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DOI: 10.1055/s-0031-1280313
© Georg Thieme Verlag KG Stuttgart · New York
Mammakarzinom 2011 – Neue Aspekte
Breast Cancer 2011 – New AspectsPublikationsverlauf
eingereicht 28.9.2011
akzeptiert 24.10.2011
Publikationsdatum:
23. November 2011 (online)

Zusammenfassung
Die Behandlungsoptionen und ebenfalls die Charakteristika zur Therapieentscheidung der Patientin mit einem primären und fortgeschrittenen Mammakarzinom werden immer vielfältiger. Neue zielgerichtete Therapien in Kombination mit etablierten Chemotherapien erweitern das Spektrum, doch potenziell vielversprechende Kombinationen erzielen nicht immer ein besseres Ergebnis. Neuste Daten aus der Pharmakogenomik weisen auf Prognose- und Prädiktivfaktoren hin, die nicht nur die Eigenschaften des Tumors, sondern außerdem die vererbbaren genetischen Eigenschaften der Patientin berücksichtigen. Die aktuelle Therapieentscheidung ist somit mittlerweile eine Kombination aus klassischerweise klinischen und modernen molekularen Biomarkern. Immer häufiger werden zusätzlich gesundheitsökonomische Aspekte berücksichtigt, sodass außerdem gesundheitspolitische Überlegungen eine Rolle spielen können. Diese Übersichtsarbeit baut auf den aktuellen Kongressen auf, die jedes Jahr stattfinden. Der letzte berücksichtigte ist hierbei die Jahrestagung der American Society of Clinical Oncology (ASCO) 2011 in Chicago.
Abstract
The treatment options for primary and metastatic breast cancer patients as well as the characteristics considered for therapy decision continue to become more diverse. New target therapies in combination with established chemotherapy regimens extend the range, however, potentially promising combinations do not always result in a benefit for the patient. Latest pharmacogenomics results hint towards prognosis and predictive factors, which do not only focus on the individual properties of the tumor, they also consider the hereditary genetics of the patient. As a result, state of the art therapy decision includes classical clinical as well as modern molecular biomarkers, however, pharmacoeconomic aspects continue to increase in importance in physicians' treatment algorithms. This review builds on the recent congresses, which present new data on the treatment of breast cancer. The last included one is the Annual Meeting of the American Society of Clinical Oncology (ASCO) 2011.
Schlüsselwörter
Mammakarzinom - Therapie - Prognose - molekulare Marker - Studien
Key words
breast cancer - therapy - prognosis - molecular marker - studies
Literatur
- 1
Kaufmann M, Rody A.
Breast cancer: reduced mortality by early detection and adjuvant therapy.
Geburtsh Frauenheilk.
2009;
69
218-232
MissingFormLabel
- 2
Beckmann M W, Blohmer J U, Costa S D et al.
Zurich consensus: German expert opinion on the St. Gallen votes on 15 March 2009 (11th
international conference at St. Gallen: primary therapy of early breast cancer) 2009
St. Gallen conference: primary therapy of early breast cancer – opinion among German
experts (Zurich 2009).
Geburtsh Frauenheilk.
2009;
69
377-383
MissingFormLabel
- 3
Diel I, Dresemann G, Fehm T et al.
Interdisciplinary consensus on the use of adjuvant bisphosphonate therapy in breast
cancer patients.
Geburtsh Frauenheilk.
2009;
69
511-516
MissingFormLabel
- 4
Ruckhaberle E, Solbach C, Kaufmann M.
Conference report on the 31st annual San Antonio breast cancer symposium, December
10-14, 2008 “Continuing change in diagnostics and therapy of breast cancers – from
molecular basics to tailored therapy”.
Geburtsh Frauenheilk.
2009;
69
202-211
MissingFormLabel
- 5
Ruckhaberle E, Rody A, Kaufmann M.
Report of the 32nd annual San Antonio breast cancer symposium, December 10-13, 2009
“An international scientific symposium for interaction and exchange among basic scientists
and clinicians in breast cancer”.
Geburtsh Frauenheilk.
2010;
70
177-183
MissingFormLabel
- 6
Fasching P A, Fehm T, Janni W et al.
Breast cancer therapy – a state of the art review.
