Target trial on the outcomes of laparoscopic compared to robotic-assisted proctectomy in stage II-III rectal cancer

针对II-III期直肠癌患者,比较腹腔镜直肠切除术与机器人辅助直肠切除术疗效的靶向试验

阅读:1

Abstract

Although outcomes of laparoscopic and robotic-assisted proctectomy have been compared, the superiority of one approach over another was not proven. We used the target trial methodology to emulate a randomized clinical trial comparing laparoscopic and robotic-assisted proctectomy for rectal cancer. Data from the NCDB (2015-2021) on patients with stage II-III rectal adenocarcinoma were collected. Patients were divided into two groups: laparoscopic proctectomy (LP) and robotic-assisted proctectomy (RP). The groups were matched for baseline patient and treatment confounders to obtain balanced groups, emulating the design of a randomized trial. The primary outcome was the pathologic outcomes of each surgical approach, including the status of circumferential resection margins (CRM), surgical margins, and number of examined lymph nodes. Secondary outcomes included conversion to open surgery, hospital stay, and 30- and 90-day mortality. After matching, 5631 patients were included in each group. The RP and LP groups had similar rates of positive CRM (10.5% vs. 9.4%, p = 0.072), positive surgical margins (6% vs. 6.3%, p = 0.528), examined lymph nodes number (median: 15 vs. 15, p = 0.105), 30-day mortality (0.7% vs. 0.9%, p = 0.405), 90-day mortality (1.5% vs. 1.8%, p = 0.333), and unplanned 30-day readmission (6.6% vs. 6.2%, p = 0.477). RP was associated with shorter hospital stay (median: 4 vs. 5 days, p < 0.001) and lower rate of conversion to open surgery (5.8% vs. 13.6%, OR: 0.39, 95%CI 0.34-0.45, p < 0.001). This target trial found RP and LP for rectal cancer associated with similar clinical and pathologic outcomes. RP was associated with fewer conversions and shorter hospital stays than LP.

特别声明

1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。

2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。

3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。

4、投稿及合作请联系:info@biocloudy.com。