使用阴道和宫颈样本进行hrHPV初筛以检测高级别上皮内病变的临床表现。

Jonathan King, Yvonne N Flores, Joacim Meneses-León, Sonia Hernández-Salazar, Karina Robles-Rivera, Berenice Rivera-Paredez, Leith León-Maldonado, Rubí Hernández-López, Leticia Torres-Ibarra, Eduardo Lazcano-Ponce, Jorge Salmerón
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摘要

高风险人乳头瘤病毒(hrHPV)检测是目前全球最推荐的宫颈癌症筛查的主要方法。临床医生收集的宫颈取样仍然是主要的取样方法,但hrHPV阴道自取样是一种有吸引力的替代方法,因为它具有更大的可接受性和潜在的更高的成本效益。本研究旨在确定hrHPV阴道自采样是否与临床医生收集的宫颈采样可用于检测组织学确诊的高级别宫颈上皮内瘤样病变(CIN2/3),这是墨西哥宫颈癌症筛查计划的一部分。我们分析了5856名在hrHPV筛查研究中筛查的女性的数据。使用三种分型策略:HPV16/18基因分型、HPV16/18/33/58扩展基因分型和HPV16/18/11/33/58扩展基因型,对CIN3和CIN2+终点的两种采样方法的临床表现和诊断效率指标进行了评估。hrHPV阳性在801例(13.7%)宫颈和897例(15.3%)阴道样本中发现。所有hrHPV阳性样本的女性均接受阴道镜检查,在考虑回顾性分诊策略之前,阴道镜共检测到17例CIN3病例。使用HPV16/18/31/33/58扩展基因分型策略,245名妇女的宫颈hrHPV阳性,269名妇女的阴道hrHPV阳性。使用该策略时,在hrHPV阳性宫颈样本的女性和hrHPV阳性阴道样本的女性中各检测到10例CIN3病例,在敏感性和特异性方面没有观察到显著差异。我们观察到,无论使用何种分诊策略,自行和临床医生收集的采样方法在检测CIN3和CIN2+方面都是可比较的。这些发现可以帮助公共卫生官员制定更具成本效益的癌症宫颈筛查计划,最大限度地提高参与度。
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Clinical Performance of hrHPV Primary Screening Using Vaginal versus Cervical Samples to Detect High-grade Intraepithelial Lesions.

High-risk human papillomavirus (hrHPV) testing is now the most recommended primary method for cervical cancer screening worldwide. Clinician-collected cervical sampling continues to be the main sampling method, but hrHPV vaginal self-sampling is an appealing alternative because of its greater acceptability and potentially higher cost-effectiveness. This study aimed to determine whether hrHPV vaginal self-sampling is comparable with clinician-collected cervical sampling for detecting histologically confirmed high-grade cervical intraepithelial neoplasia (CIN2/3) as part of a cervical cancer screening program in Mexico. We analyzed data from 5,856 women screened during a hrHPV-based screening study. Clinical performance and diagnostic efficiency metrics were estimated for the two sampling methods for the CIN3 and CIN2+ endpoints, using three triage strategies: HPV16/18 genotyping, HPV16/18/33/58 extended genotyping, and HPV16/18/31/33/58 extended genotyping. hrHPV-positivity was found in 801 (13.7%) cervical and 897 (15.3%) vaginal samples. All women with hrHPV-positive samples were referred to colposcopy, which detected 17 total CIN3 cases before considering retrospective triage strategies. Using the HPV16/18/31/33/58 extended genotyping strategy, 245 women had hrHPV-positive cervical samples and 269 had hrHPV-positive vaginal samples. Ten CIN3 cases were detected each among women with hrHPV-positive cervical samples and among those with hrHPV-positive vaginal samples when using this strategy, with no significant differences in sensitivity and specificity observed. We observe that self- and clinician-collected sampling methods are comparable for detecting CIN3 and CIN2+ regardless of the triage strategy used. These findings can help public health officials to develop more cost-effective cervical cancer screening programs that maximize participation.

Prevention relevance: We found that hrHPV vaginal self-sampling is comparable with hrHPV clinician cervical sampling when using any triage strategy to refer women to colposcopy, so self-sampling is a viable cervical screening method. Therefore, policymakers should consider incorporating self-sampling into cervical screening programs to increase screening coverage and reduce cervical cancer burden. See related Spotlight, p. 649.

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