Department of Cancer Epidemiology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100021, China.
Department of Pathology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100021, China.
Int J Cancer. 2019 Jan 1;144(1):34-42. doi: 10.1002/ijc.31633. Epub 2018 Oct 26.
The management of HPV-positive women becomes particularly crucial in cervical cancer screening. Here we assessed whether detection of E6 or E7 oncoproteins targeting eight most prevalent HPV types could serve as a promising triage option. Women (N = 1,416) aged 50-60 from Shanxi, China underwent screening with HPV testing and liquid-based cytology (LBC), with any positive results referring to colposcopy and biopsy if necessary. Women with HPV-positive results received further tests using DNA-based genotyping, E6 or E7 oncoprotein detection targeting HPV16/18 (for short: E6 (16/18) Test) or HPV16/18/31/33/35/45/52/58 (for short: E6/E7 (8 types) Test), respectively. Among HPV-positive women, E6/E7 (8 types) oncoproteins had lower positivity (17.37%) compared to DNA-based genotyping for same eight types (58.30%) and LBC with ASC-US threshold (50.97%); HPV16 was the genotype showing the highest frequency (8.49%) for oncoprotein detection followed by HPV52 (3.47%), 58 (2.32%), 33 (1.54%), 18 (1.16%), 45 (0.77%), 35 (0.39%) and 31 (0%). For detection of cervical intraepithelial neoplasia Grade 3 or higher (CIN3+), E6/E7 (8 types) Test had similar sensitivity (100.00%) and superior specificity (85.94%) as well as positive predictive value (PPV, 22.22%) compared to both LBC and DNA-based genotyping (8 types); For detection of CIN2+, E6/E7 (8 types) Test was less sensitive (67.74%) but still more specific (89.47%) and risk predictive with PPV of 46.67%. Notably, E6/E7 (8 types) Test remarkably decreased the number of colposcopies needed to detect one CIN2+ and CIN3+ (2.14 and 4.50). E6/E7 oncoprotein detection showed a good "trade-off" between sensitivity and specificity with more efficient colposcopy referrals, which is of great importance to maximize the benefits of HPV-based screening program, especially applicable for the areas with high HPV prevalence and low-resources.
HPV 阳性女性的管理在宫颈癌筛查中尤为重要。在这里,我们评估了针对最常见的 8 种 HPV 类型的 E6 或 E7 癌蛋白检测是否可作为一种有前途的分流选择。来自中国山西的 50-60 岁女性接受了 HPV 检测和液基细胞学(LBC)筛查,如果结果为阳性,则进行阴道镜检查和活检。HPV 阳性结果的女性进一步接受了基于 DNA 的基因分型、针对 HPV16/18 的 E6 或 E7 癌蛋白检测(简称 E6(16/18) 检测)或针对 HPV16/18/31/33/35/45/52/58 的 E6/E7(8 种类型)癌蛋白检测(简称 E6/E7(8 种类型) 检测)。在 HPV 阳性女性中,E6/E7(8 种类型) 癌蛋白的阳性率(17.37%)低于针对相同 8 种类型的 DNA 基因分型(58.30%)和 ASC-US 阈值的 LBC(50.97%);HPV16 是癌蛋白检测中频率最高的基因型(8.49%),其次是 HPV52(3.47%)、58(2.32%)、33(1.54%)、18(1.16%)、45(0.77%)、35(0.39%)和 31(0%)。对于检测宫颈上皮内瘤变 3 级或更高(CIN3+),E6/E7(8 种类型) 检测的敏感性(100.00%)和特异性(85.94%)以及阳性预测值(PPV,22.22%)与 LBC 和 DNA 基因分型(8 种类型)相似;对于检测 CIN2+,E6/E7(8 种类型) 检测的敏感性较低(67.74%),但特异性(89.47%)和风险预测仍较高,PPV 为 46.67%。值得注意的是,E6/E7(8 种类型) 检测显著减少了发现一个 CIN2+和 CIN3+所需的阴道镜检查数量(分别为 2.14 和 4.50)。E6/E7 癌蛋白检测在敏感性和特异性之间表现出良好的“平衡”,并能更有效地进行阴道镜检查转诊,这对于最大限度地提高 HPV 筛查计划的效益非常重要,特别是在 HPV 流行率高且资源有限的地区。