Operative Details and Oncological and Functional Outcome of Robotic-Assisted Laparoscopic Radical Prostatectomy: 400 Cases with a Minimum of 12 Months Follow-up

被引:141
作者
Murphy, Declan G. [1 ]
Kerger, Michael [1 ]
Crowe, Helen [1 ]
Peters, Justin S. [1 ]
Costello, Anthony J. [1 ]
机构
[1] Royal Melbourne Hosp, Dept Urol, Parkville, Vic 3052, Australia
关键词
da Vinci; Laparoscopic; Prostate cancer; Radical prostatectomy; Robotic; Technique;
D O I
10.1016/j.eururo.2008.12.035
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
Background: Robotic-assisted laparoscopic radical prostatectomy (RALP) using the da Vinci (R) surgical system (Intuitive Surgical, Sunnyvale, CA) is increasingly used for the management of localised prostate cancer. Objective: We report the operative details and short-term oncological and functional outcome of the first 400 RALPs; performed at our unit. Design, setting and participants: From December 2003 to August 2006, 400 consecutive patients underwent RALP at our institution. A prospective database was established to record the relevant details of all RALP cases. Surgical procedure: A six port transperitoneal approach using a 4-arm da Vinci (R) system was used to perform RALP. This database was reviewed to establish the operative details and oncological and functional outcome of all patients with a minimum of 12 months follow-up. Measurements: Perioperative characteristics and outcomes are reported. Functional outcome was assessed using continence and erectile function questionnaires. Biochemical recurrence (prostate-specific antigen (PSA) >= 0.2 ng/mL) is used as a surrogate for cancer control. Results and limitations: The mean age standard deviation (SD) was 60.2 +/- 6 years. Median PSA level was 7.0 (interquartile range (IQR) 5.3-9.6) ng/mL. The mean operating time +/-SD was 186 +/- 49 mins. The complication rate was 15.75% comprising Clavien grade I-II and Clavien grade III complications in 10.5% and 5.25% of patients respectively. The overall positive surgical margin rate was 19.2% with T2 and T3 positive margin rates of 9.6% and 42.3% respectively. The biochemical recurrence-free survival was 86.6% at a median follow-up of 22 (IQR = 15-30) months. At 12 months follow-up, 91.4% of patients were pad-free or used a security liner. of those men previously potent (defined as Sexual Health Inventory for Men [SHIM] score >= 21) who underwent nerve-sparing RALP, 62% were potent at 12 months. Conclusions: The safety and feasibility of RALP has already been established. Our initial experience with this procedure shows promising short-term outcomes. (C) 2008 European Association of Urology. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:1358 / 1367
页数:10
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