line chemotherapy in patients with advanced colorectal cancer: a phase II study. Cancer Chemother Pharmacol 2005; 56 (01) 10-14
  • 924 Alliot C. Capecitabine and mitomycin C in patients with metastatic colorectal cancer resistant to fluorouracil and irinotecan. Br J Cancer 2006; 94 (06) 935-936 ; author reply 937
  • 925 Lenz HJ et al. Multicenter phase II and translational study of cetuximab in metastatic colorectal carcinoma refractory to irinotecan, oxaliplatin, and fluoropyrimidines. J Clin Oncol 2006; 24 (30) 4914-4921
  • 926 Jonker DJ, O’Callaghan CJ, Karapetis CS et al. Cetuximab for the Treatment of Colorectal Cancer. N Engl J Med 2007; 357: 2040-2048
  • 927 Lievre A et al. KRAS mutations as an independent prognostic factor in patients with advanced colorectal cancer treated with cetuximab. J Clin Oncol 2008; 26 (03) 374-379
  • 928 Hecht JR et al. Panitumumab monotherapy in patients with previously treated metastatic colorectal cancer. Cancer 2007; 110 (05) 980-988
  • 929 Van Cutsem E et al. Open-label phase III trial of panitumumab plus best supportive care compared with best supportive care alone in patients with chemotherapy-refractory metastatic colorectal cancer. J Clin Oncol 2007; 25 (13) 1658-1664
  • 930 Amado RG, Wolf M, Peeters M et al. Wild-Type KRAS Is Required for Panitumumab Efficacy in Patients With Metastatic Colorectal Cancer. Journal of Clinical Oncology 2008; 26 (10) 1626-1634
  • 931 Lehnert T, Golling M. Posterior pelvic exenteration in locoregional recurrence of rectal carcinoma – indications, technique and outcome. Chirurg 2001; 72 (12) 1393-1401
  • 932 Shibata D et al. Surgical management of isolated retroperitoneal recurrences of colorectal carcinoma. Dis Colon Rectum 2002; 45 (06) 795-801
  • 933 Wu JS et al. Meta-analysis of dose-fractionation radiotherapy trials for the palliation of painful bone metastases. Int J Radiat Oncol Biol Phys 2003; 55 (03) 594-605
  • 934 Farnell GF et al. Brain metastases from colorectal carcinoma. The long term survivors. Cancer 1996; 78 (04) 711-716
  • 935 Schoeggl A et al. Stereotactic radiosurgery for brain metastases from colorectal cancer. Int J Colorectal Dis 2002; 17 (03) 150-155
  • 936 Enblad P et al. The risk of subsequent primary malignant diseases after cancers of the colon and rectum. A nationwide cohort study. Cancer 1990; 65 (09) 2091-2100
  • 937 Cali RL et al. Cumulative incidence of metachronous colorectal cancer. Dis Colon Rectum 1993; 36 (04) 388-393
  • 938 Hermanek PJr et al. Long-term results of surgical therapy of colon cancer. Results of the Colorectal Cancer Study Group. Chirurg 1994; 65 (04) 287-297
  • 939 Yamazaki T et al. What is the risk factor for metachronous colorectal carcinoma?. Dis Colon Rectum 1997; 40 (08) 935-938
  • 940 Hemminki K, Li X, Dong C. Second primary cancers after sporadic and familial colorectal cancer. Cancer Epidemiol Biomarkers Prev 2001; 10 (07) 793-798
  • 941 Green RJ et al. Surveillance for second primary colorectal cancer after adjuvant chemotherapy: an analysis of Intergroup 0089. Ann Intern Med 2002; 136 (04) 261-269
  • 942 Harris GJ et al. Factors affecting local recurrence of colonic adenocarcinoma. Dis Colon Rectum 2002; 45 (08) 1029-1034
  • 943 Merkel S et al. Late locoregional recurrence in rectal carcinoma. Eur J Surg Oncol 2002; 28 (07) 716-722
  • 944 Poulin EC et al. Local recurrence and survival after laparoscopic mesorectal resection forrectal adenocarcinoma. Surg Endosc 2002; 16 (06) 989-995