Geburtsh Frauenheilk.
2010;
70
875-886
MissingFormLabel
- 7
Kast K, Distler W, Schmutzler R.
Current recommendations for the prevention and treatment of hereditary breast cancer.
Geburtsh Frauenheilk.
2010;
70
634-639
MissingFormLabel
- 8
Goss P E, Ingle J N, Alés-Martínez J E et al.
Exemestane for primary prevention of breast cancer in postmenopausal women: NCIC CTG
MAP.3 – A randomized, placebo-controlled trial.
J Clin Oncol.
2011;
29
(Suppl.)
Abstr. LBA 504
MissingFormLabel
- 9
Goss P E, Ingle J N, Alés-Martínez J E et al.
Exemestane for breast-cancer prevention in postmenopausal women.
N Engl J Med.
2011;
364
(25)
2381-2391
MissingFormLabel
- 10
Meindl A, Ditsch N, Kast K et al.
Familiäres Mamma- und Ovarialkarzinom.
Dtsch Arztebl Int.
2011;
108
(19)
323-330
MissingFormLabel
- 11
Rebbeck T R, Friebel T, Wagner T et al.
Effect of short-term hormone replacement therapy on breast cancer risk reduction after
bilateral prophylactic oophorectomy in BRCA1 and BRCA2 mutation carriers: the PROSE
study group.
J Clin Oncol.
2005;
23
7804-7810
MissingFormLabel
- 12
Petru E, Wildt L, Stummvoll W et al.
Consensus of the Austrian Society for Gynecology and Obstetrics/Gynecologic Oncology
Working Group. Fertility, contraception and hormone replacement therapy in oncologic
patients with special reference to breast cancer.
Geburtsh Frauenheilk.
2009;
69
1071-1077
MissingFormLabel
- 13
Domchek S M, Friebel T, Neuhausen S L et al.
PROSE Consortium: Is hormone replacement therapy (HRT) following risk-reducing salpingo-oophorectomy
(RRSO) in BRCA1 (B1)- and BRCA2 (B2)-mutation carriers associated with an increased
risk of breast cancer?.
J Clin Oncol.
2011;
29
(Suppl.): Abstr 1501
MissingFormLabel
- 14 TIME healthland .(6.6.2011). Im Internet:. http://healthland.time.com/2011/06/06/a-breast-cancer-treatment-works-as-prevention-too Stand: 15.6.2011
MissingFormLabel
- 15
Whelan T J, Olivotto I, Ackerman I et al.
NCIC-CTG MA.20: An intergroup trial of regional nodal irradiation in early breast
cancer.
J Clin Oncol.
2011;
29
(Suppl.): Abstr LBA1003
MissingFormLabel
- 16
Untch M, Fasching P A, Konecny G E et al.
Pathologic complete response after neoadjuvant chemotherapy plus trastuzumab predicts
favorable survival in human epidermal growth factor receptor 2-overexpressing breast
cancer: Results from the TECHNO trial of the AGO and GBG study groups.
J Clin Oncol.
2011;
29
3351-3357
MissingFormLabel
- 17
Gianni L, Eiermann W, Semiglazov V et al.
Neoadjuvant chemotherapy with trastuzumab followed by adjuvant trastuzumab versus
neoadjuvant chemotherapy alone, in patients with HER2-positive locally advanced breast
cancer (the NOAH trial): a randomised controlled superiority trial with a parallel
HER2-negative cohort.
Lancet.
2010;
375
377-384
MissingFormLabel
- 18
Wolff A C, Hammond M E, Schwartz J N et al.
American Society of Clinical Oncology/College of American Pathologists guideline recommendations
for human epidermal growth factor receptor 2 testing in breast cancer.
Arch Pathol Lab Med.
2007;
131
18-43
MissingFormLabel
- 19
Liedtke C, Wolf M K, Kiesel L.
New concepts for targeted systemic therapy in breast cancer.
Geburtsh Frauenheilk.
2010;
70
625-633
MissingFormLabel
- 20
Liedtke C, Kiesel L.
Basal/triple negative breast cancer.
Geburtsh Frauenheilk.
2009;
69
309-315
MissingFormLabel
- 21
Gluz O, Liedtke C, Nitz U et al.
