过度诊断
医学
前列腺癌
前列腺癌筛查
前列腺特异性抗原
前列腺
内科学
人口
置信区间
妇科
癌症
泌尿科
环境卫生
作者
Peter Albers,Agnė Krilavičiūtė,Petra Seibold,Maxime De Vrieze,Jale Lakes,Markus A. Kuczyk,Nina N. Harke,Jürgen Debus,Christoph A. Fink,Jürgen E. Gschwend,Kathleen Herkommer,V A Soehne,Axel Benner,Glen Kristiansen,Boris Hadaschik,Christian Arsov,Gerald Antoch,Lars Schimmöller,Frederik L. Giesel,Marcus R. Makowski
标识
DOI:10.1016/j.euo.2025.06.007
摘要
In general, low-risk and favorable intermediate-risk prostate cancers (PCs; International Society of Urological Pathology grade group [GG] 1 and GG 2) are slow-growing cancers with low metastatic potential. Active surveillance is recommended for GG 1 PC and can be recommended for GG 2 PC in the absence of adverse pathological parameters. Therefore, the question arises as to when low-grade PC should be detected in a screening setting. We conducted an analysis of the group with intermediate prostate-specific antigen (PSA) risk (1.5-2.99 ng/ml) from the PROBASE screening trial for young men (starting age 45 yr) and evaluated 159 biopsies performed for confirmed PSA ≥3 ng/ml in the first two biennial screening rounds. Of these biopsies, 37% were positive, with 78% (46/59) showing GG 1 or GG 2 disease. Only 0.8% of men with intermediate risk (13 of 1661 men screened) had GG 3-5 PC and would have experienced a delay in diagnosis of between 1 and 3 yr if screening were performed at 5-yr intervals. These results suggest that the screening interval could be extended from 2 yr to 5 yr for men aged 45 yr at intermediate risk, similar to the interval for men at low risk (PSA <1.5 ng/ml). This would reduce unnecessary testing and overdiagnosis in nearly 10% of the screening population aged 45 yr.
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