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RAFT 试验结果:局部治疗后的机器人手术。

Outcomes of the RAFT trial: robotic surgery after focal therapy.

机构信息

Department of Urology, Guys & St. Thomas' Hospital, London, UK.

Department of Urology, University College Hospital London, London, UK.

出版信息

BJU Int. 2021 Oct;128(4):504-510. doi: 10.1111/bju.15432. Epub 2021 May 13.

Abstract

OBJECTIVES

To report toxicity of treatment observed in men participating in the Robotic surgery After Focal Therapy (RAFT) clinical trial.

PATIENTS AND METHODS

Men were eligible for this prospective single group interventional study if they had histologically confirmed recurrent/residual prostate adenocarcinoma following primary FT. The short-form Expanded Prostate Cancer Index Composite (EPIC-26) measured prior to salvage robotic prostatectomy (S-RARP) and 3-monthly post-operatively together with Clavien-Dindo complications (I-IV). Secondary outcomes included biochemical recurrence-free survival (BCFS) following surgery and need for salvage treatment after surgery. This study is registered with ClinicalTrials.gov NCT03011606.

RESULTS

Twenty-four men were recruited between February 2016 and September 2018. 1 patient withdrew from the trial after consenting and before S-RARP. 23 men completed 12-month post S-RARP follow-up. Median EPIC-26 urinary continence scores initially deteriorated after 3 months (82.4 vs 100) but there was no statistically significant difference from baseline at 12 months (100 vs 100, P = 0.31). Median lower urinary tract symptom scores improved after 12 months compared to baseline (93.8 vs 87.5, P = 0.01). At 12 months, 19/23 (83%) were pad-free and 22/23 (96%) required 0/1 pads. Median sexual function subscale scores deteriorated and remained low at 12 months (22.2 vs 58.3, P < 0.001). Utilising a minimally important difference of nine points, at 12 months after surgery 17/23 (74%) reported urinary continence to be 'better' or 'not different' to pre-operative baseline. The corresponding figure for sexual function (utilising a minimally important difference of 12 points) was 7/23 (30%). There was no statistically significant difference on median bowel/hormonal subscale scores. Only a single patient had a post-operative complication (Clavien-Dindo Grade I). BCFS at 12 months after surgery was 82.6% (95% confidence interval [CI]: 60.1-93.1%) while 4/23 (17%) received salvage radiation.

CONCLUSIONS

The RAFT clinical trial suggests toxicity of surgery after FT is low, with good urinary function outcomes, albeit sexual function deteriorated overall. Oncological outcomes at 12 months appear acceptable.

摘要

目的

报告参与机器人手术后局部治疗(RAFT)临床试验的男性患者的治疗观察毒性。

患者和方法

如果男性在首次 FT 后经组织学证实有复发性/残留前列腺腺癌,则有资格参加这项前瞻性单组干预研究。在挽救性机器人前列腺切除术(S-RARP)前和术后 3 个月使用简化版扩展前列腺癌指数综合评分(EPIC-26)进行评估,并使用 Clavien-Dindo 并发症(I-IV 级)进行评估。次要结局包括术后生化无复发生存率(BCFS)和术后需要挽救性治疗。本研究在 ClinicalTrials.gov 注册,编号为 NCT03011606。

结果

2016 年 2 月至 2018 年 9 月期间共招募了 24 名男性。1 名患者在同意并接受 S-RARP 前退出了试验。23 名男性完成了 S-RARP 术后 12 个月的随访。术后 3 个月时,尿控的 EPIC-26 尿失禁评分最初恶化(82.4 分比 100 分),但与基线相比,12 个月时无统计学差异(100 分比 100 分,P = 0.31)。与基线相比,12 个月时下尿路症状评分有所改善(93.8 分比 87.5 分,P = 0.01)。12 个月时,23 名男性中有 19 名(83%)不再使用尿垫,22 名(96%)仅使用 0/1 片尿垫。术后 12 个月时,性健康功能子量表评分恶化且一直较低(22.2 分比 58.3 分,P < 0.001)。使用 9 分的最小临床重要差异,术后 12 个月时,23 名男性中有 17 名(74%)报告尿控“更好”或“与术前基线无差异”。性健康功能(使用 12 分的最小临床重要差异)的相应数字为 7/23(30%)。肠道/激素功能子量表评分无统计学差异。仅 1 名患者发生术后并发症(Clavien-Dindo 分级 I)。术后 12 个月的 BCFS 为 82.6%(95%置信区间[CI]:60.1%-93.1%),而 4/23 名(17%)接受了挽救性放疗。

结论

RAFT 临床试验表明,FT 后手术的毒性较低,尿功能结局良好,尽管总体上性功能恶化。12 个月时的肿瘤学结局似乎可以接受。

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