Outcomes of the RAFT trial: robotic surgery after focal therapy

被引:8
作者
Cathcart, Paul [1 ]
Ribeiro, Luis [1 ]
Moore, Caroline [2 ]
Ahmed, Hashim U. [3 ,4 ]
Leslie, Tom [5 ]
Arya, Manit [2 ,4 ]
Orczyk, Clement [2 ]
Hindley, Richard G. [6 ]
Cahill, Fidelma [1 ]
Prendergast, Aaron [7 ]
Coetzee, Carike [7 ]
Yogeswaran, Yathushan [7 ]
Tunna, Kirsty [7 ]
Sooriakumaran, Prasanna [2 ]
Emberton, Mark [2 ]
机构
[1] Guys & St Thomas Hosp, Dept Urol, London, England
[2] Univ Coll London Hosp, Dept Urol, London, England
[3] Imperial Coll London, Fac Med, Dept Surg & Canc, Imperial Prostate, London, England
[4] Imperial Coll Healthcare NHS Trust, Imperial Urol, London, England
[5] Oxford Univ Hosp, Dept Urol, Oxford, England
[6] Basingstoke & North Hampshire Hosp, Dept Urol, Basingstoke, Hants, England
[7] Queen Mary Univ London, Barts Canc Inst, Ctr Expt Canc Med, London, England
关键词
prostate cancer; focal therapy; salvage prostatectomy; robotic surgery; HIFU; #uroonc; #PCSM; #ProstateCancer; EXPANDED PROSTATE-CANCER; QUALITY-OF-LIFE; VALIDATION;
D O I
10.1111/bju.15432
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
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.
引用
收藏
页码:504 / 510
页数:7
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