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Rate of cervical cancer severe intraepithelial neoplasia and adenocarcinoma in situ in primary HPV DNA screening with cytology triage: randomised study within organised screening programme

机译:通过细胞学分诊进行的初次HPV DNA筛查中子宫颈癌严重上皮内瘤变和原位腺癌的发生率:有组织筛查计划中的随机研究

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摘要

>Objective To assess the performance and impact of primary human papillomavirus (HPV) DNA screening with cytology triage compared with conventional cytology on cervical cancer and severe pre-cancerous lesions.>Design Randomised trial.>Setting Population based screening programme for cervical cancer in southern Finland in 2003-5.>Participants 58 076 women, aged 30-60, invited to the routine population based screening programme for cervical cancer.>Interventions Primary HPV DNA test (hybrid capture II) with cytology triage if the result was positive or conventional cytological screening (reference).>Main outcome measures Rate of cervical cancer, cervical intraepithelial neoplasia (CIN) grade III, and adenocarcinoma in situ (as a composite outcome referred to as CIN III+) during 2003-7 through record linkage between files from the screening registry and the national cancer registry.>Results In the HPV and conventional arms there were 95 600 and 95 700 woman years of follow-up and 76 and 53 cases of CIN III+, respectively (of which six and eight were cervical cancers). The relative rate of CIN III+ in the HPV arm versus the conventional arm was 1.44 (95% confidence interval 1.01 to 2.05) among all women invited for screening and 1.77 (1.16 to 2.74) among those who attended. Among women with a normal or negative test result, the relative rate of subsequent CIN III+ was 0.28 (0.04 to 1.17). The rate of cervical cancer between arms was 0.75 (0.25 to 2.16) among women invited for screening and 1.98 (0.52 to 9.38) among those who attended.>Conclusions When incorporated into a well established organised screening programme, primary HPV screening with cytology triage was more sensitive than conventional cytology in detecting CIN III+ lesions. The number of cases of cervical cancer was small, but considering the high probability of progression of CIN III the findings are of importance regarding cancer prevention.>Trial registration Current Controlled Trials ISRCTN23885553.
机译:>目的旨在通过细胞学分诊与常规细胞学比较评估原发性人乳头瘤病毒(HPV)DNA筛查对宫颈癌和严重癌前病变的性能和影响。>设计随机试验> Setting (设置)芬兰南部地区2003年基于子宫颈癌的人群筛查计划。>参与者 58 076名30-60岁的女性,被邀请参加常规的基于人群的宫颈癌筛查计划>干预:如果结果为阳性或进行常规细胞学筛查,则进行细胞学分流的原发性HPV DNA测试(杂交捕获II)(参考)。>主要结局指标 ,登记册和国家癌症登记册之间的记录联系,从而在2003-7年期间检测到了宫颈癌,III型宫颈上皮内瘤变(CIN)和原位腺癌(复合结果称为CIN III +)。> Resu 在HPV和常规组中,女性随访时间为95 600和95 700岁,分别为76和53例CIN III +(其中6和8例是宫颈癌)。在所有接受筛查的女性中,HPV组与常规组中CIN III +的相对比率为1.44(95%置信区间1.01至2.05),而参加检查的女性为1.77(1.16至2.74)。在测试结果正常或阴性的女性中,其后CIN III +的相对发生率为0.28(0.04至1.17)。受邀筛查的妇女手臂间子宫颈癌的发生率为0.75(0.25至2.16),参加检查的妇女则为1.98(0.52至9.38)。>结论用细胞学分类进行HPV筛查比常规细胞学对检测CIN III +病变更为敏感。子宫颈癌病例虽少,但考虑到CIN III进展的可能性很高,因此这一发现对预防癌症具有重要意义。>试验注册现行对照试验ISRCTN23885553。

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