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A cocktail of p16INK4a and Ki-67 p16INK4a and minichromosome maintenance protein 2 as triage tests for human papillomavirus primary cervical cancer screening

机译:p16INK4a和Ki-67p16INK4a和微染色体维持蛋白2的混合物作为人乳头瘤病毒原发性宫颈癌筛查的分流测试

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摘要

Most human papillomavirus (HPV) infections are transient and additional triage approaches should be built after HPV-based primary cervical cancer screening. We evaluated the accuracy of p16/Ki-67 and p16/mcm2 dual staining as biomarkers for triaging HPV positive women in China. 4070 participants aged 35 to 64 years attending ongoing cervical cancer screening were enrolled in 2015-2016. Cervical exfoliated cells were collected for HPV DNA analysis and the residual positive specimens were tested for liquid-based cytology and biomarkers. Women infected with HPV 16/18 type or other 12 high-risk HPV types with abnormal cytology results received colposcopy. We found the positive rates of both biomarkers increased significantly with histology severity. p16/Ki-67 positivity in HPV16/18 group, other 12 high-risk HPV group and HPV negative group was 50.0%, 33.7% and 8.9%, respectively. The corresponding p16/mcm2 positivity was 70.0%, 56.3% and 6.7%, respectively. The sensitivity and specificity of p16/Ki-67 for CIN2+ in all HPV-positive women were 91.7% and 63.5%, with a referral rate of 36.2%, while p16/mcm2 were 87.5% and 42.1%, with a referral rate of 58.4%, respectively. The sensitivity of p16/Ki-67 increased to 95.8% for CIN2+ and 100% for CIN3+ when combined with high-grade cytology, without decrease in specificity. Our studies suggest that p16/Ki-67 is an efficient triaging biomarker for HPV-positive women and could reduce colposcopy workload. p16/mcm2 is more sensitive compared with cytology for identifying cervical lesions.
机译:大多数人乳头瘤病毒(HPV)感染是暂时性的,在基于HPV的原发性宫颈癌筛查后应建立其他分类方法。我们评估了p16 / Ki-67和p16 / mcm2双重染色作为对中国HPV阳性女性进行分类的生物标记物的准确性。 2015-2016年招募了4070名年龄在35至64岁之间,正在接受宫颈癌筛查的参与者。收集宫颈脱落细胞用于HPV DNA分析,并对残留的阳性标本进行液基细胞学和生物标记物测试。细胞学结果异常的HPV 16/18型或其他12种高危型HPV感染的妇女接受阴道镜检查。我们发现两种生物标志物的阳性率均随组织学严重程度显着增加。 HPV16 / 18组,其他12个高危HPV组和HPV阴性组的p16 / Ki-67阳性率分别为50.0%,33.7%和8.9%。相应的p16 / mcm2阳性率分别为70.0%,56.3%和6.7%。在所有HPV阳性女性中,p16 / Ki-67对CIN2 +的敏感性和特异性分别为91.7%和63.5%,推荐率为36.2%,而p16 / mcm2分别为87.5%和42.1%,推荐率为58.4。 %, 分别。与高级细胞学结合使用时,p16 / Ki-67的敏感性对CIN2 +的敏感性提高到95.8%,对CIN3 +的敏感性提高到100%,而特异性没有降低。我们的研究表明,p16 / Ki-67是HPV阳性女性的有效分诊生物标志物,可以减少阴道镜检查的工作量。与细胞学检查相比,p16 / mcm2对宫颈病变的识别更为敏感。

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