Cervical HPV infection and neoplasia in a large population-based prospective study: the Manchester cohort

被引:188
作者
Peto, J
Gilham, C
Deacon, J
Taylor, C
Evans, C
Binns, W
Haywood, M
Elanko, N
Coleman, D
Yule, R
Desai, M
机构
[1] Univ London London Sch Hyg & Trop Med, Dept Epidemiol & Populat Hlth, London WC1E 7HT, England
[2] Inst Canc Res, Canc Res UK Epidemiol & Genet Unit, Sutton SM2 5NG, Surrey, England
[3] Liverpool Womens Hosp, Cerv Screening QA Reference Ctr, Liverpool L8 7SS, Merseyside, England
[4] Univ London Imperial Coll Sci Technol & Med, Eric Bywaters Ctr, Rheumatol Sect, London W12 0NN, England
[5] Univ London St Georges Hosp, Sch Med, Med Genet Unit, London SW17 0RE, England
[6] Fac Med, Dept Histopathol & Cytol, London W12 0NN, England
[7] Manchester Royal Infirm, Manchester Cytol Ctr, Manchester M13 9WW, Lancs, England
关键词
cervical neoplasia; CIN3; HPV; cervical screening; cohort study;
D O I
10.1038/sj.bjc.6602049
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Cytology and histology records and cervical samples for HPV assay were obtained from a prospective cohort of 49 655 women attending clinics for routine cervical cytology in or near Manchester between 1988 and 1993. The women were followed up for cytological abnormality and neoplasia through the cytology laboratory's records. HPV at entry was assayed in an age- and period-stratified random sample of 7278 women and in prevalent and incident CIN3 cases. The prevalence of newly diagnosed CIN3 increased with time since last normal smear, indicating that most cases persist for several years. CIN3 prevalence did not increase further for screening intervals exceeding 5 years, however, suggesting that CIN3 eventually regresses cytologically. CIN2 prevalence increased less steeply with screening interval, while the prevalence of lesser abnormality was almost independent of screening interval. The prevalence of oncogenic HPV at entry declined from 19% among women aged under 25 to less than 3% at age 40 or above. Oncogenic HPV infection was strongly predictive of subsequent CIN3 (OR 17.2, 95% CI 10.4-28.4), but only weakly related to CIN2 (OR 2.3, 95% CI 0.5-10.7) and lesser abnormality (OR 1.4, 95% CI 0.8-2.5). At current incidence rates, the lifetime risk of developing CIN3 will be 9% in this population. The cumulative risk of CIN3 diagnosis among cytologically normal women with oncogenic HPV detected at entry was 28% (CI 18-43%) after 14 years. Persistence of oncogenic HPV may be more sensitive and specific than cytology for early detection of CIN3 and invasive cancer.
引用
收藏
页码:942 / 953
页数:12
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