Molecular mechanisms of chemoresistance and potential means of overcoming it.
Geburtsh Frauenheilk.
2009;
69
138-144
MissingFormLabel
- 22
Alba E, Chacon J I, Lluch A et al.
Chemotherapy (CT) with or without carboplatin as neoadjuvant treatment in patients
with basal-like breast cancer: GEICAM 2006-03-A multicenter, randomized phase II study.
J Clin Oncol.
2011;
29
(Suppl.): Abstr 1015
MissingFormLabel
- 23
Gerber B, Eidtmann H, Rezai M et al.
Neoadjuvant bevacizumab and anthracycline-taxane-based chemotherapy in 686 triple-negative
primary breast cancers: Secondary endpoint analysis of the GeparQuinto study (GBG
44).
J Clin Oncol.
2011;
29
(Suppl.): Abstr 1006
MissingFormLabel
- 24
von Minckwitz G, Eidtmann H, Rezai M et al.
Neoadjuvant chemotherapy with or without Bevacizumab: Primary efficacy endpoint analysis
of the GEPARQUINTO Study (GBG 44).
SABCS.
2010;
Abstract
S4-S6
MissingFormLabel
- 25
Bear H D, Tang G, Rastogi P et al.
The effect on pCR of bevacizumab and/or antimetabolites added to standard neoadjuvant
chemotherapy: NSABP protocol B-40.
J Clin Oncol.
2011;
29
(Suppl.): Abstr LBA1005
MissingFormLabel
- 26
Gianni L, Pienkowski T, Im Y H et al.
Neoadjuvant pertuzumab (P) and trastuzumab (H): antitumor and safety analysis of a
randomized phase II study (‘NeoSphere ).
Cancer Res.
2010;
70
82s
MissingFormLabel
- 27
Baselga J, Bradbury I, Eidtmann H et al.
First results of the NeoALTTOtrial (BIG 01-06/EGF 106903): a phase III, randomized,
open label, neoadjuvant study of lapatinib, trastuzumab, and their combination plus
paclitaxel in women with HER 2-positive primary breastcancer.
Cancer Res.
2010;
70
82s
MissingFormLabel
- 28
Guarneri V, Frassoldati A, Bottini A et al.
Final results of a phase II randomized trial of neoadjuvant anthracycline-taxane chemotherapy
plus lapatinib, trastuzumab, or both in HER2-positive breast cancer (CHER-LOB trial).
J Clin Oncol.
2011;
29
(Suppl.): Abstr 507
MissingFormLabel
- 29
Chang J C N, Mayer I A, Forero-Torres A et al.
TBCRC006: A multicenter phase II study of neoadjuvant lapatinib and trastuzumab in
patients with HER2-overexpressing breast cancer.
J Clin Oncol.
2011;
29
(Suppl.): Abstr 505
MissingFormLabel
- 30
Holmes F A, Nagarwala Y M, Espina V A et al.
Correlation of molecular effects and pathologic complete response to preoperative
lapatinib and trastuzumab, separately and combined prior to neoadjuvant breast cancer
chemotherapy.
J Clin Oncol.
2011;
29
(Suppl.): Abstr 506
MissingFormLabel
- 31
Felici A, Verweij J, Sparreboom A.
Dosing strategies for anticancer drugs: the good, the bad and body-surface area.
Eur J Cancer.
2002;
38
(13)
1677-1684
MissingFormLabel
- 32
Saarto T, Blomqvist C, Rissanen P et al.
Haematological toxicity: a marker of adjuvant chemotherapy efficacy in stage II and
III breast cancer.
Br J Cancer.
1997;
75
(2)
301-305
MissingFormLabel
- 33
Poikonen P, Saarto T, Lundin J et al.
Leucocyte nadir as a marker for chemotherapy efficacy in node-positive breast cancer
treated with adjuvant CMF.
Br J Cancer.
1999;
80
(11)
1763-1766
MissingFormLabel
- 34
Mayers C, Panzarella T, Tannock I F.
Analysis of the prognostic effects of inclusion in a clinical trial and of myelosuppression
on survival after adjuvant chemotherapy for breast carcinoma.
Cancer.
2001;
91
2246-2257
MissingFormLabel
- 35
Cameron D A, Massie C, Kerr G et al.
