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Human papillomavirus (HPV) DNA triage of women with atypical squamous cells of undetermined significance with cobas 4800 HPV and Hybrid Capture 2 tests for detection of high-grade lesions of the uterine cervix

机译:具有非确定性意义的非典型鳞状细胞的妇女乳头瘤病毒(HPV)DNA分型,使用cobas 4800 HPV和Hybrid Capture 2测试来检测宫颈的高级病变

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摘要

The triage of women with high-risk (HR) human papillomavirus (HPV)-positive smears for atypical squamous cells of undetermined significance (ASC-US) to colposcopy is now an integrated option in clinical guidelines. The performance of cobas 4800 HPV and that of Hybrid Capture 2 (HC2) for HR HPV DNA detection in cervical samples in PreservCyt were compared in 396 women referred to colposcopy for ASC-US. Of these, 316 did not have cervical intraepithelial neoplasia (CIN), 47 had CIN1, 29 had CIN2 or CIN3 (CIN2+), and 4 had CIN of unknown grade. HR HPV was detected in 129 (32.6%) and 149 (37.6%) samples with HC2 and cobas 4800 HPV, respectively (P = 0.15). The clinical sensitivities and specificities for detecting CIN2+ were 89.7% (95% confidence interval [CI], 72.8 to 97.2%) and 66.7% (95% CI, 61.7 to 71.3%) with cobas 4800 HPV and 93.1% (95% CI, 77.0 to 99.2%) and 72.2% (95% CI 67.4 to 76.5%) with HC2. The performance of cobas 4800 HPV was similar to that of HC2 for identifying women with ASC-US who would benefit the most from colposcopy.
机译:对于阴道镜检查,对于具有非确定意义的非典型鳞状细胞(ASC-US),对高危(HR)人乳头瘤病毒(HPV)阳性涂片分流的妇女现已成为临床指南中的综合选择。比较了在PreservCyt宫颈样本中用cobas 4800 HPV和Hybrid Capture 2(HC2)检测HR HPV DNA的性能,在396例因ASC-US进行阴道镜检查的女性中进行了比较。其中,316个没有宫颈上皮内瘤变(CIN),47个有CIN1,29个有CIN2或CIN3(CIN2 +),4个有未知等级的CIN。分别在HC2和cobas 4800 HPV的129个样本中(32.6%)和149个样本(37.6%)检测到HR HPV(P = 0.15)。使用cobas 4800 HPV和93.1%(95%CI,95%CI,95%置信区间[CI]为72.8至97.2%)和66.7%(95%CI为61.7至71.3%)来检测CIN2 +的临床敏感性和特异性。 77.0%至99.2%)和72.2%(95%CI为67.4%至76.5%)。 cobas 4800 HPV的性能与HC2相似,可用于识别ASC-US女性,她们将从阴道镜检查中受益最大。

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