Peter Albers, Agne Krilaviciute, Petra Seibold, Maxime de Vrieze, Jale Lakes, Markus A Kuczyk, Nina N Harke, Jürgen Debus, Christoph A Grott, Jürgen E Gschwend, Kathleen Herkommer, Victoria A Soehne, Axel Benner, Glen Kristiansen, Boris Hadaschik, Christian Arsov, Gerald Antoch, Lars Schimmöller, Frederik L Giesel, Marcus R Makowski, Frank Wacker, Heinz-Peter Schlemmer, Rudolf Kaaks, Nikolaus Becker
{"title":"在年轻男性的筛查项目中,我们需要早期发现2级前列腺癌吗?PROBASE筛选试验结果。","authors":"Peter Albers, Agne Krilaviciute, Petra Seibold, Maxime de Vrieze, Jale Lakes, Markus A Kuczyk, Nina N Harke, Jürgen Debus, Christoph A Grott, Jürgen E Gschwend, Kathleen Herkommer, Victoria A Soehne, Axel Benner, Glen Kristiansen, Boris Hadaschik, Christian Arsov, Gerald Antoch, Lars Schimmöller, Frederik L Giesel, Marcus R Makowski, Frank Wacker, Heinz-Peter Schlemmer, Rudolf Kaaks, Nikolaus Becker","doi":"10.1016/j.euo.2025.06.007","DOIUrl":null,"url":null,"abstract":"<p><p>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.</p>","PeriodicalId":12256,"journal":{"name":"European urology oncology","volume":" ","pages":""},"PeriodicalIF":8.3000,"publicationDate":"2025-07-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Do We Need Early Detection of Grade Group 2 Prostate Cancer in a Screening Program for Young Men? Results from the PROBASE Screening Trial.\",\"authors\":\"Peter Albers, Agne Krilaviciute, Petra Seibold, Maxime de Vrieze, Jale Lakes, Markus A Kuczyk, Nina N Harke, Jürgen Debus, Christoph A Grott, Jürgen E Gschwend, Kathleen Herkommer, Victoria A Soehne, Axel Benner, Glen Kristiansen, Boris Hadaschik, Christian Arsov, Gerald Antoch, Lars Schimmöller, Frederik L Giesel, Marcus R Makowski, Frank Wacker, Heinz-Peter Schlemmer, Rudolf Kaaks, Nikolaus Becker\",\"doi\":\"10.1016/j.euo.2025.06.007\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>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). 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Do We Need Early Detection of Grade Group 2 Prostate Cancer in a Screening Program for Young Men? Results from the PROBASE Screening Trial.
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.
期刊介绍:
Journal Name: European Urology Oncology
Affiliation: Official Journal of the European Association of Urology
Focus:
First official publication of the EAU fully devoted to the study of genitourinary malignancies
Aims to deliver high-quality research
Content:
Includes original articles, opinion piece editorials, and invited reviews
Covers clinical, basic, and translational research
Publication Frequency: Six times a year in electronic format