  • 945 Bulow S et al. Recurrence and survival after mesorectal excision for rectal cancer. Br J Surg 2003; 90 (08) 974-980
  • 946 Secco GB et al. Factors influencing incidence and extension of metachronous liver metastases of colorectal adenocarcinoma. A multivariate analysis. Hepatogastroenterology 1997; 44 (16) 1057-1062
  • 947 Pietra N et al. Risk factors of local recurrence of colorectal cancer: a multivariate study. Hepatogastroenterology 1998; 45 (23) 1573-1578
  • 948 Scholmerich J. Sense and nonsense in after-care of colorectal carcinoma. Med Klin (Munich) 1996; 91 (06) 420-427
  • 949 Kievit J. Colorectal cancer follow-up: a reassessment of empirical evidence on effectiveness. Eur J Surg Oncol 2000; 26 (04) 322-328
  • 950 Kievit J. Follow-up of patients with colorectal cancer: numbers needed to test and treat. Eur J Cancer 2002; 38 (07) 986-999
  • 951 Wichmann MW et al. Results of long-term follow-up after curative resection of Dukes A colorectal cancer. World J Surg 2002; 26 (06) 732-736
  • 952 Yamamoto S et al. Postsurgical surveillance for recurrence of UICC stage I colorectal carcinoma: is follow-up by CEA justified?. Hepatogastroenterology 2005; 52 (62) 444-449
  • 953 Korner H et al. Systematic follow-up after curative surgery for colorectal cancer in Norway: a population-based audit of effectiveness, costs, and compliance. J Gastrointest Surg 2005; 9 (03) 320-328
  • 954 Talbot IC et al. The clinical significance of invasion of veins by rectal cancer. Br J Surg 1980; 67 (06) 439-442
  • 955 Minsky BD et al. Resectable adenocarcinoma of the rectosigmoid and rectum. II. The influence of blood vessel invasion. Cancer 1988; 61 (07) 1417-1424
  • 956 Krasna MJ et al. Vascular and neural invasion in colorectal carcinoma. Incidence and prognostic significance. Cancer 1988; 61 (05) 1018-1023
  • 957 Inoue T et al. Vascular invasion of colorectal carcinoma readily visible with certain stains. Dis Colon Rectum 1992; 35 (01) 34-39
  • 958 Bruinvels DJ et al. Follow-up of patients with colorectal cancer. A meta-analysis. Ann Surg 1994; 219 (02) 174-182
  • 959 Rosen M et al. Follow-up of colorectal cancer: a meta-analysis. Dis Colon Rectum 1998; 41 (09) 1116-1126
  • 960 Jeffery GM, Hickey BE, Hider P. Follow-up strategies for patients treated for non-metastatic colorectal cancer. Cochrane Database Syst Rev 2002; 1: CD002200
  • 961 Renehan AG et al. Impact on survival of intensive follow up after curative resection for colorectal cancer: systematic review and meta-analysis of randomised trials. Bmj 2002; 324 (7341) 813
  • 962 Makela JT, Laitinen SO, Kairaluoma MI. Five-year follow-up after radical surgery for colorectal cancer. Results of a prospective randomized trial. Arch Surg 1995; 130 (10) 1062-1067
  • 963 Ohlsson B et al. Follow-up after curative surgery for colorectal carcinoma. Randomized comparison with no follow-up. Dis Colon Rectum 1995; 38 (06) 619-626
  • 964 Kjeldsen BJ et al. A prospective randomized study of follow-up after radical surgery for colorectal cancer. Br J Surg 1997; 84 (05) 666-669
  • 965 Pietra N et al. Role of follow-up in management of local recurrences of colorectal cancer: a prospective, randomized study. Dis Colon Rectum 1998; 41 (09) 1127-1133
  • 966 Schoemaker D et al. Yearly colonoscopy, liver CT, and chest radiography do not influence 5-year survival of colorectal cancer patients. Gastroenterology 1998; 114 (01) 7-14
  • 967 Secco GB et al. Efficacy and cost of risk-adapted follow-up in patients after colorectal cancer surgery: a prospective, randomized and controlled trial. Eur J Surg Oncol 2002; 28 (04) 418-423
