Schiffman M, Burk R D, Boyle S, Raine-Bennett T, Katki H A, Gage J C, Wentzensen N, Kornegay J R, Aldrich C, Tam T, Erlich H, Apple R, Befano B, Castle P E
National Cancer Institute, Bethesda, Maryland, USA
Albert Einstein College of Medicine, Bronx, New York, New York, USA.
J Clin Microbiol. 2015 Jan;53(1):52-9. doi: 10.1128/JCM.02116-14. Epub 2014 Oct 22.
The effective management of women with human papillomavirus (HPV)-positive, cytology-negative results is critical to the introduction of HPV testing into cervical screening. HPV typing has been recommended for colposcopy triage, but it is not clear which combinations of high-risk HPV types provide clinically useful information. This study included 18,810 women with Hybrid Capture 2 (HC2)-positive, cytology-negative results and who were age ≥30 years from Kaiser Permanente Northern California. The median follow-up was 475 days (interquartile range [IQR], 0 to 1,077 days; maximum, 2,217 days). The baseline specimens from 482 cases of cervical intraepithelial neoplasia grade 3 or cancer (CIN3+) and 3,517 random HC2-positive noncases were genotyped using 2 PCR-based methods. Using the case-control sampling fractions, the 3-year cumulative risks of CIN3+ were calculated for each individual high-risk HPV type. The 3-year cumulative risk of CIN3+ among all women with HC2-positive, cytology-negative results was 4.6%. HPV16 status conferred the greatest type-specific risk stratification; women with HC2-positive/HPV16-positive results had a 10.6% risk of CIN3+, while women with HC-2 positive/HPV16-negative results had a much lower risk of 2.4%. The next most informative HPV types and their risks in HPV-positive women were HPV33 (5.9%) and HPV18 (5.9%). With regard to the etiologic fraction, 20 of 71 cases of cervical adenocarcinoma in situ (AIS) and adenocarcinoma in the cohort were positive for HPV18. HPV16 genotyping provides risk stratification useful for guiding clinical management; the risk among HPV16-positive women clearly exceeds the U.S. consensus risk threshold for immediate colposcopy referral. HPV18 is of particular interest because of its association with difficult-to-detect glandular lesions. There is a less clear clinical value of distinguishing the other high-risk HPV types.
对人乳头瘤病毒(HPV)检测呈阳性但细胞学检查结果为阴性的女性进行有效管理,对于将HPV检测引入宫颈癌筛查至关重要。HPV分型已被推荐用于阴道镜检查分流,但尚不清楚哪些高危HPV类型的组合能提供临床有用信息。本研究纳入了18,810名来自北加利福尼亚州凯撒医疗集团、年龄≥30岁、杂交捕获2代(HC2)检测呈阳性且细胞学检查结果为阴性的女性。中位随访时间为475天(四分位间距[IQR],0至1,077天;最长2,217天)。采用两种基于聚合酶链反应(PCR)的方法,对482例宫颈上皮内瘤变3级或癌症(CIN3+)病例及3,517例随机抽取的HC2检测呈阳性的非病例的基线标本进行基因分型。利用病例对照抽样比例,计算每种高危HPV类型个体的CIN3+三年累积风险。所有HC2检测呈阳性且细胞学检查结果为阴性的女性中,CIN3+的三年累积风险为4.6%。HPV16状态赋予了最大的型特异性风险分层;HC2检测呈阳性/HPV16检测呈阳性的女性发生CIN3+的风险为10.6%,而HC-2检测呈阳性/HPV16检测呈阴性的女性发生CIN3+的风险则低得多,为2.4%。在HPV检测呈阳性的女性中,接下来最具信息价值的HPV类型及其风险分别为HPV33(5.9%)和HPV18(5.9%)。就病因分数而言,该队列中71例宫颈原位腺癌(AIS)和腺癌病例中有20例HPV18检测呈阳性。HPV16基因分型提供的风险分层有助于指导临床管理;HPV16检测呈阳性的女性的风险明显超过美国立即转诊阴道镜检查的共识风险阈值。HPV18因其与难以检测的腺性病变有关而特别受关注。区分其他高危HPV类型的临床价值尚不太明确。