Hoeh Benedikt, Preisser Felix, Zattoni Fabio, Kretschmer Alexander, Westhofen Thilo, Olivier Jonathan, Soeterik Timo F W, van den Bergh Roderick C N, Mandel Philipp, Graefen Markus, Tilki Derya
Department of Urology, Medical Faculty Carl Gustav Carus, TU Dresden, Dresden, Germany.
Martini-Klinik Prostate Cancer Center, University Hospital Hamburg-Eppendorf, Hamburg, Germany.
Eur Urol Oncol. 2025 Apr;8(2):372-379. doi: 10.1016/j.euo.2024.08.008. Epub 2024 Sep 20.
Prostate-specific antigen (PSA) testing is used to follow up prostate cancer (PCa) patients treated with radical prostatectomy (RP). Research on PSA thresholds for identifying PCa patients with biochemical recurrence (BCR) who are at a higher risk of progression yielded inconclusive results. This study aims to investigate the risk of late BCR in PCa patients treated with RP and long postoperative (120 mo) undetectable PSA follow-up, and to identify prognostic factors for late BCR within this patient cohort.
PCa patients treated with curative RP (1992-2012) and free of BCR during the first 120 mo following RP were retrospectively identified within five European tertiary centers; BCR was defined as two consecutive PSA values of ≥0.2 ng/ml. Kaplan-Meier and Cox regression models tested for an association between BCR and patient or tumor characteristics.
The study cohort consisted of 4639 patients, of whom 243 (5.2%) developed BCR at a medium follow-up of 147 mo. Of those with BCR, 23 (9.5%) subsequently developed metastatic progression. In Kaplan-Meier models, BCR-free survival differed according to advanced tumor status. In multivariable Cox regression models, pT stage (pT3a: hazard ratio [HR]: 1.46; pT3b: HR: 2.42), pathological Gleason score (pGS 3 + 4: HR: 1.71; pGS ≥4 + 3: HR: 2.47), surgical margin (R1/Rx: HR: 1.72), and pNx stage (pNx: HR: 0.72) represented independent predictors for BCR (all p < 0.05). Conversely, age, PSA at diagnosis, and year of surgery failed to achieve independent predictor status for BCR.
Among PCa patients with an uneventful follow-up of at least 10 yr after RP, still one in 20 patients subsequently develop late BCR. Nevertheless, late BCR and subsequent progression to metastasis (0.3%) rates in patients with pT2 stage and pGS ≤3 + 4 were strikingly low, implicating that abandoning follow-up beyond an uneventful period of 10 yr is justifiable within this cohort of patients.
In this study, prostate cancer patients treated with a radical prostatectomy and at least 10 yr of uneventful prostate-specific antigen testing were identified within five European centers. Relying on these patients, the rate of subsequent late biochemical recurrence was calculated and risk factors were identified for biochemical recurrence following 10 yr of uneventful prostate-specific antigen testing.
前列腺特异性抗原(PSA)检测用于对接受根治性前列腺切除术(RP)的前列腺癌(PCa)患者进行随访。关于确定具有更高进展风险的生化复发(BCR)PCa患者的PSA阈值的研究结果尚无定论。本研究旨在调查接受RP治疗且术后长期(120个月)PSA检测未检出的PCa患者发生晚期BCR的风险,并确定该患者队列中晚期BCR的预后因素。
在五个欧洲三级中心回顾性确定1992年至2012年接受根治性RP治疗且术后前120个月内无BCR的PCa患者;BCR定义为连续两次PSA值≥0.2 ng/ml。采用Kaplan-Meier和Cox回归模型检验BCR与患者或肿瘤特征之间的关联。
研究队列包括4639例患者,其中243例(5.2%)在中位随访147个月时发生BCR。在发生BCR的患者中,23例(9.5%)随后发生转移进展。在Kaplan-Meier模型中,无BCR生存期因肿瘤进展状态而异。在多变量Cox回归模型中,pT分期(pT3a:风险比[HR]:1.46;pT3b:HR:2.42)、病理Gleason评分(pGS 3 + 4:HR:1.71;pGS≥4 + 3:HR:2.47)、手术切缘(R1/Rx:HR:1.72)和pNx分期(pNx:HR:0.72)是BCR的独立预测因素(均p < 0.05)。相反,年龄、诊断时的PSA和手术年份未能成为BCR的独立预测因素。
在RP术后至少10年随访无异常的PCa患者中,仍有二十分之一的患者随后发生晚期BCR。然而,pT2期和pGS≤3 + 4患者的晚期BCR及随后转移进展(0.3%)率极低,这意味着在该患者队列中,在10年无异常期后放弃随访是合理的。
在本研究中,在五个欧洲中心确定了接受根治性前列腺切除术且至少10年前列腺特异性抗原检测无异常的前列腺癌患者。基于这些患者,计算了随后晚期生化复发率,并确定了10年前列腺特异性抗原检测无异常后生化复发的风险因素。