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基于前列腺特异性抗原的风险分层前列腺癌筛查的终生获益和危害。

Lifetime Benefits and Harms of Prostate-Specific Antigen-Based Risk-Stratified Screening for Prostate Cancer.

机构信息

Department of Public Health, Erasmus MC, University Medical Center Rotterdam, Rotterdam, The Netherlands.

Division of Public Health Sciences, Fred Hutchinson Cancer Research Institute, Seattle, WA, USA.

出版信息

J Natl Cancer Inst. 2020 Oct 1;112(10):1013-1020. doi: 10.1093/jnci/djaa001.

Abstract

BACKGROUND

Studies conducted in Swedish populations have shown that men with lowest prostate-specific antigen (PSA) levels at ages 44-50 years and 60 years have very low risk of future distant metastasis or death from prostate cancer. This study investigates benefits and harms of screening strategies stratified by PSA levels.

METHODS

PSA levels and diagnosis patterns from two microsimulation models of prostate cancer progression, detection, and mortality were compared against results of the Malmö Preventive Project, which stored serum and tracked subsequent prostate cancer diagnoses for 25 years. The models predicted the harms (tests and overdiagnoses) and benefits (lives saved and life-years gained) of PSA-stratified screening strategies compared with biennial screening from age 45 years to age 69 years.

RESULTS

Compared with biennial screening for ages 45-69 years, lengthening screening intervals for men with PSA less than 1.0 ng/mL at age 45 years led to 46.8-47.0% fewer tests (range between models), 0.9-2.1% fewer overdiagnoses, and 3.1-3.8% fewer lives saved. Stopping screening when PSA was less than 1.0 ng/mL at age 60 years and older led to 12.8-16.0% fewer tests, 5.0-24.0% fewer overdiagnoses, and 5.0-13.1% fewer lives saved. Differences in model results can be partially explained by differences in assumptions about the link between PSA growth and the risk of disease progression.

CONCLUSION

Relative to a biennial screening strategy, PSA-stratified screening strategies investigated in this study substantially reduced the testing burden and modestly reduced overdiagnosis while preserving most lives saved. Further research is needed to clarify the link between PSA growth and disease progression.

摘要

背景

在瑞典人群中进行的研究表明,44-50 岁和 60 岁时前列腺特异性抗原(PSA)水平最低的男性患前列腺癌远处转移或死亡的风险极低。本研究调查了按 PSA 水平分层的筛查策略的获益和危害。

方法

比较了两种前列腺癌进展、检测和死亡率的微模拟模型的 PSA 水平和诊断模式,与马尔默预防项目的结果进行了比较,该项目储存了血清并跟踪了随后 25 年的前列腺癌诊断情况。这些模型预测了与从 45 岁到 69 岁每两年筛查一次相比,PSA 分层筛查策略的危害(检查和过度诊断)和益处(挽救生命和延长生命年)。

结果

与从 45 岁到 69 岁每两年筛查一次相比,对于 45 岁时 PSA 小于 1.0ng/mL 的男性,延长筛查间隔会导致检查减少 46.8-47.0%(模型之间的范围),过度诊断减少 0.9-2.1%,挽救生命减少 3.1-3.8%。当 60 岁及以上时 PSA 小于 1.0ng/mL 时停止筛查,会导致检查减少 12.8-16.0%,过度诊断减少 5.0-24.0%,挽救生命减少 5.0-13.1%。模型结果的差异部分可以用 PSA 增长与疾病进展风险之间的联系的假设差异来解释。

结论

与两年一次的筛查策略相比,本研究中研究的 PSA 分层筛查策略大大降低了检查负担,适度降低了过度诊断,同时保留了大部分挽救的生命。需要进一步研究来阐明 PSA 增长与疾病进展之间的联系。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5253/7566340/1efbe44f2588/djaa001f1.jpg

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