Attribution of 12 High-Risk Human Papillomavirus Genotypes to Infection and Cervical Disease

被引:118
|
作者
Joura, Elmar A. [1 ]
Ault, Kevin A. [2 ]
Bosch, F. Xavier [3 ]
Brown, Darron [4 ]
Cuzick, Jack [5 ]
Ferris, Daron [6 ]
Garland, Suzanne M. [7 ]
Giuliano, Anna R. [8 ]
Hernandez-Avila, Mauricio [9 ]
Huh, Warner [10 ]
Iversen, Ole-Erik [11 ]
Kjaer, Susanne K. [12 ,13 ]
Luna, Joaquin [14 ]
Miller, Dianne [15 ]
Monsonego, Joseph [16 ]
Munoz, Nubia [17 ]
Myers, Evan [18 ]
Paavonen, Jorma [19 ]
Pitisuttithum, Punnee [20 ]
Steben, Marc [21 ]
Wheeler, Cosette M. [22 ,23 ]
Perez, Gonzalo [24 ,25 ]
Saah, Alfred [24 ]
Luxembourg, Alain [24 ]
Sings, Heather L. [24 ]
Velicer, Christine [24 ]
机构
[1] Med Univ Vienna, Dept Gynecol & Obstet, Ctr Comprehens Canc, A-1090 Vienna, Austria
[2] Univ Kansas, Med Ctr, Dept Obstet & Gynecol, Kansas City, KS 66103 USA
[3] IDIBELL, Inst Catala Oncol, Barcelona, Spain
[4] Indiana Univ Sch Med, Dept Med, Indianapolis, IN 46202 USA
[5] Queen Mary Univ London, Wolfson Inst Prevent Med, London, England
[6] Georgia Regents Univ, Dept Obstet & Gynecol, Augusta, GA USA
[7] Univ Melbourne, Dept Obstet & Gynecol, Royal Womens Hosp, Dept Microbiol Infect Dis, Melbourne, Vic 3010, Australia
[8] H Lee Moffitt Canc Ctr & Res Inst, Ctr Infect Res Canc, Tampa, FL USA
[9] Natl Inst Publ Hlth, Cuernavaca, Morelos, Mexico
[10] Univ Alabama Birmingham, Div Gynecol Oncol, Birmingham, AL USA
[11] Univ Bergen, Haukeland Univ Hosp, Inst Clin Med, Bergen, Norway
[12] Danish Canc Soc, Res Ctr, Copenhagen, Denmark
[13] Univ Copenhagen, Rigshosp, Dept Gynecol, DK-1168 Copenhagen, Denmark
[14] Fdn Univ Sanitas, Dept Obstet & Gynecol, Clin Colsanitas, Bogota, Colombia
[15] Univ British Columbia, Dept Obstet & Gynaecol, Vancouver, BC V5Z 1M9, Canada
[16] Inst Col, Paris, France
[17] Natl Canc Inst, Bogota, Colombia
[18] Duke Univ, Med Ctr, Dept Obstet & Gynecol, Durham, NC 27710 USA
[19] Univ Cent Hosp, Dept Obstet & Gynecol, Helsinki, Finland
[20] Mahidol Univ, Fac Trop Med, Bangkok 10700, Thailand
[21] INSERM, Direct Risques Biol & Sante Travail, Montreal, PQ, Canada
[22] Univ New Mexico, Dept Pathol, Hlth Sci Ctr, Albuquerque, NM 87131 USA
[23] Univ New Mexico, Hlth Sci Ctr, Dept Obstet & Gynecol, Albuquerque, NM 87131 USA
[24] Merck & Co Inc, Whitehouse Stn, NJ USA
[25] Univ Rosario, Bogota, Colombia
关键词
GENITAL WARTS; PARTICLE VACCINE; YOUNG-WOMEN; HPV VACCINE; INTRAEPITHELIAL NEOPLASIA; PREVALENCE; EFFICACY; PROGRAM; TYPE-11; IMPACT;
D O I
10.1158/1055-9965.EPI-14-0410
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: We estimated the prevalence and incidence of 14 human papillomavirus (HPV) types (6/11/16/18/31/33/35/39/45/51/52/56/58/59) in cervicovaginal swabs, and the attribution of these HPV types in cervical intraepithelial neoplasia (CIN), and adenocarcinoma in situ (AIS), using predefined algorithms that adjusted for multiple-type infected lesions. Methods: A total of 10,656 women ages 15 to 26 years and 1,858 women ages 24 to 45 years were enrolled in the placebo arms of one of three clinical trials of a quadrivalent HPV vaccine. We estimated the cumulative incidence of persistent infection and the proportion of CIN/AIS attributable to individual carcinogenic HPV genotypes, as well as the proportion of CIN/AIS lesions potentially preventable by a prophylactic 9-valent HPV6/11/16/18/31/33/45/52/58 vaccine. Results: The cumulative incidence of persistent infection with >= 1 of the seven high-risk types included in the 9-valent vaccine was 29%, 12%, and 6% for women ages 15 to 26, 24 to 34, and 35 to 45 years, respectively. A total of 2,507 lesions were diagnosed as CIN or AIS by an expert pathology panel. After adjusting for multiple-type infected lesions, among women ages 15 to 45 years, these seven high-risk types were attributed to 43% to 55% of CIN1, 70% to 78% of CIN2, 85% to 91% of CIN3, and 95% to 100% of AIS lesions, respectively. The other tested types (HPV35/39/51/56/59) were attributed to 23% to 30% of CIN1, 7% to 14% of CIN2, 3% to 4% of CIN3, and 0% of AIS lesions, respectively. Conclusions: Approximately 85% or more of CIN3/AIS, >70% CIN2, and approximately 50% of CIN1 lesions worldwide are attributed to HPV6/11/16/18/31/33/45/52/58. Impact: If 9-valent HPV vaccination programs are effectively implemented, the majority of CIN2 and CIN3 lesions worldwide could be prevented, in addition to approximately one-half of CIN1. (C)2014 AACR.
引用
收藏
页码:1997 / 2008
页数:12
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