Moderate neutropenia with adjuvant CMF confers improved survival in early breast cancer.
Br J Cancer.
2003;
89
(10)
1837-1842
MissingFormLabel
- 36
Gurney H.
Dose calculation of anticancer drugs: a review of the current practice and introduction
of an alternative.
J Clin Oncol.
1996;
14
(9)
2590-2611
MissingFormLabel
- 37
Bergh J, Wiklund T, Erikstein B et al.
Tailored fluorouracil, epirubicin and cyclophosphamide compared with marrow-supported
high-dose chemotherapy as adjuvant treatment for high-risk breast cancer: a randomised
trial. Scandinavian Breast Group 9401 study.
Lancet.
2000;
356
(9239)
1384-1391
MissingFormLabel
- 38
Lindman H, Aström G, Ahlgren J et al.
Individually tailored toxicity-based 5-fluorouracil, epirubicin and cyclophosphamide
(FEC) therapy of metastatic breast cancer.
Acta Oncol.
2007;
46
(2)
165-171
MissingFormLabel
- 39
Iiristo M, Wiklund T, Wilking N et al.
Tailored chemotherapy doses based on toxicity in breast cancer result in similar quality
of life values, irrespective of given dose levels.
Acta Oncol.
2011;
50
338-343
MissingFormLabel
- 40
Lindman H, Andersson M, Edlund P et al.
A randomized study of individually tailored toxicity-based dosage of lluorouracil-epirubicin-cyclophosphamide
chemotherapy (FEC) for early breast cancer (SBG 2000-1).
J Clin Oncol.
2011;
29
(Suppl.): Abstr 1017
MissingFormLabel
- 41
Edlund P, Ahlgren J, Bjerre K et al.
Dose-tailoring of FEC adjuvant chemotherapy based on leukopenia is feasible and well
tolerated. Toxicity and dose intensity in the Scandinavian Breast Group phase 3 adjuvant
Trial SBG 2000-1.
Acta Oncol.
2011;
50
(3)
329-337
MissingFormLabel
- 42
Citron M L, Berry D A, Cirrincione C et al.
Randomized trial of dose-dense versus conventionally scheduled and sequential versus
concurrent combination chemotherapy as postoperative adjuvant treatment of node-positive
primary breast cancer: first report of Intergroup Trial C9741/Cancer and Leukemia
Group B Trial 9741.
J Clin Oncol.
2003;
21
(8)
1431-1439
MissingFormLabel
- 43
Moebus V, Jackisch C, Lueck H et al.
Intense dose-dense sequential chemotherapy with epirubicin, paclitaxel, and cyclophosphamide
compared with conventionally scheduled chemotherapy in high-risk primary breast cancer:
mature results of an AGO phase III study.
J Clin Oncol.
2010;
28
(17)
2874-2880
MissingFormLabel
- 44
Moebus V, Thomssen C, Lueck H et al.
Intense dose-dense (idd) sequential chemotherapy with epirubicin (E), paclitaxel (T),
and cyclophosphamide (C) (ETC) compared with conventionally scheduled chemotherapy
in high-risk breast cancer patients (> 3+LN): Eight-year follow-up analysis.
J Clin Oncol.
2011;
29
(Suppl.): Abstr 1018
MissingFormLabel
- 45
Moebus V, Lueck H, Thomssen C et al.
The impact of epoetin-alpha on anemia, red blood cell (RBC) transfusions, and survival
in breast cancer patients (pts) treated with dose-dense sequential chemotherapy: Mature
results of an AGO phase III study (ETC trial).
J Clin Oncol 2007; ASCO Annual Meeting Proceedings Part I.
2007;
25
(Suppl.)
569
MissingFormLabel
- 46
Giordano S H, Lin Y, Kuo Y et al.
Anthracyline (A) use among women with breast cancer (BC).
J Clin Oncol.
2011;
29
(Suppl.): Abstr 1019
MissingFormLabel
- 47
Cheang M C U, Voduc D, Tu D et al.
The responsiveness of intrinsic subtypes to adjuvant anthracyclines versus nonanthracyclines
in NCIC.CTG MA.5 randomized trial.
J Clin Oncol.
2011;
29
(Suppl.): Abstr 1032
MissingFormLabel
- 48
Rocca A, Paradiso A, Sismondi P et al.
