Division of Surgery and Interventional Science, University College London, London, United Kingdom.
Cancer. 2012 Sep 1;118(17):4148-55. doi: 10.1002/cncr.27394. Epub 2012 Jan 3.
The objective of this study was to evaluate the safety, feasibility, side-effect profile, and proof of concept for focal salvage therapy using high-intensity focused ultrasound (HIFU).
A registry-based analysis was conducted between 2004 and 2009 of 430 patients who underwent HIFU. Thirty-nine patients received focal salvage therapy for localized recurrence after external beam radiotherapy. Multiparametric magnetic resonance imaging studies combined with transperineal template prostate mapping biopsies or transrectal biopsies were used to localize disease. Validated questionnaires were used to assess functional outcomes. Biochemical failure was defined by using both Phoenix criteria (prostate-specific antigen [PSA] nadir plus 2 ng/mL) and Stuttgart criteria (PSA nadir plus 1.2 ng/mL).
The mean pre-HIFU PSA level was 4.6 ng/mL. The median follow-up was 17 months (interquartile range, 10-29 months). International Index of Erectile Function-5 scores decreased from a median ± standard deviation (SD) of 18 ± 16 to 13 ± 21 at 6 months, demonstrating worsening function. Scores on the University of California Los Angeles-Expanded Prostate Cancer Index Composite Urinary domain indicate that pad-free, leak-free continence status was 64%, and the pad-free rate was 87.2% at last follow-up. One rectourethral fistula occurred and spontaneously resolved with urinary and bowel diversion. The actuarial progression-free survival rate (including PSA nonresponders) was 69% at 1 year and 49% at 2 years according to Phoenix criteria. Excluding PSA nonresponders, these rates were 74% and 58%, respectively (Phoenix criteria).
The results from this study indicated that focal salvage therapy is a potential strategy for localized recurrence after radiotherapy that may reduce the harms resulting from whole-gland salvage therapies.
本研究旨在评估高强度聚焦超声(HIFU)局部挽救治疗的安全性、可行性、副作用谱和概念验证。
对 2004 年至 2009 年间接受 HIFU 治疗的 430 例患者进行了基于登记的分析。39 例患者在接受外照射放疗后出现局限性复发,接受了局部挽救治疗。多参数磁共振成像研究结合经会阴模板前列腺图谱活检或经直肠活检用于定位疾病。使用验证后的问卷评估功能结果。生化失败定义为同时采用凤凰标准(PSA 最低值加 2ng/ml)和斯图加特标准(PSA 最低值加 1.2ng/ml)。
HIFU 前 PSA 平均水平为 4.6ng/ml。中位随访时间为 17 个月(四分位距 10-29 个月)。国际勃起功能指数-5 评分从治疗前中位数±标准差(SD)的 18±16 降至 6 个月时的 13±21,表明功能恶化。加利福尼亚大学洛杉矶分校前列腺癌指数综合尿域扩展量表的评分表明,无垫尿失禁状态为 64%,最后一次随访时无垫尿失禁率为 87.2%。1 例直肠尿道瘘发生,经尿便转流后自发愈合。根据凤凰标准,1 年时无进展生存率(包括 PSA 无应答者)为 69%,2 年时为 49%。排除 PSA 无应答者后,这些比率分别为 74%和 58%(凤凰标准)。
本研究结果表明,对于放疗后局部复发,局部挽救治疗可能是一种潜在策略,可以减少全腺体挽救治疗带来的危害。