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Clinical Performance of Human Papillomavirus Testing and Visual Inspection With Acetic Acid in Primary, Combination, and Sequential Cervical Cancer Screening in China

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机构: [1]Univ Chicago, Pritzker Sch Med, Chicago, IL 60637 USA [2]NIH, UJMT Fogarty Consortium, Fogarty Int Ctr, Bldg 10, Bethesda, MD 20892 USA [3]Univ Texas Southwestern, Dept Psychiat, Dallas, TX USA [4]Chinese Acad Med Sci, Canc Hosp, Dept Epidemiol, Natl Canc Ctr, Beijing, Peoples R China [5]Peking Union Med Coll, Beijing, Peoples R China [6]Capital Med Ctr, Beijing Tongren Hosp, Dept Gynecol, Beijing, Peoples R China [7]CAMS, Canc Hosp, Natl Canc Ctr, Dept Pathol, Beijing, Peoples R China [8]Inner Mongolia Autonomous Reg Peoples Hosp, Dept Pathol, Hohhot, Inner Mongolia, Peoples R China [9]Univ N Carolina, Gillings Sch Global Publ Hlth, Dept Epidemiol, Chapel Hill, NC 27515 USA [10]Univ N Carolina, UNC Lineberger Comprehens Canc Ctr, Chapel Hill, NC 27515 USA
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Background World Health Organization guidelines recommend screening with human papillomavirus (HPV) testing followed by either treatment of all HPV-positives, or by visual inspection (VIA) for triage to treatment, citing insufficient evidence to recommend either strategy over the other. Methods We assessed VIA and HPV testing individually, in combination (HPV-VIA cotesting), and as triage models. Three thousand women were screened in Inner Mongolia, China, concurrently with HPV testing and VIA in a real population setting. Screen-positive women underwent colposcopy, and biopsy, if indicated. Accuracy of screening algorithms for cervical intraepithelial neoplasia grade 2 or higher (CIN-2+) was calculated after controlling for verification bias. HPV testing followed by VIA triage for CIN-2+ detection was compared with Hybrid Capture 2 viral loads triage, measured in relative light units/cutoff. Results CIN-2+ prevalence was 1.0%. Corrected sensitivity, false negative rate, and specificity for CIN-2+, respectively, for primary HPV testing were 89.7%, 10.3%, and 83.3%; 44.8%, 55.2%, and 92 center dot 3% for VIA; 93.1%, 6.9%, and 80.2% for HPV-VIA cotesting; and 41.4%, 58.6, and 95.4% for HPV with VIA triage scenarios. Using relative light units/cutoff of 5 or greater to triage HPV-positive women had twice the sensitivity as VIA triage, with comparable specificity for CIN-2+. Conclusions When VIA performs relatively poorly and HPV testing is available, adding VIA to sequential (ie, HPV followed by VIA triage) or primary (HPV-VIA cotesting) screening does not significantly improve CIN-2+ detection beyond primary HPV screening alone. Sequential screening (ie, HPV followed by VIA triage) reduces sensitivity too low for population-based screening programs. The HPV viral loads could offer an alternative low-resource country triage strategy.

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出版当年[2018]版:
大类 | 3 区 医学
小类 | 4 区 传染病学
最新[2025]版:
大类 | 4 区 医学
小类 | 4 区 传染病学
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Q3 INFECTIOUS DISEASES
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Q3 INFECTIOUS DISEASES

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第一作者机构: [1]Univ Chicago, Pritzker Sch Med, Chicago, IL 60637 USA [2]NIH, UJMT Fogarty Consortium, Fogarty Int Ctr, Bldg 10, Bethesda, MD 20892 USA [3]Univ Texas Southwestern, Dept Psychiat, Dallas, TX USA
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通讯机构: [9]Univ N Carolina, Gillings Sch Global Publ Hlth, Dept Epidemiol, Chapel Hill, NC 27515 USA [10]Univ N Carolina, UNC Lineberger Comprehens Canc Ctr, Chapel Hill, NC 27515 USA [*1]Univ N Carolina, Gillings Sch Global Publ Hlth, 2101 McGavran Greenberg Hall,CB 7435, Chapel Hill, NC 27599 USA
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