Department of Urology, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.
Department of Urology, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.
Eur Urol Oncol. 2024 Aug;7(4):713-720. doi: 10.1016/j.euo.2023.08.011. Epub 2023 Sep 9.
Previous research quantified the effect of prostate-specific antigen (PSA)-based prostate cancer (PCa) screening on quality-adjusted life years using 11-yr follow-up data from the European Randomized Study of Screening for Prostate Cancer (ERSPC) extrapolated by the Microsimulation Screening Analysis (MISCAN). ERSPC data now matured to 21 yr of follow-up.
To provide an overview of the effect of PSA-based screening on tumour characteristics and PCa treatment using long-term, detailed, empirical ERSPC data.
DESIGN, SETTING, AND PARTICIPANTS: Men were included from the ERSPC Rotterdam who were randomised to a PSA-based screening (S) or control (C) arm.
We assessed the effects of PSA-based screening on the number of PCa diagnoses, tumour characteristics, treatments, and cumulative incidence of disease progression. We also evaluated the changes in tumour characteristics and treatments over time for both study arms.
Among PCa patients in the S-arm, fewer patients were diagnosed with advanced tumour stages (T3/T4: 12% vs 23%; relative risk [RR] = 0.50; 95% confidence interval [CI] 0.44-0.57), less disease progression was observed, and less secondary treatment (30% vs 48%; RR = 0.61; 95% CI 0.57-0.66; p < 0.001) and less palliative treatment were needed (21% vs 55%; RR = 0.38; 95% CI 0.35-0.42) than among those in the C-arm. This was at the cost of overdiagnosis and increased local treatments (eg, radical prostatectomy: 32% vs 14%; RR = 2.18; 95% CI 1.92-2.48). Over time, the number of local treatments decreased, whereas expectant management strategies increased. The RRs of treatments were slightly different from those of the MISCAN.
After 21 yr of follow-up, empirical data of the ERSPC showed that PSA-based screening reduces advanced PCa stages, disease progression, and extensive treatments at the cost of more overdiagnosis and probably more overtreatment. Our data showed reduced local treatments and increased expectant management strategies over time.
Prostate-specific antigen-based screening reduces the number of invasive prostate cancer treatments needed, however, at the cost of more overdiagnosis and probably more overtreatment. Limiting these costs remains crucial to benefit optimally from prostate cancer screening.
先前的研究使用欧洲前列腺癌筛查随机研究(ERSPC)的 11 年随访数据,并通过微模拟筛查分析(MISCAN)外推,量化了前列腺特异性抗原(PSA)为基础的前列腺癌(PCa)筛查对质量调整生命年的影响。ERSPC 数据现在已经成熟到 21 年的随访。
使用长期、详细的 ERSPC 经验数据,提供基于 PSA 的筛查对肿瘤特征和 PCa 治疗的影响概述。
设计、设置和参与者:纳入来自 ERSPC 鹿特丹的随机分配至 PSA 为基础的筛查(S)或对照组(C)的男性。
我们评估了基于 PSA 的筛查对 PCa 诊断数量、肿瘤特征、治疗和疾病进展累积发生率的影响。我们还评估了两个研究臂的肿瘤特征和治疗随时间的变化。
在 S 臂的 PCa 患者中,较少的患者被诊断为晚期肿瘤阶段(T3/T4:12%比 23%;相对风险 [RR] 0.50;95%置信区间 [CI] 0.44-0.57),观察到较少的疾病进展,较少的二级治疗(30%比 48%;RR 0.61;95% CI 0.57-0.66;p<0.001)和较少的姑息治疗(21%比 55%;RR 0.38;95% CI 0.35-0.42)需要比 C 臂中的患者。这是基于过度诊断和增加局部治疗(例如,根治性前列腺切除术:32%比 14%;RR 2.18;95% CI 1.92-2.48)。随着时间的推移,局部治疗的数量减少,而期待管理策略增加。治疗的相对风险与 MISCAN 的相对风险略有不同。
在 21 年的随访后,ERSPC 的经验数据表明,基于 PSA 的筛查减少了高级 PCa 阶段、疾病进展和广泛的治疗,代价是更多的过度诊断和可能更多的过度治疗。我们的数据显示,随着时间的推移,局部治疗减少,期待管理策略增加。
基于前列腺特异性抗原的筛查减少了需要的侵袭性前列腺癌治疗数量,但代价是更多的过度诊断和可能更多的过度治疗。限制这些成本对于从前列腺癌筛查中获得最佳效益至关重要。