Department of Gynaecology and Obstetrics, Klinikum Wolfsburg, Wolfsburg, Germany.
Int J Cancer. 2014 Sep 15;135(6):1408-16. doi: 10.1002/ijc.28783. Epub 2014 Feb 27.
We evaluated compliance with human papillomavirus (HPV) testing and risk-adapted patient pathways and monitored changes in high-grade cervical disease during long-term follow-up. Women aged >30 years attending routine screening for cervical cancer were managed according to results from first-round screening tests (cytology and high-risk HPV; Hybrid Capture 2). Between February 2006 and January 2011, 19,795 of 19,947 women agreed to participate, of whom 4,067 proceeded to a second screening round 5 years after recruitment. Predefined endpoints were compliance, grade 3 cervical intraepithelial neoplasia or cancer (CIN3+), new HPV infection, HPV persistence and abnormal smears in round 2. A total of 765 of 19,795 women (3.9%) in round 1 and 41 of 4,067 (1.0%) in round 2 were referred for colposcopy. Compliance rates with colposcopy were 93.1 and 92.7%, respectively, while histological assessment was performed in 680 of 712 (95.5%) and 36 of 38 (94.7%), respectively. CIN3+ rates were 172 of 19,795 (0.87%; 95% confidence intervals: 0.7-1.0) in round 1 and 2 of 4,064 (0.05%; 95% confidence intervals: 0.006-0.2) in round 2; the difference was statistically significant (Fisher's exact test, p<0.001). After 5 years, the incidence of new HPV infection was 124 of 3,906 (3.2%) and HPV persistence was observed in 22 of 161 (13.7%). Locally organised HPV/cytology co-testing is feasible and acceptable to women. Risk-adapted management rapidly detected a high rate of prevalent CIN3+, while the subsequent long-term risk of new high-grade cervical disease was surprisingly low. It remains unclear if this phenomenon is explained by CIN3 mostly occurring early in life or by modifying the natural course of HPV infection with colposcopy and histological assessment.
我们评估了人乳头瘤病毒(HPV)检测和风险适应患者路径的依从性,并在长期随访中监测了高级别宫颈疾病的变化。接受常规宫颈癌筛查的 >30 岁女性根据首轮筛查检测(细胞学和高危型 HPV;杂交捕获 2)的结果进行管理。2006 年 2 月至 2011 年 1 月,在 19947 名同意参加的女性中,有 19795 名女性进入第二轮筛查,招募后 5 年进行第二轮筛查。预设终点为依从性、宫颈上皮内瘤变 3 级或癌症(CIN3+)、新的 HPV 感染、HPV 持续存在和第二轮筛查中异常涂片。首轮筛查中,共有 19795 名女性中的 765 名(3.9%)和第二轮筛查中 4067 名女性中的 41 名(1.0%)被转诊行阴道镜检查。阴道镜检查的依从率分别为 93.1%和 92.7%,而分别有 680 名(95.5%)和 36 名(94.7%)进行了组织学评估。首轮筛查中 CIN3+的发生率为 19795 名女性中的 172 名(0.87%;95%置信区间:0.7-1.0),第二轮筛查中 4064 名女性中的 2 名(0.05%;95%置信区间:0.006-0.2),差异具有统计学意义(Fisher 确切检验,p<0.001)。5 年后,新 HPV 感染的发生率为 3906 名女性中的 124 名(3.2%),HPV 持续存在率为 161 名女性中的 22 名(13.7%)。有组织地进行 HPV/细胞学联合检测对女性来说是可行和可接受的。风险适应管理迅速发现了高比例的普遍存在的 CIN3+,而随后新发生的高级别宫颈疾病的风险却出人意料地低。目前尚不清楚这种现象是由于 CIN3 主要发生在生命早期,还是由于阴道镜检查和组织学评估改变了 HPV 感染的自然病程。