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Active surveillance for intermediate‐risk prostate cancer: a systematic review and pooled analysis

医学 荟萃分析 合并分析 前列腺癌 置信区间 内科学 中止 前列腺 肿瘤科 系统回顾 妇科 梅德林 前列腺活检 危险系数 生存分析 科学网 总体生存率 队列 小心等待 合并方差 队列研究 缺少数据 疾病 活检 子群分析 癌症 过度诊断 一致性 出版偏见
作者
Alessandro Uleri,Ludovica Cella,Thibaut Long Depaquit,Federica Sordelli,Alba Farré,Víctor Caballero,Josep Comet,Pawel Rajwa,Romain Diamand,Bertrand Tombal,Morgan Roupret,V Kasivisvanathan,Michael S. Leapman,Guillaume Ploussard,Michael Baboudjian
出处
期刊:BJUI [Wiley]
标识
DOI:10.1111/bju.70388
摘要

OBJECTIVE: Active surveillance (AS) is the preferred management for individuals with low-risk prostate cancer (PCa), but its role in intermediate-risk (IR) disease remains underreported. Given growing interest and published data, we performed an updated systematic review and meta-analysis to evaluate AS outcomes in selected patients with Gleason Grade Group (GG) 1-2 IR PCa. METHODS: A systematic review was conducted according to Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines (PROSPERO CRD420251138532). PubMed/MEDLINE, Embase, and Web of Science databases were searched for studies published up to September 2025 reporting outcomes of AS in IR PCa. Primary outcomes were AS discontinuation-free survival and GG ≥3 upgrade-free survival. RESULTS: In total, 18 studies, including 3783 selected patients with IR PCa, were analyzed. Pooled AS discontinuation-free survival rates were 70% (95% confidence interval [CI] 62-78) at 3 years, 63% (95% CI 58-68) at 5 years, and 53% (95% CI 38-67) at 10 years. In analyses restricted to GG 2 cohorts, corresponding pooled estimates were 72% at 3 years, 56% at 5 years, and 40% at 10 years. GG ≥3 upgrade-free survival was 84% (95% CI 76-92) at 3 years and 78% (95% CI 65-91) at 5 years in all cohorts and 92% (95% CI 86-98) and 87% (95% CI 78-95) at 3 and 5 years in cohorts screened using multiparametric magnetic resonance imaging. No significant difference in AS discontinuation was observed between biopsy GG 1 and 2 (hazard ratio 1.08; 95% CI 0.86-1.35). Limitations include moderate risk of bias and heterogeneity across AS protocols. CONCLUSIONS: Although long-term data are lacking, particularly regarding robust oncological outcomes, growing evidence suggests that AS appears oncologically safe in well-selected patients. Magnetic resonance imaging will play a key role in the appropriate selection and follow-up of patients.
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