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Prediction of significant prostate cancer diagnosed 20 to 30 years later with a single measure of prostate-specific antigen at or before age 50.

机译:在20到30年后使用50岁或之前的前列腺特异性抗原的单一指标诊断诊断出的重大前列腺癌。

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摘要

BACKGROUND: We previously reported that a single prostate-specific antigen (PSA) measured at ages 44-50 was highly predictive of subsequent prostate cancer diagnosis in an unscreened population. Here we report an additional 7 years of follow-up. This provides replication using an independent data set and allows estimates of the association between early PSA and subsequent advanced cancer (clinical stage ≥T3 or metastases at diagnosis). METHODS: Blood was collected from 21,277 men in a Swedish city (74% participation rate) during 1974-1986 at ages 33-50. Through 2006, prostate cancer was diagnosed in 1408 participants; we measured PSA in archived plasma for 1312 of these cases (93%) and for 3728 controls. RESULTS: At a median follow-up of 23 years, baseline PSA was strongly associated with subsequent prostate cancer (area under the curve, 0.72; 95% CI, 0.70-0.74; for advanced cancer, 0.75; 95% CI, 0.72-0.78). Associations between PSA and prostate cancer were virtually identical for the initial and replication data sets, with 81% of advanced cases (95% CI, 77%-86%) found in men with PSA above the median (0.63 ng/mL at ages 44-50). CONCLUSIONS: A single PSA at or before age 50 predicts advanced prostate cancer diagnosed up to 30 years later. Use of early PSA to stratify risk would allow a large group of low-risk men to be screened less often but increase frequency of testing on a more limited number of high-risk men. This is likely to improve the ratio of benefit to harm for screening.
机译:背景:我们先前报道,在未筛查人群中,在44至50岁之间测量的单个前列腺特异性抗原(PSA)可以高度预测随后的前列腺癌诊断。在这里,我们报告了另外7年的随访。这样可以使用独立的数据集进行复制,并可以估算早期PSA与随后的晚期癌症(临床分期≥T3或诊断时转移)之间的关联。方法:在1974-1986年期间,从33277岁的瑞典城市21277名男性(参与率74%)中抽取血液。到2006年,共有1408名参与者被诊断出患有前列腺癌。我们测量了1312例此类病例(93%)和3728例对照的血浆中PSA。结果:在平均23年的随访中,基线PSA与随后的前列腺癌密切相关(曲线下面积0.72; 95%CI 0.70-0.74;晚期癌症0.75; 95%CI 0.72-0.78 )。 PSA和前列腺癌之间的关联在初始数据和复制数据集上几乎相同,其中PSA高于中位数(44岁时为0.63 ng / mL)的男性中有81%的晚期病例(95%CI,77%-86%) -50)。结论:50岁或50岁之前的单个PSA可预测到30年后诊断为晚期前列腺癌。使用早期PSA进行风险分层可减少对大量低风险男性的筛查,但增加了对数量有限的高风险男性进行检测的频率。这可能会提高筛查的利弊比率。

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