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50 岁时或之前单次前列腺特异性抗原检测预测 20 至 30 年后诊断的显著前列腺癌。

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

机构信息

Department of Clinical Laboratories, Memorial Sloan-Kettering Cancer Center, New York, New York, USA.

出版信息

Cancer. 2011 Mar 15;117(6):1210-9. doi: 10.1002/cncr.25568. Epub 2010 Oct 19.

DOI:10.1002/cncr.25568
PMID:20960520
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3412541/
Abstract

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.

摘要

背景

我们之前报道过,在未接受筛查的人群中,44-50 岁时单次测量的前列腺特异性抗原(PSA)高度预测随后的前列腺癌诊断。在此,我们报告了另外 7 年的随访结果。这是使用独立数据集进行的复制研究,并且可以评估早期 PSA 与随后的高级别癌症(临床分期≥T3 或诊断时转移)之间的关联。

方法

1974 年至 1986 年间,在瑞典的一个城市采集了 21277 名男性的血液(参与率为 74%),年龄在 33-50 岁之间。截至 2006 年,共有 1408 名参与者被诊断为前列腺癌;我们对其中 1312 例(93%)和 3728 名对照者的存档血浆进行了 PSA 测量。

结果

中位随访 23 年,基线 PSA 与随后的前列腺癌显著相关(曲线下面积为 0.72;95%CI,0.70-0.74;对于高级别癌症,为 0.75;95%CI,0.72-0.78)。初始和复制数据集之间 PSA 与前列腺癌的相关性几乎相同,81%的高级别病例(95%CI,77%-86%)出现在 PSA 高于中位数(44-50 岁时为 0.63ng/ml)的男性中。

结论

50 岁或之前的单次 PSA 可预测 30 年后诊断的高级别前列腺癌。使用早期 PSA 进行风险分层可以使大量低危男性减少筛查次数,但增加对少数高危男性的检测频率。这可能会提高筛查的获益与危害比。

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