  • 968 Jeffery M, Hickey BE, Hider PN. Follow-up strategies for patients treated for non-metastatic colorectal cancer. Cochrane Database Syst Rev 2007; 1: CD002200
  • 969 Wattchow DA et al. General practice vs. surgical-based follow-up for patients with colon cancer: randomised controlled trial. Br J Cancer 2006; 94 (08) 1116-1121
  • 970 Rodriguez-Moranta F et al. Postoperative surveillance in patients with colorectal cancer who have undergone curative resection: a prospective, multicenter, randomized, controlled trial. J Clin Oncol 2006; 24 (03) 386-393
  • 971 Laubert T et al. Intensified surveillance after surgery for colorectal cancer significantly improves survival. Eur J Med Res 2010; 15 (01) 25-30
  • 972 Papagrigoriadis S, Heyman B. Patients’ views on follow up of colorectal cancer: implications for risk communication and decision making. Postgrad Med J 2003; 79 (933) 403-407
  • 973 Cooper GS, TD Kou, HL ReynoldsJr. Receipt of guideline-recommended follow-up in older colorectal cancer survivors: a population-based analysis. Cancer 2008; 113 (08) 2029-2037
  • 974 Rocklin MS, Slomski CA, Watne AL. Postoperative surveillance of patients with carcinoma of the colon and rectum. Am Surg 1990; 56 (01) 22-27
  • 975 Benson 3rd AB et al. 2000 update of American Society of Clinical Oncology colorectal cancer surveillance guidelines. J Clin Oncol 2000; 18 (20) 3586-3588
  • 976 Berman JM, Cheung RJ, Weinberg DS. Surveillance after colorectal cancer resection. Lancet 2000; 355 (9201) 395-399
  • 977 Desch CE et al. Recommended colorectal cancer surveillance guidelines by the American Society of Clinical Oncology. J Clin Oncol 1999; 17 (04) 1312
  • 978 Macdonald JS. Carcinoembryonic antigen screening: pros and cons. Semin Oncol 1999; 26 (05) 556-560
  • 979 Duffy MJ et al. Clinical utility of biochemical markers in colorectal cancer: European Group on Tumour Markers (EGTM) guidelines. Eur J Cancer 2003; 39 (06) 718-727
  • 980 Duffy MJ. Carcinoembryonic antigen as a marker for colorectal cancer: is it clinically useful?. Clin Chem 2001; 47 (04) 624-630
  • 981 Moertel CG et al. An evaluation of the carcinoembryonic antigen (CEA) test for monitoring patients with resected colon cancer. Jama 1993; 270 (08) 943-947
  • 982 Safi F, Beyer HG. The value of follow-up after curative surgery of colorectal carcinoma. Cancer Detect Prev 1993; 17 (03) 417-424
  • 983 Zeng Z, Cohen AM, Urmacher C. Usefulness of carcinoembryonic antigen monitoring despite normal preoperative values in node-positive colon cancer patients. Dis Colon Rectum 1993; 36 (11) 1063-1068
  • 984 Huebner RH et al. A meta-analysis of the literature for whole-body FDG PET detection of recurrent colorectal cancer. J Nucl Med 2000; 41 (07) 1177-1189
  • 985 Annovazzi A et al. 18-fluorodeoxyglucose positron emission tomography in nonendocrine neoplastic disorders of the gastrointestinal tract. Gastroenterology 2003; 125 (04) 1235-1245
  • 986 Ahlquist DA et al. Accuracy of fecal occult blood screening for colorectal neoplasia. A prospective study using Hemoccult and HemoQuant tests. Jama 1993; 269 (10) 1262-1267
  • 987 Hunerbein M et al. The role of transrectal ultrasound-guided biopsy in the postoperative follow-up of patients with rectal cancer. Surgery 2001; 129 (02) 164-169
  • 988 Mitry E et al. Epidemiology, management and prognosis of colorectal cancer with lung metastases: a 30-year population-based study. Gut 2010; 59 (10) 1383-1388
