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Family history in the Finnish Prostate Cancer Screening Trial

机译:芬兰前列腺癌筛查试验的家族史

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Family history (FH) is one of the few known risk factors for prostate cancer (PC). There is also new evidence about mortality reduction in screening of PC with prostate-specific antigen (PSA). Therefore, we conducted a prospective study in the Finnish Prostate Cancer Screening Trial to evaluate the impact of FH on outcomes of PC screening. Of the 80,144 men enrolled, 31,866 men were randomized to the screening arm and were invited for screening with PSA test (cut-off 4 ng/ml) every 4 years. At the time of each invitation, FH of PC (FH) was assessed through a questionnaire. The analysis covered a follow-up of 12 years from randomization for all men with data on FH. Of the 23,702 (74.3%) invited men attending screening, 22,756 (96.0%) provided information of their FH. Altogether 1,723 (7.3%) men reported at least one first-degree relative diagnosed with PC and of them 235 (13.6%) were diagnosed with PC. Men with a first-degree FH had increased risk for PC (risk ratio (RR) 1.31, p<0.001) and the risk was especially elevated for interval cancer (RR 1.65, 95% CI 1.27-2.15). Risk for low-grade (Gleason 2-6) tumors was increased (RR 1.46, 95% CI 1.15-1.69), but it was decreased for Gleason 8-10 tumors (RR 0.48, 95% CI 0.25-0.95). PSA test performance (sensitivity and specificity) was slightly inferior for FH positives. No difference in PC mortality was observed in terms of FH. Our findings provide no support for selective PSA screening targeting men with FH of PC.
机译:家族病史(FH)是为数不多的已知前列腺癌(PC)危险因素之一。也有新证据表明,用前列腺特异性抗原(PSA)筛查PC会降低死亡率。因此,我们在芬兰前列腺癌筛查试验中进行了一项前瞻性研究,以评估FH对PC筛查结果的影响。在登记的80,144名男性中,有31,866名男性被随机分配到筛查组,并每4年接受一次PSA测试(临界值4 ng / ml)进行筛查。在每次邀请时,都会通过问卷调查来评估PC的FH(FH)。这项分析涵盖了从所有男性中随机抽取FH数据后12年的随访情况。在参加检查的23,702名(74.3%)受邀男子中,有22,756名(96.0%)提供了他们的FH信息。共有1,723名(7.3%)男性报告至少有一名一级亲戚被诊断为PC,其中235名(13.6%)被诊断为PC。患有一级FH的男性患PC的风险增加(风险比(RR)1.31,p <0.001),特别是间歇性癌症的风险较高(RR 1.65,95%CI 1.27-2.15)。低度(Gleason 2-6)肿瘤的风险增加(RR 1.46,95%CI 1.15-1.69),但对于Gleason 8-10肿瘤的风险降低(RR 0.48,95%CI 0.25-0.95)。 PSA检测性能(敏感性和特异性)略低于FH阳性。就FH而言,PC死亡率无差异。我们的发现不支持针对男性FH PC的选择性PSA筛查。

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