The role of androgen deprivation therapy prior to radical prostatectomy in high-risk prostate cancer: a systematic review

前列腺癌 雄激素剥夺疗法 前列腺切除术 医学 激素疗法 系统回顾 随机对照试验 科克伦图书馆 观察研究 病态的 肿瘤科 抗雄激素 梅德林 临床试验 内科学 癌症 政治学 法学
作者
Yenny ARROYO-ROJAS,Lara Rodríguez‐Sánchez,Gianmarco Colandrea,Hugo Otaola-Arca,Camille Lanz,Éric Barret,Rafael Sánchez-Salas,Petr Macek,Xavier Cathelineau
出处
期刊:Minerva urology and nephrology [Edizioni Minerva Medica]
卷期号:76 (2)
标识
DOI:10.23736/s2724-6051.24.05630-1
摘要

INTRODUCTION: Patients with high-risk prostate cancer (HRPCa) are prone to have worse pathological features, resulting in early biochemical recurrence after radical prostatectomy (RP). There is an urgent need to develop novel treatment strategies for this group of patients to optimize their outcomes. The purpose of this study is to perform a systematic review of the role of neoadjuvant hormonal therapy (NHT) followed by RP in HRPCa patients.EVIDENCE ACQUISITION: We performed a systematic review of the following databases, MEDLINE (PubMed), EMBASE, Cochrane Library, and clinical Trial.gov; between January 2007 and August 2023, following the PRISMA guidelines.EVIDENCE SYNTHESIS: After screening and deduplication, we included ten studies from an initial pool of 1275. The risk of bias was low in observational studies but ranged from moderate to low in controlled trials. Five studies utilized traditional androgen deprivation treatments (ADT), revealing favorable pathological outcomes but inconsistency in evaluating oncological results. Additionally, four studies focused on RP combined with androgen receptor pathway inhibitors (ARPIs) in the NHT setting, all showing primarily positive pathological outcome, with no clear evidence of an oncological benefit. Limited long-term follow-up data and a shortage of randomized controlled trials were evident among all the studies included in this review, regardless of the type of hormonal treatment used.CONCLUSIONS: Different hormonal treatments, including traditional ADT and ARPIs, yield positive pathology outcomes. Oncological evidence remains limited, echoing older findings predating ARPIs. Definitive conclusions require longer follow-ups and precise patient selection. Currently, insufficient evidence support ARPIs' superiority over conventional therapy before RP.
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