Benefit from CMF with or without anthracyclines in relation to biologic profiles in
early breast cancer.
J Clin Oncol.
2011;
29
(Suppl.): Abstr 1031
MissingFormLabel
- 49
Somlo G.
Discussion: Triple-negative/Cytotoxics/Local Therapy.
J Clin Oncol.
2011;
(suppl.; discussion)
MissingFormLabel
- 50
Henderson I C.
Can we abandon anthracyclines for early breast cancer patients?.
Oncology.
2011;
25
(2)
115-124
127
MissingFormLabel
- 51 NCCN-Guidelines™ Version 2.2011 Breast Cancer. Im Internet: http://www.nccn.org/professionals/physician_gls/f_guidelines.asp%23site Stand: 15.6.2011
MissingFormLabel
- 52 AGO-Leitlinie Mamma: Adjuvante Chemotherapie + Trastuzumab (Optimale Substanzen/Dosierung/Trastuzumab). Im Internet: http://www.ago-online.de/_download/unprotected/g_mamma_11_1_0_d_03_adjuvant_chemotherapy.pdf Stand: 15.6.2011
MissingFormLabel
- 53
Gonzalez-Angulo A M, Litton J K, Broglio K R et al.
High risk of recurrence for patients with breast cancer who have human epidermal growth
factor receptor 2-positive, node-negative tumors 1 cm or smaller.
J Clin Oncol.
2009;
27
(34)
5700-5706
MissingFormLabel
- 54
Piccart-Gebhart M J, Procter M, Leyland-Jones B et al.
Herceptin adjuvant (HERA) trial study team. Trastuzumab after adjuvant chemotherapy
in HER2-positive breast cancer.
N Engl J Med.
2005;
353
(16)
1659-1672
MissingFormLabel
- 55
Romond E H, Perez E A, Bryant J et al.
Trastuzumab plus adjuvant chemotherapy for operable HER2-positive breast cancer.
N Engl J Med.
2005;
353
(16)
1673-1684
MissingFormLabel
- 56
Joensuu H, Isola J, Lundin M et al.
Amplification of erbB2 and erbB2 expression are superior to estrogen receptor status
as risk factors for distant recurrence in pT1N0M0 breast cancer: a nationwide population-based
study.
Clin Cancer Res.
2003;
(3)
923-930
MissingFormLabel
- 57
Rakkhit R et al.
Significant increased recurrence rates among breast cancer patients with HER2-positive,
T1a,bN0M0 tumors.
Cancer Res.
2009;
69
(Suppl.)
96
Abstr 701
MissingFormLabel
- 58
Amar S, McCullough A E, Tan W et al.
Prognosis and outcome of small (≤ 1 cm), node-negative breast cancer on the basis
of hormonal and HER-2 status.
Oncologist.
2011;
15
1043-1049
MissingFormLabel
- 59
Amar S, McCullough A E, Tan W et al.
Prognosis and outcome of small (<=1 cm), node-negative breast cancer on the basis
of hormonal and HER-2 status.
Oncologist.
2010;
15
(10)
1043-1049
MissingFormLabel
- 60
Tovey S M et al.
Poor survival outcomes in HER2-positive breast cancer patients with low-grade, node-negative
tumours.
Br J Cancer.
2009;
100
(5)
680-683
MissingFormLabel
- 61
Pagani A et al.
Clinical outcome of very small (< 1 cm) HER2-positive breast cancer and the role of
trastuzumab as adjuvant treatment.
Ann Oncol.
2008;
19
ix87-ix102
Abstr. L2
MissingFormLabel
- 62
Norris B, Chia S, Cheang M et al.
Poor 10-year breast cancer – specific survival and relapsefree survival for HER2-positive
T1N0 tumors.
Breast Cancer Res Treat.
2006;
100
S90
MissingFormLabel
- 63
Chia S et al.
Human epidermal growth factor receptor 2 overexpression as a prognostic factor in
a large tissue microarray series of node-negative breast cancers.
J Clin Oncol.
2008;
26
5697-5704
MissingFormLabel
- 64
Park Y, Kim S, Ok O et al.
