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首页> 外文期刊>The Lancet >Screening and prostate cancer mortality: Results of the European Randomised Study of Screening for Prostate Cancer (ERSPC) at 13 years of follow-up
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Screening and prostate cancer mortality: Results of the European Randomised Study of Screening for Prostate Cancer (ERSPC) at 13 years of follow-up

机译:筛查和前列腺癌死亡率:随访13年的欧洲前列腺癌筛查随机研究(ERSPC)的结果

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摘要

Background The European Randomised study of Screening for Prostate Cancer (ERSPC) has shown significant reductions in prostate cancer mortality after 9 years and 11 years of follow-up, but screening is controversial because of adverse events such as overdiagnosis. We provide updated results of mortality from prostate cancer with follow-up to 2010, with analyses truncated at 9, 11, and 13 years.Methods ERSPC is a multicentre, randomised trial with a predefined centralised database, analysis plan, and core age group (55-69 years), which assesses prostate-specific antigen (PSA) testing in eight European countries. Eligible men aged 50-74 years were identified from population registries and randomly assigned by computer generated random numbers to screening or no intervention (control). Investigators were masked to group allocation. The primary outcome was prostate cancer mortality in the core age group. Analysis was by intention to treat. We did a secondary analysis that corrected for selection bias due to non-participation. Only incidence and no mortality data at 9 years' follow-up are reported for the French centres. This study is registered with Current Controlled Trials, number ISRCTN49127736.Findings With data truncated at 13 years of follow-up, 7408 prostate cancer cases were diagnosed in the intervention group and 6107 cases in the control group. The rate ratio of prostate cancer incidence between the intervention and control groups was 1·91 (95% CI 1·83-1·99) after 9 years (1·64 [1·58-1·69] including France), 1·66 (1·60-1·73) after 11 years, and 1·57 (1·51-1·62) after 13 years. The rate ratio of prostate cancer mortality was 0·85 (0·70-1·03) after 9 years, 0·78 (0·66-0·91) after 11 years, and 0·79 (0·69-0·91) at 13 years. The absolute risk reduction of death from prostate cancer at 13 years was 0·11 per 1000 person-years or 1·28 per 1000 men randomised, which is equivalent to one prostate cancer death averted per 781 (95% CI 490-1929) men invited for screening or one per 27 (17-66) additional prostate cancer detected. After adjustment for non-participation, the rate ratio of prostate cancer mortality in men screened was 0·73 (95% CI 0·61-0·88).Interpretation In this update the ERSPC confirms a substantial reduction in prostate cancer mortality attributable to testing of PSA, with a substantially increased absolute effect at 13 years compared with findings after 9 and 11 years. Despite our findings, further quantification of harms and their reduction are still considered a prerequisite for the introduction of populated-based screening.Funding Each centre had its own funding responsibility.
机译:背景技术一项欧洲前列腺癌筛查随机研究(ERSPC)显示,在随访9年和11年后,前列腺癌的死亡率显着降低,但由于不良事件(如过度诊断),筛查存在争议。我们提供截至2010年的前列腺癌死亡率的最新结果,并在9、11和13年时进行分析。方法ERSPC是一项多中心,随机试验,具有预定义的集中式数据库,分析计划和核心年龄组( 55-69岁),该评估评估了八个欧洲国家/地区的前列腺特异性抗原(PSA)测试。从人口登记处确定年龄在50-74岁之间的合格男性,并通过计算机生成的随机数对其进行随机分配,以进行筛查或不进行干预(对照)。调查人员被掩盖到小组分配中。主要结果是核心年龄组的前列腺癌死亡率。分析是按意向进行的。我们进行了二次分析,以纠正由于未参与而导致的选择偏见。据报道,法国各中心在9年的随访中只有发病率,没有死亡率数据。该研究已在电流对照试验中注册,编号ISRCTN49127736。调查结果在随访13年后被截断,干预组诊断为7408例前列腺癌,对照组诊断为6107例。 9年后(包括法国在内的1·64 [1·58-1·69]),干预组和对照组之间前列腺癌的发生率比率为1·91(95%CI 1·83-1·99),1 11年后·66(1·60-1·73),13年后1·57(1·51-1·62)。 9年后前列腺癌死亡率的比率为0·85(0·70-1·03),11年后0·78(0·66-0·91)和0·79(0·69-0) ·91)在13岁。 13岁时前列腺癌死亡的绝对危险度降低为每1000人年0·11或随机分配的每1000名男性1·28,这相当于每781名男性(95%CI 490-1929)避免了一名前列腺癌死亡邀请进行筛查或每27(17-66)个额外的前列腺癌中检出一个。调整非参与性后,筛查的男性前列腺癌死亡率的比率为0·73(95%CI 0·61-0·88)。解释在此更新中,ERSPC确认可归因于前列腺癌的死亡率显着降低对PSA进行测试,与9和11年后的结果相比,在13年时的绝对效果大大提高。尽管有我们的发现,对危害的进一步量化和减少仍然被认为是引入基于人群的筛查的前提条件。资金每个中心都有自己的资金责任。

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