有下尿路症状或进行机会性筛查的男性的前列腺癌诊断路径:意大利泌尿外科学会(SIU)立场文件。

IF 4.9 2区 医学 Q1 UROLOGY & NEPHROLOGY Minerva Urology and Nephrology Pub Date : 2024-10-01 DOI:10.23736/S2724-6051.24.06118-4
Vincenzo Ficarra, Riccardo Bartoletti, Marco Borghesi, Cosimo DE Nunzio, Ugo G Falagario, Giorgio Gandaglia, Gianluca Giannarini, Andrea Minervini, Vincenzo Mirone, Francesco Porpiglia, Bernardo Rocco, Andrea Salonia, Paolo Verze, Giuseppe Carrieri
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引用次数: 0

摘要

背景:自愿性 PCa 筛查经常会导致不必要的诊断性检查使用过多,并增加检出不典型 PCa 的风险,使各国医疗系统无法承担费用。在这种情况下,意大利泌尿外科学会(Società Italiana di Urologia, SIU)提出了一个有条理的流程图,指导医生提高对重大 PCa 的早期诊断率,避免不必要的诊断检查和前列腺活检:方法:根据现有证据和有关 PCa 的国际指南(即欧洲泌尿外科协会 (EAU)、美国泌尿外科协会 (AUA) 和美国国立综合癌症网络 (NCCN)),由意大利泌尿外科学会 (SIU, Società Italiana di Urologia) 选定的泌尿外科专家组成的专家小组提出了一些适应症,以便根据临床实践中主要使用的诊断测试制定逐步诊断路径。最终文件提交给六位泌尿科专家进行外部修订和批准。此外,还与患者权益组织分享了最终文件:对于 PSA 值升高(>3 纳克/毫升)的自愿男性和无症状患者,专家小组强烈反对在没有尿培养证实尿路感染的情况下使用抗生素。DRE 仍是泌尿科体检的关键部分,有助于泌尿科医生正确解读 PSA 升高,并在出现可疑 PCa 时优先执行多参数磁共振成像 (mpMRI)。对于 mpMRI 呈阴性、临床怀疑 PSA 较低的男性(PSA 密度< 0.20 ng/mL/cc、DRE 结果阴性、无家族史),可对其进行进一步监测。对于 mpMRI 阴性且 PCa 风险较高的男性(家族史、可疑 DRE、PSAD>0.20 ng/mL/cc 或 PSA>20 ng/mL),应考虑进行系统性前列腺活检。PI-RADS 4-5 级病变是前列腺活检的强烈指征,而 PI-RADS 3 级病变则应根据 PSAD 值进一步分层,并在 PSAD 超过 0.20 时进行前列腺活检。应大力考虑对放射医师和前列腺 mpMRI 中心进行认证、鉴定和质量审核。还应在诊断路径中评估 MRI 检查的可及性和/或候诊名单。专家组建议将经会阴或经直肠靶向加系统活检作为标准治疗:科学协会必须支持使用共享诊断路径,以提高重大 PCa 的早期发现率,减少晚期 PCa 的延迟诊断。此外,共享诊断路径还能减少抗生素的错误使用、不必要的实验室和放射检查以及前列腺活检的次数。
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Prostate cancer diagnostic pathway in men with lower urinary tract symptoms or performing opportunistic screening: The Italian Society of Urology (SIU) position paper.

Background: Voluntary PCa screening frequently results in excessive use of unnecessary diagnostic tests and an increasing risk of detection of indolent PCa and unaffordable costs for the various national health systems. In this scenario, the Italian Society of Urology (Società Italiana di Urologia, SIU) proposes an organized flow chart guiding physicians to improve early diagnosis of significant PCa avoiding unnecessary diagnostic tests and prostate biopsy.

Methods: According to available evidence and international guidelines [i.e., European Association of Urology (EAU), American Association of Urology (AUA) and National Comprehensive Cancer Network (NCCN)] on PCa, a Panel of expert urologists selected by Italian Society of Urology (SIU, Società Italiana di Urologia) proposed some indications to develop a stepwise diagnostic pathway based on the diagnostic tests mainly used in the clinical practice. The final document was submitted to six expert urologists for external revision and approval. Moreover, the final document was shared with patient advocacy groups.

Results: In voluntary men and symptomatic patients with elevated PSA value (>3 ng/mL), the Panel strongly discourage the use of antibiotic agents in absence of urinary tract infection confirmed by urine culture. DRE remains a key part of the urologic physical examination helping urologists to correctly interpret PSA elevation and prioritizing the execution of multiparametric Magnetic Resonance Imaging (mpMRI) in presence of suspicious PCa. Men with negative mpMRI and low clinical suspicion of PSA (PSA density < 0.20 ng/mL/cc, negative DRE findings, no family history) can be further monitored. Men with negative mpMRI and a higher risk of PCa (familial history, suspicious DRE, PSAD>0.20 ng/mL/cc or PSA>20 ng/mL) should be considered for systematic prostate biopsy. While PI-RADS 4-5 lesions represent a strong indication for prostate biopsy, PI-RADS 3 lesions should be further stratified according to PSAD values and prostate biopsy performed when PSAD is higher than 0.20. Accreditation, certification, and quality audits of radiologists and centers performing prostatic mpMRI should be strongly considered. The accessibility and/or the waiting list for MRI examinations should be also evaluated in the diagnostic pathway. The panel suggests performing transperineal or transrectal targeted plus systematic biopsies as standard of care.

Conclusions: Scientific societies must support the use of shared diagnostic pathway with the aim to increase the early detection of significant PCa reducing a delayed diagnosis of advanced PCa. Moreover, a shared diagnostic pathway can reduce the incorrect use of antibiotic, the number of unnecessary laboratory and radiologic examinations as well as of prostate biopsies.

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来源期刊
Minerva Urology and Nephrology
Minerva Urology and Nephrology UROLOGY & NEPHROLOGY-
CiteScore
8.50
自引率
32.70%
发文量
237
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