Department of Urology, Institut Mutualiste Montsouris and Université Paris Descartes, Paris, France; Department of Surgical Sciences, University of Turin and Città della Salute e della Scienza, Turin Italy; Department of Urology and Clinical Research Group on predictive onco-urology, APHP. Sorbonne University, Paris, France.
Department of Urology, St. Antonius Hospital, Nieuwegein and Utrecht, The Netherlands.
Clin Genitourin Cancer. 2022 Dec;20(6):592-604. doi: 10.1016/j.clgc.2022.06.009. Epub 2022 Jun 30.
INTRODUCTION/BACKGROUND: Only 1 randomized controlled trial has compared focal therapy and active surveillance (AS) for the low-risk prostate cancer (PCa). We investigated whether focal HIFU (fHIFU) yields oncologic advantages over AS for low-risk PCa.
We included 2 non-randomized prospective series of 132 (fHIFU) and 421 (AS) consecutive patients diagnosed with ISUP 1 PCa between 2008 and 2018. A matched pair analysis was performed to decrease potential bias. Study main outcomes were freedom from radical treatment (RT) or androgen-deprivation therapy (ADT), treatment-free survival (TFS), time to metastasis, and overall survival (OS).
Median fHIFU follow-up was 50 months (interquartile range, 29-84 months). Among matched variables, no major differences were recorded except for AS having more suspicious digital rectal examination findings (P = .0074) and recent enrollment year (P = .0005). Five-year intervention-free survival from RT or ADT was higher for the fHIFU cohort (67.4% vs. 53.8%; P = .0158). Time to treatment was approximately 10 months shorter for AS than for fHIFU (time to RT, P = .0363; time to RT or ADT, P = .0156; time to any treatment, P = .0319). No differences were found in any-TFS (fHIFU, 61.4% vs. AS, 53.8%; P = .2635), OS (fHIFU, 97% vs. AS, 97%; P = .9237), or metastasis (n = 0 in fHIFU and n = 2 in AS; P = .4981). Major complications (≥ Clavien 3) were rare (n = 4), although 36.4% of men experienced complications. No relevant changes were noted in continence (P = .3949).
At a 4-year median follow-up, fHIFU for mainly low-risk PCa (ISUP grade 1) is safe, may decrease the need for radical treatment or ADT and may allow longer time to treatment compared to AS. Nonetheless, no advantages are seen in PCa progression and/or death (OS).
简介/背景:仅有 1 项随机对照试验比较了低危前列腺癌(PCa)的局部治疗和主动监测(AS)。我们研究了低危 PCa 中,局灶高强度聚焦超声(fHIFU)治疗是否优于 AS。
我们纳入了 2008 年至 2018 年间连续诊断为 ISUP 1 级 PCa 的 132 例(fHIFU)和 421 例(AS)非随机前瞻性系列患者。为了降低潜在的偏倚,我们进行了配对分析。研究的主要结局是免于根治性治疗(RT)或雄激素剥夺治疗(ADT)、无治疗生存(TFS)、转移时间和总生存(OS)。
中位 fHIFU 随访时间为 50 个月(四分位距,29-84 个月)。在配对变量中,除了 AS 有更多可疑的直肠指检发现(P = .0074)和最近的入组年份(P = .0005)外,没有记录到其他主要差异。fHIFU 组的 5 年无 RT 或 ADT 干预生存率更高(67.4% vs. 53.8%;P = .0158)。AS 组的治疗时间比 fHIFU 组约早 10 个月(RT 时间,P = .0363;RT 或 ADT 时间,P = .0156;任何治疗时间,P = .0319)。无 TFS(fHIFU,61.4% vs. AS,53.8%;P = .2635)、OS(fHIFU,97% vs. AS,97%;P = .9237)或转移(fHIFU 无转移,n=0;AS 有 2 例转移,n=2;P = .4981)方面无差异。(≥Clavien 3 级)主要并发症罕见(n = 4),但 36.4%的患者出现并发症。尿控无明显变化(P = .3949)。
在中位随访 4 年时,主要为低危 PCa(ISUP 1 级)的 fHIFU 治疗安全,与 AS 相比,可能减少根治性治疗或 ADT 的需要,并可能延长治疗时间。然而,在 PCa 进展和/或死亡(OS)方面没有优势。