Risk stratification by hormonal receptor (ER, PgR) and HER2 status in small (≤ 1 cm)
invasive breast cancer: Who might be a possible candidate for adjuvant treatment?.
J Clin Oncol.
2009;
27
(Suppl.)
15
Abstr 564
MissingFormLabel
- 65
Chew H K, Brown M.
Cause-specific and all-cause mortality of HER2-positive, node-negative, T1a and T1b
breast cancers.
J Clin Oncol.
2010;
28
(Suppl.)
15
Abstr 583
MissingFormLabel
- 66
Dall P, Hinke A, Lenzen G et al.
Adjuvant treatment strategy and results in small breast cancer tumours (pT1) with
HER2 overexpression.
J Clin Oncol.
2011;
29
(Suppl.): Abstr 607
MissingFormLabel
- 67
Wassermann J, Albiges L, Rodrigues M J et al.
Treatment of small node-negative HER2+ invasive breast carcinomas: Forty-month update
of the joint Aerio/Remagus study.
J Clin Oncol.
2011;
29
(Suppl.): Abstr 557
MissingFormLabel
- 68
Rodrigues M J, Wassermann J, Albiges L et al.
Trastuzumab treatment in T1ab, node-negative, human epidermal growth factor receptor
2-overexpressing breast carcinomas.
J Clin Oncol.
2010;
28
(28)
e541-542
MissingFormLabel
- 69
Fehrenbacher L, Shiraz P, Sattavat M et al.
T1abN0M0 HER2+ invasive breast cancer recurrence: Population-based cohort of 17,000
+ consecutive breast cancers 2000–2006 at Kaiser Permanente Northern California (KPNC).
J Clin Oncol.
2011;
29
(Suppl.): Abstr 551
MissingFormLabel
- 70
Cancello G, Maisonneuve P, Rotmensz N et al.
Prognosis in women with small (T1mic, T1a, T1b) node-negative operable breast cancer
by immunohistochemically selected subtypes.
J Clin Oncol.
2011;
29
(Suppl.): Abstr 546
MissingFormLabel
- 71
O'Brien N A, Browne B C, Chow L et al.
Activated phosphoinositide 3-kinase/AKT signaling confers resistance to trastuzumab
but not lapatinib.
Mol Cancer Ther.
2010;
9
(6)
1489-1502
MissingFormLabel
- 72
Stemke-Hale K, Gonzalez-Angulo A M, Lluch A et al.
An integrative genomic and proteomic analysis of PIK3CA, PTEN, and AKT mutations in
breast cancer.
Cancer Res.
2008;
68
(15)
6084-6091
MissingFormLabel
- 73
Saal L H, Johansson P, Holm K et al.
Poor prognosis in carcinoma is associated with a gene expression signature of aberrant
PTEN tumor suppressor pathway activity.
Proc Natl Acad Sci USA.
2007;
104
(18)
7564-7569
MissingFormLabel
- 74
Nagata Y, Lan K H, Zhou X et al.
PTEN activation contributes to tumor inhibition by trastuzumab, and loss of PTEN predicts
trastuzumab resistance in patients.
Cancer Cell.
2004;
6
(2)
117-127
MissingFormLabel
- 75
Dave B, Migliaccio I, Gutierrez M C et al.
Loss of phosphatase and tensin homolog or phosphoinositol-3 kinase activation and
response to trastuzumab or lapatinib in human epidermal growth factor receptor 2-overexpressing
locally advanced breast cancers.
J Clin Oncol.
2011;
29
(2)
166-173
MissingFormLabel
- 76
Esteva F J, Guo H, Zhang S et al.
PTEN, PIK3CA, p-AKT, and p-p 70S6K status: association with trastuzumab response and
survival in patients with HER2-positive metastatic breast cancer.
Am J Pathol.
2010;
177
(4)
1647-1656
MissingFormLabel
- 77
Fabi A, Metro G, Di Benedetto A et al.
Clinical significance of PTEN and p-Akt co-expression in HER2-positive metastatic
breast cancer patients treated with trastuzumab-based therapies.
Oncology.
2010;
78
(2)
141-149
MissingFormLabel
- 78
Gori S, Sidoni A, Colozza M et al.
EGFR, pMAPK, pAkt and PTEN status by immunohistochemistry: correlation with clinical
outcome in HER2-positive metastatic breast cancer patients treated with trastuzumab.
