The Impact of Quadrivalent Human Papillomavirus (HPV; Types 6, 11, 16, and 18) L1 Virus‐Like Particle Vaccine on Infection and Disease Due to Oncogenic Nonvaccine HPV Types in Generally HPV‐Naive Women Aged 16–26 Years

Darron R. Brown(Indiana University School of Medicine), Susanne K. Kjær(University of Copenhagen), Kristján Sigurðsson(Cancer Clinic), Ole‐Erik Iversen(University of Bergen), Mauricio Hernández-Ávila, Cosette M. Wheeler, Gonzalo Pérez, Laura A. Koutsky(University of Washington), Eng Hseon Tay(KK Women's and Children's Hospital), Patricia García(Universidad Peruana Cayetano Heredia), Kevin A. Ault(Emory University), Suzanne M. Garland(The University of Melbourne), Sepp Leodolter(Medical University of Vienna), Sven‐Eric Olsson(Karolinska Institutet), Grace Tang(University of Hong Kong), Daron G. Ferris(Augusta University), Jorma Paavonen(University of Helsinki), Marc Steben, F. Xavier Bosch(Institut d'Investigació Biomédica de Bellvitge), Joakim Dillner(Lund University), Elmar A. Joura(Johns Hopkins University), Robert J. Kurman(Medical University of Warsaw), Sławomir Majewski(National Cancer Institute), Nubia Muñóz(Duke University), Evan R. Myers, Luisa L. Villa, Frank J. Taddeo, Christine C. Roberts, Amha Tadesse, Janine T. Bryan, Lisa Lupinacci, Katherine Giacoletti, Heather L. Sings(Merck Biopharma Co., Ltd. (Japan)), Margaret K. James, Teresa M. Hesley, Eliav Barr
The Journal of Infectious Diseases
February 23, 2009
Cited by 627Open Access
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Abstract

BACKGROUND: Human papillomavirus (HPV)-6/11/16/18 vaccine reduces the risk of HPV-6/11/16/18-related cervical intraepithelial neoplasia (CIN) 1-3 or adenocarcinoma in situ (AIS). Here, its impact on CIN1-3/AIS associated with nonvaccine oncogenic HPV types was evaluated. METHODS: We enrolled 17,622 women aged 16-26 years. All underwent cervicovaginal sampling and Pap testing at regular intervals for up to 4 years. HPV genotyping was performed for biopsy samples, and histological diagnoses were determined by a pathology panel. Analyses were conducted among subjects who were negative for 14 HPV types on day 1. Prespecified analyses included infection of 6 months' duration and CIN1-3/AIS due to the 2 and 5 most common HPV types in cervical cancer after HPV types 16 and 18, as well as all tested nonvaccine types. RESULTS: Vaccination reduced the incidence of HPV-31/45 infection by 40.3% (95% confidence interval [CI], 13.9% to 59.0%) and of CIN1-3/AIS by 43.6% (95% CI, 12.9% to 64.1%), respectively. The reduction in HPV-31/33/45/52/58 infection and CIN1-3/AIS was 25.0% (95% CI, 5.0% to 40.9%) and 29.2% (95% CI, 8.3% to 45.5%), respectively. Efficacy for CIN2-3/AIS associated with the 10 nonvaccine HPV types was 32.5% (95% CI, 6.0% to 51.9%). Reductions were most notable for HPV-31. CONCLUSIONS: HPV-6/11/16/18 vaccine reduced the risk of CIN2-3/AIS associated with nonvaccine types responsible for approximately 20% of cervical cancers. The clinical benefit of cross-protection is not expected to be fully additive to the efficacy already observed against HPV-6/11/16/18-related disease, because women may have >1 CIN lesion, each associated with a different HPV type. TRIAL REGISTRATION: ClinicalTrials.gov identifiers: NCT00092521 , NCT00092534 , and NCT00092482.


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