  • 989 Desch CE et al. Colorectal cancer surveillance: 2005 update of an American Society of Clinical Oncology practice guideline. J Clin Oncol 2005; 23 (33) 8512-8519
  • 990 Chau I et al. The value of routine serum carcino-embryonic antigen measurement and computed tomography in the surveillance of patients after adjuvant chemotherapy for colorectal cancer. J Clin Oncol 2004; 22 (08) 1420-1429
  • 991 Sugarbaker PH et al. A simplified plan for follow-up of patients with colon and rectal cancer supported by prospective studies of laboratory and radiologic test results. Surgery 1987; 102 (01) 79-87
  • 992 Wang T et al. The role of postoperative colonoscopic surveillance after radical surgery for colorectal cancer: a prospective, randomized clinical study. Gastrointest Endosc 2009; 69 (03) 609-615
  • 993 Rulyak SJ et al. Outcome of follow-up colon examination among a population-based cohort of colorectal cancer patients. Clin Gastroenterol Hepatol 2007; 5 (04) 470-476 ; quiz 407
  • 994 Rex DK et al. Guidelines for colonoscopy surveillance after cancer resection: a consensus update by the American Cancer Society and the US Multi-Society Task Force on Colorectal Cancer. Gastroenterology 2006; 130 (06) 1865-1871
  • 995 Bouvier AM et al. The lifelong risk of metachronous colorectal cancer justifies long-term colonoscopic follow-up. Eur J Cancer 2008; 44 (04) 522-527
  • 996 Sobhani I et al. Early detection of recurrence by 18FDG-PET in the follow-up of patients with colorectal cancer. Br J Cancer 2008; 98 (05) 875-880
  • 997 Selvaggi F et al. FGD-PET in the follow-up of recurrent colorectal cancer. Colorectal Dis 2003; 5 (05) 496-500
  • 998 Eckardt VF, Bernhard G. Nachsorge beim kolorektalen Karzinom. Eine Analyse von Effektivität und Kosten. Deutsches Ärzteblatt 1997; 94: A456-A462
  • 999 Schwibbe G. Changes in quality of life in oncological patients in the course of an inpatient after-care program. Rehabilitation (Stuttg) 1991; 30 (02) 55-62
  • 1000 Gartner U et al. Physical complaints, stress and quality of life of oncologic patients. Effects and patient assessment in inpatient rehabilitation. Med Klin (Munich) 1996; 91 (08) 501-508
  • 1001 Etzioni DA, El-Khoueiry AB, Beart Jr RW . Rates and predictors of chemotherapy use for stage III colon cancer: a systematic review. Cancer 2008; 113 (12) 3279-3289
  • 1002 Grothey A, Kellermann L, Schmoll HJ. Deficits in management of patients with colorectal carcinoma in Germany. Results of multicenter documentation of therapy algorithms. Med Klin (Munich) 2002; 97 (05) 270-277
  • 1003 von der Schulenburg JM, Prenzler A, Schurer W. Cancer management and reimbursement aspects in Germany: an overview demonstrated by the case of colorectal cancer. Eur J Health Econ 2010; 10 (Suppl. 01) S21-S26
  • 1004 Adler G, Seufferlein T. Hope and disappointment in cancer medicine. Z Arztl Fortbild Qualitatssich 2007; 101 (05) 287-292
  • 1005 Harrison JD et al. What are the unmet supportive care needs of people with cancer? A systematic review. Support Care Cancer 2009; 17: 1117-1128
  • 1006 Lewis R et al. Nurse-led vs. conventional physician-led follow-up for patients with cancer: systematic review. J Adv Nurs 2009; 65 (04) 706-723
  • 1007 Howell DM et al. A mixed-method evaluation of nurse-led community-based supportive cancer care. Support Care Cancer 2008; 16 (12) 1343-1352
  • 1008 Ouwens M et al. Implementation of integrated care for patients with cancer: a systematic review of interventions and effects. Int J Qual Health Care 2009; 21 (02) 137-144
