Human Papillomavirus Genotypes From Vaginal and Vulvar Intraepithelial Neoplasia in Females 15-26 Years of Age

被引:2
作者
Garland, Suzanne M.
Joura, Elmar A.
Ault, Kevin A.
Bosch, F. Xavier
Brown, Darron R.
Castellsague, Xavier
Ferenczy, Alex
Ferris, Daron G.
Giuliano, Anna R.
Hernandez-Avila, Mauricio
Huh, Warner K.
Iversen, Ole-Erik
Kjaer, Susanne K.
Kurman, Robert J.
Luna, Joaquin
Monsonego, Joseph
Munoz, Nubia
Paavonen, Jorma
Pitisuttihum, Punnee
Ronnett, Brigitte M.
Steben, Marc
Stoler, Mark H.
Wheeler, Cosette M.
Wiley, Dorothy J.
Perez, Gonzalo
Saah, Alfred J.
Luxembourg, Alain
Li, Se
DiNubile, Mark J.
Wagner, Monika
Velicer, Christine
机构
[1] Univ Melbourne, Royal Womens Hosp,Dept Microbiol Infect Dis, Royal Childrens Hosp Infect & Immun,Dept Microbio, Murdoch Childrens Res Inst,Dept Obstet & Gynaecol, Melbourne, Vic, Australia
[2] Med Univ Vienna, Comprehens Canc Ctr, Dept Gynecol & Obstet, Vienna, Austria
[3] Univ Kansas, Med Ctr, Dept Obstet & Gynecol, Kansas City, KS 66103 USA
[4] IDIBELL, RTICC, CIBER ESP, Inst Catala Oncol, Barcelona, Spain
[5] Indiana Univ, Sch Med, Dept Med, Indianapolis, IN 46204 USA
[6] SMBD Jewish Gen Hosp, Dept Pathol, Montreal, PQ, Canada
[7] McGill Univ, Montreal, PQ, Canada
[8] Augusta Univ, Dept Obstet & Gynecol, Augusta, GA USA
[9] H Lee Moffitt Canc Ctr & Res Inst, Ctr Infect Res Canc, Tampa, FL USA
[10] Natl Inst Publ Hlth, Cuernavaca, Morelos, Mexico
[11] Univ Alabama Birmingham, Div Gynecol Oncol, Birmingham, AL USA
[12] Univ Bergen, Haukeland Univ Hosp, Dept Clin Sci, Bergen, Norway
[13] Danish Canc Soc, Res Ctr, Copenhagen, Denmark
[14] Univ Copenhagen, Rigshosp, Dept Gynecol, Copenhagen, Denmark
[15] Johns Hopkins Univ, Sch Med, Baltimore, MD USA
[16] Fdn Univ Sanitas, Clin Colsanitas, Dept Obstet & Gynecol, Bogota, Colombia
[17] Inst Col, Paris, France
[18] Natl Canc Inst, Bogota, Colombia
[19] Univ Cent Hosp, Dept Obstet & Gynecol, Helsinki, Finland
[20] Mahidol Univ, Fac Trop Med, Bangkok, Thailand
[21] Inst Natl Sante Publ Quebec, Direct Risques Biol & Sante Travail, Montreal, PQ, Canada
[22] Univ Virginia Hlth Syst, Robert E Fechner Lab Surg Pathol, Charlottesville, VA USA
[23] Univ New Mexico, Hlth Sci Ctr, Dept Pathol, Albuquerque, NM 87131 USA
[24] Univ New Mexico, Hlth Sci Ctr, Dept Obstet & Gynecol, Albuquerque, NM 87131 USA
[25] UCLA, Sch Nursing, Los Angeles, CA 90024 USA
[26] Merck & Co Inc, Kenilworth, NJ USA
[27] Univ Rosario, Bogota, Colombia
[28] Analyt LASER, Montreal, PQ, Canada
基金
美国国家卫生研究院;
关键词
ATTRIBUTION; CANCERS; VACCINE; WOMEN; RISK; HPV; PREVALENCE; INFECTION; CARCINOMA; DIAGNOSIS;
D O I
10.1097/AOG.0000000000002736
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
OBJECTIVE: To estimate the proportion of vulvar and vaginal low-grade and high-grade squamous intraepithelial lesions (LSILs and HSILs) in females 15-26 years of age attributable to 14 human papillomavirus (HPV) genotypes (6, 11, 16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59). METHODS: A post hoc analysis of prospectively diagnosed vulvar and vaginal LSILs and HSILs among females 15-26 years of age enrolled in the placebo arms of two phase 3, randomized HPV vaccine trials assessed 14 prespecified HPV genotypes associated with cervical cancers or anogenital warts using a type-specific multiplex polymerase chain reaction assay. The frequency of lesions associated with specific HPV genotypes was estimated by proportional and other attribution methods. RESULTS: During approximately 4 years of follow-up in 8,798 females, 40 vulvar LSILs and 46 vulvar HSILs were diagnosed in 68 females, and 118 vaginal LSILs and 33 vaginal HSILs were diagnosed in 107 females. Females developing vulvar (41.2%) or vaginal (49.5%) lesions also had cervical lesions, whereas 6.5% of females with cervical lesions had vaginal or vulvar lesions. At least 1 of the 14 HPV genotypes was detected in females with vulvar LSIL (72.5%), vulvar HSIL (91.3%), vaginal LSIL (61.9%), and vaginal HSIL (72.7%). Considering only HPV-positive lesions, the nine most common genotypes causing cervical cancer and anogenital warts (6, 11, 16, 18, 31, 33, 45, 52, and 58) were found in 89.4% of vulvar LSILs, 100% of vulvar HSILs, 56.0% of vaginal LSILs, and 78.3% of vaginal HSILs. CONCLUSION: Most vulvar and vaginal lesions were attributable to at least 1 of the 14 HPV genotypes analyzed. Effective immunization programs could potentially prevent substantial numbers of HPV-related vulvar and vaginal LSILs and HSILs.
引用
收藏
页码:261 / 270
页数:10
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