Arvendell Markus, Björnebo Lars, Eklund Martin, Giovanni Falagario Ugo, Chandra Engel Jan, Akre Olof, Grönberg Henrik, Nordström Tobias, Lantz Anna
Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.
Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.
Eur Urol Open Sci. 2024 Mar 4;62:61-67. doi: 10.1016/j.euros.2024.02.011. eCollection 2024 Apr.
Prostate cancer (PC) is the fifth leading cause of cancer-related mortality in men worldwide. Opportunistic testing with prostate-specific antigen (PSA) has limited impact on PC mortality. Our objective was to assess prediagnostic PSA testing patterns and clinical characteristics at diagnosis in men with lethal PC.
We conducted a population-based observational study of all men dying from PC in Stockholm County, Sweden, from 2015 to 2019. Data were retrieved from the National Prostate Cancer Register and the Stockholm PSA and Biopsy Register. If the first PSA was registered within 1 yr before diagnosis, men were categorised as PSA naïve. If an elevated PSA level was registered >1 yr before diagnosis without leading to prostate biopsy or repeating PSA within 1 yr, men were categorised as having delayed diagnosis. If a normal PSA level was registered within 5 yr before diagnosis, followed by an elevated PSA level that resulted in PC diagnosis within 1 yr, men were categorised as PSA tested. Clinical characteristics at diagnosis were stratified with D'Amico risk group classification.
Among 1473 men dying from PC, PSA test history was available for 995. Of these men, 60% ( = 592) were PSA naïve, 25% ( = 250) received delayed diagnosis, and 15% ( = 153) were PSA tested. After examining all 1473 men, 25% ( = 350) were diagnosed with low- or intermediate-risk cancer, 48% ( = 687) with high-risk cancer, and 27% ( = 385) with metastatic disease. Limitations include the retrospective design.
Many men with lethal PC lacked PSA testing before diagnosis or had been tested without subsequent follow-up. Nearly half of the study population was diagnosed with high-risk cancer and almost one-third with metastatic disease. These findings suggest further evaluation of the current opportunistic PSA testing approach.
Data from a population-based observational study of men dying from prostate cancer showed that many of them did not undergo either prostate-specific antigen (PSA) testing before diagnosis or subsequent follow-up if tested. These findings implicate deficiencies in the current opportunistic PSA testing approach.
前列腺癌(PC)是全球男性癌症相关死亡的第五大主要原因。采用前列腺特异性抗原(PSA)进行机会性检测对前列腺癌死亡率的影响有限。我们的目的是评估致命性前列腺癌男性患者诊断前的PSA检测模式及诊断时的临床特征。
我们对2015年至2019年瑞典斯德哥尔摩县所有死于前列腺癌的男性进行了一项基于人群的观察性研究。数据取自国家前列腺癌登记处以及斯德哥尔摩PSA和活检登记处。如果首次PSA检测是在诊断前1年内登记的,则将男性患者归类为未进行过PSA检测。如果在诊断前1年以上记录到PSA水平升高,但未导致前列腺活检或在1年内重复进行PSA检测,则将男性患者归类为诊断延迟。如果在诊断前5年内记录到PSA水平正常,随后在1年内因PSA水平升高而被诊断为前列腺癌,则将男性患者归类为进行过PSA检测。诊断时的临床特征根据达米科风险组分类进行分层。
在1473例死于前列腺癌的男性中,有995例有PSA检测史。在这些男性中,60%(n = 592)未进行过PSA检测,25%(n = 250)诊断延迟,15%(n = 153)进行过PSA检测。在检查了所有这1473例男性后,25%(n = 350)被诊断为低风险或中风险癌症,48%(n = 687)为高风险癌症,27%(n = 385)为转移性疾病。局限性包括研究设计为回顾性。
许多致命性前列腺癌男性患者在诊断前未进行PSA检测,或检测后未进行后续随访。近一半的研究人群被诊断为高风险癌症,近三分之一为转移性疾病。这些发现提示应对当前的机会性PSA检测方法进行进一步评估。
一项基于人群的前列腺癌死亡男性观察性研究的数据显示,其中许多人在诊断前未进行前列腺特异性抗原(PSA)检测,或者检测后未进行后续随访。这些发现表明当前的机会性PSA检测方法存在缺陷。