Human Papillomavirus Infections and Vulvar Disease Development

被引:29
作者
Garland, Suzanne M. [2 ,3 ]
Insinga, Ralph P. [4 ]
Sings, Heather L. [5 ]
Haupt, Richard M. [6 ]
Joura, Elmar A. [1 ]
机构
[1] Med Univ Vienna, Dept Obstet & Gynecol, Div Gynecol Oncol, Allgemeines Krankenhaus Stadt Wien, A-1090 Vienna, Austria
[2] Royal Hosp Women, Dept Microbiol & Infect Dis, Melbourne, Vic, Australia
[3] Univ Melbourne, Dept Obstet & Gynecol, Melbourne, Vic, Australia
[4] Merck Res Labs, Dept Hlth Econ Stat, N Wales, PA USA
[5] Merck Res Labs, Dept Med Commun, N Wales, PA USA
[6] Merck Res Labs, Dept Vaccines & Biol Clin Res, N Wales, PA USA
关键词
CERVICAL INTRAEPITHELIAL NEOPLASIA; PARTICLE VACCINE; QUADRIVALENT VACCINE; SQUAMOUS CARCINOMA; NATURAL-HISTORY; YOUNG-WOMEN; HPV TYPES; LESIONS; EFFICACY; TYPE-16;
D O I
10.1158/1055-9965.EPI-09-0067
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: We describe the prevalence of 14 common types [human papillomavirus (HPV)-6/11/16/18/31/33/35/39/45/51/52/56/58/591 in vulvar intraepithelial neoplasia grades 1 to 3 (VIN 1-3) and HPV genotype-specific infection in relation to the development of VIN 1-3. Methods: Data were analyzed from women enrolled in the placebo arms of three randomized double-blind trials. Anogenital examinations, including collection of labial/vulvar/perineal/perianal swabs, occurred at day 1 and every 6 to 12 months through 48 months. Lesions that were possibly, probably, or definitely HPV related or of unknown etiology were biopsied. Biopsies and swabs were HPV typed. Biopsies were read for endpoint determination WIN 1-3) by up to four pathologists. Results: Incident infection with HPV-16 was the most common (6.0/100 person-years). The mean time from incident infection to the development of VIN 1-3 was 18.5 months (95% confidence interval, 13.4-23.6). HPV-6 or 11 was observed in 64.5%. of VIN 1 and 29.0% of VIN 2/ 3, whereas HPV-16 was observed in 6.5% of VIN 1 and 64.5% of VIN 2/3. Conclusion: A vaccine that includes both low- and high-risk types could prevent more than half of VIN 1-3 lesions, including the precursor lesions to HPV-related vulvar carcinoma. Understanding the incidence and duration of vulvar HPV infection and risk for progression to VIN 1-3 may inform therapeutic decisions for vulvar disease and mathematical models that assess the cost-effectiveness of vaccination. (Cancer Epidemiol Biomarkers Prev 2009;18(6):1777-84)
引用
收藏
页码:1777 / 1784
页数:8
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