Ann Oncol.
2009;
20
(4)
648-654
MissingFormLabel
- 79
Yonemori K, Tsuta K, Shimizu C et al.
Immunohistochemical expression of PTEN and phosphorylated Akt are not correlated with
clinical outcome in breast cancer patients treated with trastuzumab-containing neo-adjuvant
chemotherapy.
Med Oncol.
2009;
26
(3)
344-349
MissingFormLabel
- 80
Perez E A, Suman V J, Davidson N E et al.
Results of chemotherapy alone, with sequential or concurrent addition of 52 weeks
of trastuzumab in the NCCTG N9831 HER2-positive adjuvant breast cancer Trial.
Cancer Res.
2009;
69
(Suppl.): Abstr 80
MissingFormLabel
- 81
Perez E A, Reinholz M M, Hillman D W et al.
HER2 and chromosome 17 effect on patient outcome in the N9831 adjuvant trastuzumab
trial.
J Clin Oncol.
2010;
28
(28)
4307-4315
MissingFormLabel
- 82
Perez E A, Dueck A C, Reinholz M M et al.
Effect of PTEN protein expression on benefit to adjuvant trastuzumab in early-stage
HER2+ breast cancer in NCCTG adjuvant trial N9831.
J Clin Oncol.
2011;
29
(Suppl.): Abstr 10504
MissingFormLabel
- 83
Martin M, Martinez N, Ramos M et al.
Randomized, phase II trial comparing continuous versus intermittent capecitabine (X)
monotherapy for metastatic breast cancer (MBC): Results from the GEICAM 2009-05 study.
J Clin Oncol.
2011;
29
(Suppl.): Abstr 1008
MissingFormLabel
- 84
Gluz O, Liedtke C, Kates R E et al.
Molecular subtypes, body mass index (BMI), and their time-varying prognostic impact
in node-positive breast cancer (BC): Pooled analysis from the WSG AM-01 and -02 trials.
J Clin Oncol.
2011;
29
(Suppl.): Abstr 1021
MissingFormLabel
- 85
Pfeiler G, Königsberg R, Mlineritsch B et al.
Effect of change of body mass index (BMI) during therapy on the efficacy of endocrine
therapy in premenopausal patients with breast cancer: An analysis of the ABCSG-12
trial.
J Clin Oncol.
2011;
29
(Suppl.): Abstr 514
MissingFormLabel
- 86
Dawood S S, Lei X, Litton J K et al.
Effect of body mass index on survival outcome among women with early-stage, triple-negative
breast cancer.
J Clin Oncol.
2011;
29
(Suppl.): Abstr 1130
MissingFormLabel
- 87
Gennari A, Puntoni M, Nanni O et al.
Body mass index (BMI) and prognosis in women with metastatic breast cancer (MBC).
J Clin Oncol.
2011;
29
(Suppl.): Abstr 566
MissingFormLabel
- 88
Giuliano M, Giordano A, Patt A et al.
Circulating tumor cells as a prognostic factor independent of obesity in metastatic
breast cancer patients.
J Clin Oncol.
2011;
29
(Suppl.): Abstr 610
MissingFormLabel
- 89
Gnant M, Mlineritsch B, Schippinger W et al.
Endocrine therapy plus zoledronic acid in premenopausal breast cancer.
N Engl J Med.
2009;
360
679-691E
MissingFormLabel
- 90
Eidtmann H, de Boer R, Bundred N et al.
Efficacy of zoledronic acid in postmenopausal women with early breast cancer receiving
adjuvant letrozole: 36-month results of the ZO-FAST Study.
Ann Oncol.
2010;
21
2188
MissingFormLabel
- 91
Coleman R E, Thorpe H C, Cameron D et al.
AZURE (BIG 01/01) investigators. Adjuvant treatment with Zoledronic acid in stage
II/III breast cancer. The AZURE trial (BIG 01/04).
SABCS.
2010;
Abstr 4–5
MissingFormLabel
- 92
Gnant M, Mlineritsch B, Stoeger H et al.
Overall survival with adjuvant zoledronic acid in patients with premenopausal breast
cancer with complete endocrine blockade: Long-term results from ABCSG-12.
