Die meisten Zervixkarzinome sind auf die HPV (humane Papillomviren)-Genotypen
16 oder 18, anogenitale Warzen fast immer auf die HPV-Genotypen
6 oder 11 zurückzuführen. In placebokontrollierten
Studien ließen sich Infektionen und assoziierte klinische
Läsionen durch einen Impfstoff gegen HPV (6, 11, 16, 18)
bei primär nicht infizierten Frauen nahezu vollständig
verhindern. Neue Daten zeigen jedoch, dass auch Frauen, die sexuell
aktiv sind bzw. bereits eine Infektion durchgemacht haben, von der
Impfung profitieren. Diese Ergebnisse implizieren den Nutzen einer
generellen HPV-Impfung bei sexuell aktiven Frauen.
Summary
Most cervical cancers are caused by human papillomavirus (HPV)
genotypes 16 or 18, while almost all the anogenital warts are related
to HPV 6 and 11. In placebo-controlled trials, a vaccine against
HPV (6, 11, 16, 18) almost completely prevented infections and associated
clinical lesions in primarily not infected women. Furthermore, new
data demonstrate that sexually active women, as well as those with
prior infection, also benefit from the vaccine. These results suggest
that a general vaccination programme for sexually active women will
be beneficial.
2
Evander M, Edlund K, Gustafsson A. et al .
Human papillomavirus infection is transient in young women:
a population-based cohort study.
J Infect Dis.
1995;
171
1026-1030
3 Ferris D, Garland S. for the Quadrivalent HPV Vaccine Investigators .Evaluation of quadrivalent HPV 6/11/16/18
vaccine efficacy against cervical and anogenital disease in subjects
with prior vaccine HPV type infection. Kuala Lumpur (Malaysia); 13th International Congress on Infectious Diseases 19.-22. Juni 2008
4
Garland S M, Hernandez-Avila M, Wheeler C M, Perez G, Harper D M, Leodolter S. et al .
Quadrivalent vaccine against
human papillomavirus to prevent anogenital disease.
N
Engl J Med.
2007;
356
1928-19435
5
Harper. et al .
Sustained
immunogenicity and high efficacy against HPV-16/18 related
cervical neoplasia: Long-term follow up through 6.4 years in women
vaccinated with Cervarix (GSK’s HPV 16/18 AS04 candidate
vaccine).
Gynecol Oncol.
2008;
109
158-159
6
Ho G YF, Bierman R, Beardsley L, Chang C J, Burk R D.
Natural history of cervicovaginal papillomavirus infection in
young women.
N Engl J Med.
1998;
338
423-438
8
Joura E A, Leodolter S, Hernandez-Avila M, Wheeler C M, Perez C, Koutsky L A. et al .
Efficacy of a
quadrivalent prophylactic human papillomavirus (types 6,11, 16,18)L1
virus-like particle vaccine against high-grade vulval and vaginal
lesions: a combined analysis of three clinical trials.
Lancet.
2007;
369
1693-1702
9
Kjaer S K, Breugelmanns G, Munk, Junge J, Watson M, Iftner T.
Population- based prevalence, type- and age-specific distribution
of HPV in women before introduction of an HPV-vaccination program
in Denmark.
Int J Cancer.
2008;
123
1864-1870
10 Lacey C JN. for
the Gardasil Phase III Investigators .Continued efficacy of
quadrivalent HPV (types 6/11/16/18) L1
VLP vaccine in preventing cervical or external genital disease:
4 years of follow-up. Lissabon, Portugal; 20th
European College of Obstetrics and Gynecology 4.-8. März
2008
11
Melnikow J, Nuovo J, Willan A R. et
al .
Natural history of cervical squamous intraepithelial
lesions: a meta-analysis.
Obstet Gynecol.
1998;
92
727-735
12
Munoz N, Bosch F X, de Sanjose S. et al .
International Agency for Research on Cancer Multicenter Cervical
Study Group: Epidemiological classification of human papillomavirus
types associated with cervical cancer.
N Engl J Med.
2003;
348
518-527
13
Munoz N, Bosch F X, Castellsagué X. et
al .
Against which human papillomavirus types shall
we vaccinate and screen? The international perspective.
Int
J Cancer.
2004;
111
278-285
14
Paavonen J. and the
FUTURE II Study Group .
Baseline demographic characteristics
of subjects enrolled in international quadrivalent HPV (types 6/11/16/18)
vaccine clinical trials.
Curr Med Res Opin.
2008;
24
1623-1634
16
Robert-Koch-Institut .
Impfung
gegen humane Papillomaviren (HPV) für Mädchen
von 12 bis 17 Jahren – Empfehlung und Begründung.
Epidemiologisches Bulletin.
2007;
12
97-103
17
Pathirana D, Hillemanns P, Petry K -U, Becker N, Brockmeyer N H, Erdmann R. et al .
S3-Leitlinie zur Impfprävention
HPV-assoziierter Neoplasien.
Chemother J.
2008;
17
120-128
18
Paavonen J, Jenkins D, Bosch F X, Naud P, Salmerón J. et
al .
Efficacy of a prophylactic adjuvanted bivalent
L1 virus-like-particle vaccine against infection with human papillomavirus
types 16 and 18 in young women: an interim analysis of a phase III
double-blind, randomised controlled trial.
Lancet.
2007;
369
2161-70
19
Siegrist C A. et
al .
Human Papillomavirus Immunization in adolescent and
young adults.
The Pediatric Infectious Disease Journal.
2007;
26
(11)
979-84
20
The FUTURE II Study Group .
Quadrivalent
vaccine against human papillomavirus to prevent high-grade cervical
lesions.
N Engl J Med.
2007;
356
1915-1927
21
The FUTURE II Study Group .
Prophylactic
efficacy of a quadrivalent human papillomavirus (HPV) vaccine in
women with virological evidence of HPV infection.
J Infect
Dis.
2007;
196
1438-1446
22 Verstraeten. et al .Analysis of adverse events of potential autoimmune aetiology
in a large integrated safety database of AS04 adjuvant vaccines. Vaccine 2008, Oct 7 (published online
ahead)
23
Villa L L, Costa RL LR, Petta C A, Andrade R P, Ault K A, Giuliano A R. et
al .
Prophylactic quadrivalent human papillomavirus
(types 6, 11, 16, 18) L1 virus-like particle vaccine in young women:
a randomised double-blind placebo-controlled multicentre phase II
efficacy trial.
Lancet Oncol.
2005;
6
271-278
24
Walboomers J MM, Jacobs M V, Manos M M. et al .
Human papillomavirus is
a necessary cause of invasive cervical cancer worldwide.
J
Pathol.
1999;
189
12-19
25
Wiley D J, Douglas J, Beutner K, Cox T, Fife K, Moscicki A B. et al .
External genital warts; diagnosis, treatment
and prevention.
Clin Infect Dis.
2002;
35
(Suppl 2)
S210-224