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Randomised prostate cancer screening trial: 20 year follow-up

机译:随机前列腺癌筛查试验:20年随访

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摘要

>Objective To assess whether screening for prostate cancer reduces prostate cancer specific mortality.>Design Population based randomised controlled trial.>Setting Department of Urology, Norrköping, and the South-East Region Prostate Cancer Register.>Participants All men aged 50-69 in the city of Norrköping, Sweden, identified in 1987 in the National Population Register (n=9026).>Intervention From the study population, 1494 men were randomly allocated to be screened by including every sixth man from a list of dates of birth. These men were invited to be screened every third year from 1987 to 1996. On the first two occasions screening was done by digital rectal examination only. From 1993, this was combined with prostate specific antigen testing, with 4 µg/L as cut off. On the fourth occasion (1996), only men aged 69 or under at the time of the investigation were invited.>Main outcome measures Data on tumour stage, grade, and treatment from the South East Region Prostate Cancer Register. Prostate cancer specific mortality up to 31 December 2008.>Results In the four screenings from 1987 to 1996 attendance was 1161/1492 (78%), 957/1363 (70%), 895/1210 (74%), and 446/606 (74%), respectively. There were 85 cases (5.7%) of prostate cancer diagnosed in the screened group and 292 (3.9%) in the control group. The risk ratio for death from prostate cancer in the screening group was 1.16 (95% confidence interval 0.78 to 1.73). In a Cox proportional hazard analysis comparing prostate cancer specific survival in the control group with that in the screened group, the hazard ratio for death from prostate cancer was 1.23 (0.94 to 1.62; P=0.13). After adjustment for age at start of the study, the hazard ratio was 1.58 (1.06 to 2.36; P=0.024).>Conclusions After 20 years of follow-up the rate of death from prostate cancer did not differ significantly between men in the screening group and those in the control group.>Trial registration Current Controlled Trials, ISRCTN06342431.
机译:>目的,以评估筛查前列腺癌是否可以降低前列腺癌的特异性死亡率。>设计基于人群的随机对照试验。>设置,诺尔雪平泌尿外科和>参与者,于1987年在国家人口登记簿(n = 9026)中确定的瑞典Norrköping市所有50-69岁的男性。>干预< / strong>从研究人群中随机分配1494名男性进行筛查,方法是从出生日期列表中将每6名男性包括在内。从1987年至1996年,每三年对这些人进行检查。在前两次检查中,仅通过数字直肠检查进行检查。从1993年开始,将其与前列腺特异性抗原检测结合使用,以4 µg / L的临界值截止。第四次(1996年)只邀请了调查时年龄在69岁以下的男性。>主要结果指标来自东南地区前列腺癌登记处的肿瘤分期,等级和治疗数据。截至2008年12月31日的前列腺癌特异性死亡率。>结果在1987年至1996年的四次筛查中,就诊人数分别为1161/1492(78%),957/1363(70%),895/1210(74%) )和446/606(74%)。筛查组确诊为前列腺癌85例(5.7%),对照组为292例(3.9%)。筛查组死于前列腺癌的风险比为1.16(95%置信区间为0.78至1.73)。在Cox比例风险分析中,比较对照组和筛查组的前列腺癌特异性存活率,死于前列腺癌的风险比为1.23(0.94至1.62; P = 0.13)。在研究开始时调整年龄后,危险比为1.58(1.06至2.36; P = 0.024)。>结论随访20年后,前列腺癌的死亡率没有差异>试验注册当前对照试验,ISRCTN06342431。

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