J Clin Oncol.
2011;
29
(Suppl.): Abstr 520
MissingFormLabel
- 93
De la Haba J, Rodriguez-Lescure A, Baena J M et al.
Final analysis of dose density with zoledronic acid treatment in metastatic breast
cancer patients: ZARAS study.
J Clin Oncol.
2011;
29
(Suppl.): Abstr 630
MissingFormLabel
- 94
De Censi A, Sun Z, Thurlimann B J K et al.
Bone mineral density (BMD) in participants (pts) of trial BIG 1-98 comparing adjuvant
letrozole (L) versus tamoxifen (T) or their sequence.
J Clin Oncol.
2011;
29
(Suppl.): Abstr 516
MissingFormLabel
- 95
Perrone F, Gallo C, Lastoria S et al.
Bone effects of adjuvant tamoxifen (T), letrozole (L), or L plus zoledronic acid (Z)
in early breast cancer (EBC): The phase III HOBOE study.
J Clin Oncol.
2011;
29
(Suppl.): Abstr 517
MissingFormLabel
- 96
Hershman D L, Cheung A M, Chapman J W et al.
Effects of adjuvant exemestane versus anastrozole on bone mineral density: Two-year
results of the NCIC CTG MA.27 bone companion study.
J Clin Oncol.
2011;
29
(Suppl.): Abstr 518
MissingFormLabel
- 97
Enright K, Trudeau M E, Taback N et al.
A population-based assessment of the risk of fragility fracture associated with the
use of adjuvant hormone therapy for early breast cancer in older women.
J Clin Oncol.
2011;
29
(Suppl.): Abstr 519
MissingFormLabel
- 98
Batouli P, Jahanshahi J B Y.
Global cancer mortality: The effect of health care system resources on survival from
cancer.
J Clin Oncol.
2011;
29
(Suppl.): Abstr 1576
MissingFormLabel
- 99
Hassett M J, Neville B A, Weeks J C.
The relationship between cost, quality, and outcomes among women with breast cancer
in SEER–Medicare.
J Clin Oncol.
2011;
29
(Suppl.): Abstr 6001
MissingFormLabel
- 100
Negro E G, Rivarola J, Gil E et al.
Off-label prescriptions in cancer: Who should pay for them?.
J Clin Oncol.
2011;
29
(Suppl.): Abstr e16559
MissingFormLabel
- 101
Touloukian E Z, Yakan A, Bloom R E.
Antiemetic choice based on economic advantage.
J Clin Oncol.
2011;
29
(Suppl.): Abstr 9018
MissingFormLabel
- 102
Garrison L P, Lalla D, Brammer M G et al.
Assessing the potential cost-effectiveness of retesting IHC0, IHC1-positive, or FISH-negative
early-stage breast cancer patients for HER2 status.
J Clin Oncol.
2011;
29
(Suppl.): Abstr 6133
MissingFormLabel
- 103
Deenen M J, Cats A, Sechterberger M K et al.
Safety, pharmacokinetics (PK), and cost-effectiveness of upfront genotyping of DPYD
in fluoropyrimidine therapy.
J Clin Oncol.
2011;
29
(Suppl.): Abstr 3606
MissingFormLabel
- 104
Nearchou D, Valachis A, Polyzos N P et al.
Conflict of interest in economic analyses of targeted therapies in oncology.
J Clin Oncol.
2011;
29
(Suppl.): Abstr 6120
MissingFormLabel
- 105
Carter J A, Snedecor S J, Kaura S et al.
Cost-effectiveness of zoledronic acid (ZOL) versus denosumab (Dmab) in prevention
of skeletal-related events (SREs) in metastatic breast cancer (mBC).
J Clin Oncol.
2011;
29
(Suppl.): Abstr 9025
MissingFormLabel
- 106
Coyle D, Grunfeld E, Coyle K et al.
Cost-effectiveness of a survivorship care plan for breast cancer survivors.
J Clin Oncol.
2011;
29
(Suppl.): Abstr 6082
MissingFormLabel
S. Kümmel
Kliniken Essen-Mitte
Evang. Huyssens-Stiftung/Knappschaft GmbH
Henricistraße 92
45136 Essen
eMail: s.kuemmel@kliniken-essen-mitte.de