Randomized Controlled Trial

Comparison of Laparoscopic Versus Robot-Assisted Surgery for Rectal Cancers

The COLRAR Randomized Controlled Trial

Park, Jun Seok MD, PhD*; Lee, Sung Min MD*; Choi, Gyu-Seog MD, PhD*; Park, Soo Yeun MD*; Kim, Hye Jin MD*; Song, Seung Ho MD*; Min, Byung Soh MD, PhD; Kim, Nam Kyu MD, PhD; Kim, Seon Hahn MD, PhD; Lee, Kang Young MD, PhD

Author Information
Annals of Surgery 278(1):p 31-38, July 2023. | DOI: 10.1097/SLA.0000000000005788

Abstract

Objective: 

To evaluate whether robotic for middle or low rectal cancer produces an improvement in surgical outcomes compared with laparoscopic surgery in a randomized controlled trial (RCT).

Background: 

There is a lack of proven clinical benefit of robotic total mesorectal excision (TME) compared with a laparoscopic approach in the setting of multicenter RCTs.

Methods: 

Between July 2011 and February 2016, patients diagnosed with an adenocarcinoma located <10 cm from the anal verge and clinically rated T1-4aNxM0 were enrolled. The primary outcome was the completeness of TME assessed by a surgeon and a pathologist.

Results: 

The RCT was terminated prematurely because of poor accrual of data. In all, 295 patients were assigned randomly to a robot-assisted TME group (151 in R-TME) or a laparoscopy-assisted TME group (144 in L-TME). The rates of complete TME were not different between groups (80.7% in R-TME, 77.1% in L-TME). Pathologic outcomes including the circumferential resection margin and the numbers of retrieved lymph nodes were not different between groups. In a subanalysis, the positive circumferential resection margin rate was lower in the R-TME group (0% vs 6.1% for L-TME; P=0.031). Among the recovery parameters, the length of opioid use was shorter in the R-TME group (P=0.028). There was no difference in the postoperative complication rate between the groups (12.0% for R-TME vs 8.3% for L-TME).

Conclusions: 

In patients with middle or low rectal cancer, robotic-assisted surgery did not significantly improve the TME quality compared with conventional laparoscopic surgery (ClinicalTrial.gov ID: NCT01042743).

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