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初次血清前列腺特异性抗原、前列腺特异性抗原进展与重复筛查时前列腺癌检测之间的关系。

Relationship among initial serum prostate specific antigen, prostate specific antigen progression and prostate cancer detection at repeat screening visits.

作者信息

Candas Bernard, Labrie Fernand, Gomez José Luis, Cusan Leonello, Chevrette Eric, Lévesque Jacques, Brousseau Ghyslain

机构信息

Department of Physiology and Anatomy, Laval University, Quebec City, Quebec, Canada.

出版信息

J Urol. 2006 Feb;175(2):510-6; discussion 516-7. doi: 10.1016/S0022-5347(05)00165-5.

Abstract

PURPOSE

We evaluated the probability of positive serum PSA (3 ng/ml or greater) and CaP detection at annual followup visits in men with negative initial PSA (less than 3 ng/ml) to optimize the re-screening schedule.

MATERIALS AND METHODS

Data on 5,387 men 45 to 80 years old with negative PSA and no CaP diagnosis at the first screening visit were obtained from the Laval University Prostate Cancer Screening Program database. Accelerated failure time regressions were fitted to time from baseline to positive PSA and to time from positive PSA to CaP detection. The models were combined to estimate the cumulative probability of positive PSA followed by CaP detection at re-screening.

RESULTS

The 5-year cumulative probability of detecting CaP at annual visits in men with baseline PSA up to 1.5 ng/ml remained below 0.8%, while it was 1.3%, 4.8% and 8.3% in men with PSA 1.5 to less than 2, 2 to less than 2.5 and 2.5 to less than 3 ng/ml, respectively. Time to positive PSA significantly decreased with increasing baseline PSA and age, while the time between positive PSA and CaP detection depended only on age. Men with PSA below 1.0 ng/ml could wait for 4 to 5 years before being re-tested, while men with PSA between 1.0 and 1.5 ng/ml should be screened every second year and men with PSA 1.5 ng/ml or greater should be screened every year.

CONCLUSIONS

The proposed retesting schedule using current PSA and age decreases the number of visits by 38.1%, while delaying the detection of only 2.4% of CaPs that would have been detected using annual PSA testing.

摘要

目的

我们评估了初始前列腺特异抗原(PSA)阴性(低于3 ng/ml)的男性在年度随访时血清PSA阳性(3 ng/ml或更高)及检测出前列腺癌(CaP)的概率,以优化重新筛查计划。

材料与方法

从拉瓦尔大学前列腺癌筛查项目数据库中获取了5387名年龄在45至80岁、首次筛查时PSA阴性且未诊断出CaP的男性的数据。对从基线到PSA阳性的时间以及从PSA阳性到CaP检测的时间进行加速失效时间回归分析。将这些模型结合起来估计重新筛查时PSA阳性随后检测出CaP的累积概率。

结果

基线PSA高达1.5 ng/ml的男性每年随访时检测出CaP的5年累积概率仍低于0.8%,而PSA为1.5至小于2 ng/ml、2至小于2.5 ng/ml和2.5至小于3 ng/ml的男性的该概率分别为1.3%、4.8%和8.3%。PSA阳性的时间随着基线PSA和年龄的增加而显著缩短,而PSA阳性与CaP检测之间的时间仅取决于年龄。PSA低于1.0 ng/ml的男性可以等待4至5年再进行重新检测,而PSA在1.0至1.5 ng/ml之间的男性应每两年筛查一次,PSA为1.5 ng/ml或更高的男性应每年筛查一次。

结论

使用当前PSA和年龄建议的重新检测计划使就诊次数减少了38.1%,同时仅延迟了2.4%原本通过每年PSA检测会被检测出的CaP的发现时间。

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