Paschen Ulrike, Sturtz Sibylle, Fleer Daniel, Lampert Ulrike, Skoetz Nicole, Dahm Philipp
Institut für Qualität und Wirtschaftlichkeit im Gesundheitswesen (IQWiG), Köln, Germany.
Department I of Internal Medicine, Faculty of Medicine and University Hospital Cologne, Center for Integrated Oncology Aachen Bonn Cologne Dusseldorf, Evidence-Based Oncology, University of Cologne, Cologne, Germany.
BJU Int. 2022 Mar;129(3):280-289. doi: 10.1111/bju.15444. Epub 2021 Jul 7.
Prostate-specific antigen (PSA) testing increases prostate cancer diagnoses and reduces long-term disease-specific mortality, but also results in overdiagnoses and treatment-related harms.
To systematically assess the benefits and harms of population-based PSA screening and the potential net benefit to inform health policy decision-makers in Germany.
We performed a protocol-guided comprehensive literature search according to the Preferred Reporting Items for Systematic Reviews and Meta-analyses (PRISMA) statement. All steps were performed by one or two investigators; any discrepancies were resolved by consensus. To allow subgroup analyses for identifying the optimal screening parameters, the eight national trials conducted under the umbrella of the European Randomised study of Screening for Prostate Cancer (ERSPC) were included as individual trials.
We included a total 11 randomised controlled trials (RCTs) with a total of 416 000 study participants. For all-cause mortality, we found neither benefit nor harm. PSA screening was associated with a reduced risk of both prostate cancer mortality and the development of metastases. For the outcomes of health-related quality of life, adverse effects and the consequences of false-negative screening results there was no difference; however, this was due to the lack of eligible RCT data. Finally, PSA screening was associated with large numbers of overdiagnoses with adverse downstream consequences of unnecessary treatment (e.g. incontinence, erectile dysfunction) and large numbers of false-positive PSA tests leading to biopsies associated with a small but not negligible risk of complications. Limitations of this assessment include the clinical heterogeneity and methodological limitations of the underlying studies.
The benefits of PSA-based prostate cancer screening do not outweigh its harms. We failed to identify eligible screening studies of newer biomarkers, PSA derivatives or modern imaging modalities, which may alter the balance of benefit to harm.
In the present study, we reviewed the evidence on the PSA blood test to screen men without symptoms for prostate cancer. We found that the small benefits experienced by some men do not outweigh the harms to many more men.
前列腺特异性抗原(PSA)检测增加了前列腺癌的诊断率并降低了长期疾病特异性死亡率,但也导致了过度诊断和与治疗相关的危害。
系统评估基于人群的PSA筛查的益处和危害以及潜在的净效益,以为德国的卫生政策决策者提供参考。
我们根据系统评价和Meta分析的首选报告项目(PRISMA)声明进行了方案指导的全面文献检索。所有步骤均由一两名研究人员执行;任何差异均通过协商一致解决。为了进行亚组分析以确定最佳筛查参数,在欧洲前列腺癌筛查随机研究(ERSPC)框架下进行的八项国家试验被作为独立试验纳入。
我们总共纳入了11项随机对照试验(RCT),共有416000名研究参与者。对于全因死亡率,我们未发现益处或危害。PSA筛查与前列腺癌死亡率降低和转移发生风险降低相关。对于健康相关生活质量、不良反应和假阴性筛查结果的后果等结局,没有差异;然而,这是由于缺乏符合条件的RCT数据。最后,PSA筛查与大量过度诊断相关,这些过度诊断会带来不必要治疗的不良下游后果(如尿失禁、勃起功能障碍),以及大量导致活检的PSA假阳性检测,活检伴有虽小但不可忽视的并发症风险。该评估的局限性包括基础研究的临床异质性和方法学局限性。
基于PSA的前列腺癌筛查的益处并不大于其危害。我们未能找到关于更新的生物标志物、PSA衍生物或现代成像方式的符合条件的筛查研究,这些可能会改变利弊平衡。
在本研究中,我们回顾了关于PSA血液检测筛查无症状男性前列腺癌的证据。我们发现,一些男性获得的微小益处并不大于更多男性所遭受的危害。