  • 1009 Jahn P et al. Reduction of chemotherapy-induced anorexia, nausea, and emesis through a structured nursing intervention: a cluster-randomized multicenter trial. Support Care Cancer 2009; 17 (12) 1543-1552
  • 1010 Jahn P et al. Improvement of pain related self management for oncologic patients through a trans institutional modular nursing intervention: protocol of a cluster randomized multicenter trial. Trials 2010; 11: 29
  • 1011 Chen RC et al. Patient-reported acute gastrointestinal symptoms during concurrent chemoradiation treatment for rectal cancer. Cancer 2010; 116 (08) 1879-1886
  • 1012 Meyerhardt JA et al. Impact of body mass index and weight change after treatment on cancer recurrence and survival in patients with stage III colon cancer: findings from Cancer and Leukemia Group B 89803. J Clin Oncol 2008; 26 (25) 4109-4115
  • 1013 Meyerhardt JA et al. Physical activity and survival after colorectal cancer diagnosis. J Clin Oncol 2006; 24 (22) 3527-3534
  • 1014 Meyerhardt JA et al. Impact of physical activity on cancer recurrence and survival in patients with stage III colon cancer: findings from CALGB 89803. J Clin Oncol 2006; 24 (22) 3535-3541
  • 1015 Ng K et al. Multivitamin use is not associated with cancer recurrence or survival in patients with stage III colon cancer: findings from CALGB 89803. J Clin Oncol 2010; 28 (28) 4354-4363
  • 1016 Stumpf C et al. Retrospektive Untersuchung zur Therapie mit Mistelextrakten bei Patienten mit kolorektalem Karzinom. Dtsch Zschr Onkol 2007; 39: 12-22
  • 1017 Friedel W et al. Fermented Europaen mistletoe (Viscum album L.) extract in supportive care in patients with primary non-metastatic colorectal cancer. In: Scheer R, , et al., (eds.) Die Mistel in der Tumortherapie. Essen: KVC Verlag; 2009: 563-576
  • 1018 Kienle GS, Kiene H. Review article: Influence of Viscum album L (European mistletoe) extracts on quality of life in cancer patients: a systematic review of controlled clinical studies. Integr Cancer Ther 2010; 9 (02) 142-157
  • 1019 Shimizu M et al. (-)-Epigallocatechin gallate suppresses azoxymethane-induced colonic premalignant lesions in male C57BL/KsJ-db/db mice. Cancer Prev Res (Phila) 2008; 1 (04) 298-304
  • 1020 Hoensch H et al. Prospective cohort comparison of flavonoid treatment in patients with resected colorectal cancer to prevent recurrence. World J Gastroenterol 2008; 14 (14) 2187-2193
  • 1021 Ito K et al. Long-term effect of 5-fluorouracil enhanced by intermittent administration of polysaccharide K after curative resection of colon cancer. A randomized controlled trial for 7-year follow-up. Int J Colorectal Dis 2004; 19 (02) 157-164
  • 1022 Sakamoto J et al. Efficacy of adjuvant immunochemotherapy with polysaccharide K for patients with curatively resected colorectal cancer: a meta-analysis of centrally randomized controlled clinical trials. Cancer Immunol Immunother 2006; 55 (04) 404-411
  • 1023 Kassab S et al. Homeopathic medicines for adverse effects of cancer treatments. Cochrane Database Syst Rev 2009; 2: CD004845
  • 1024 Rahbari NN et al. Definition and grading of anastomotic leakage following anterior resection of the rectum: a proposal by the International Study Group of Rectal Cancer. Surgery 2010; 147 (03) 339-351
  • 1025 Vasen HF et al. New clinical criteria for hereditary nonpolyposis colorectal cancer (HNPCC, Lynch syndrome) proposed by the International Collaborative group on HNPCC. Gastroenterology 1999; 116 (06) 1453-1456