A Randomized Open-Label, Noninferiority, Phase 3, Multicenter, Controlled Trial to Compare Laparoscopic Surgery With Open Surgery for Symptomatic, Noncurable Stage IV Colorectal Cancer (JCOG1107).

Tomonori Akagi, Masafumi Inomata, Ryo Kanzaka, Hiroshi Katayama, Haruhiko Fukuda, Akio Shiomi, Masaaki Ito, Jun Watanabe, Kohei Murata, Yasumitsu Hirano, Manabu Shimomura, Shunsuke Tsukamoto, Tetsuya Hamaguchi, Seigo Kitano, Yukihide Kanemitsu
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引用次数: 0

Abstract

Objective: To confirm noninferiority of laparoscopic (LAP) to open surgery (OP) for progression-free survival (PFS) of patients with non-curable stage IV colorectal cancer (CRC).

Background: Benefits of LAP versus OP are suggested, but long-term survival following LAP for symptomatic, noncurable CRC remains unclear.

Methods: In this open-label, multicenter, randomized controlled trial, only accredited surgeons from 42 Japanese institutions participated. Eligibility criteria included pathologically proven adenocarcinoma or adenosquamous carcinoma; primary tumor anywhere in the colon causing bowel stenosis and/or bleeding; and at least 1 to 3 noncurable factors. Patients received mFOLFOX6+bevacizumab or CapeOX+bevacizumab postoperatively and were randomly assigned 1:1 to the OP or LAP group. The primary endpoint was PFS, with noninferiority margin for the hazard ratio (HR) set at 1.38.

Results: Between January 2013 and January 2021, 195 patients were randomized (OP, n = 95, LAP, n = 100). Ninety-two patients received OP and 98 LAP, with 82 OP and 86 LAP patients receiving postoperative chemotherapy. Median PFS was 9.7 months (95% CI = 8.7-11.3) for OP and 10.4 months (9.1-12.4) for LAP. Noninferiority of LAP was confirmed [HR = 1.02; 91.4% CI = 0.79-1.32 (<1.38), P for noninferiority = 0.021]. Median overall survival was 23.9 months (95% CI = 18.6-29.4) for OP and 25.4 months (19.4-29.0) for LAP (HR = 0.99; 95% CI, 0.72-1.36). In-hospital mortality was 1.1% (OP) and 0% (LAP). Postoperative complications (Grade 2-4) included ileus (OP = 12.0%; LAP = 5.1%), wound infection (OP = 2.2%; LAP = 2.0%), and anastomotic leakage (OP = 0%; LAP = 2.0%).

Conclusions: LAP appears to be an acceptable standard treatment for symptomatic, noncurable stage IV CRC.

Trial registration: UMIN-CTR, number UMIN000009715.

Abstract Image

Abstract Image

一项随机、开放标签、非劣效性、3期、多中心、对照试验,比较腹腔镜手术与开放手术治疗有症状的、无法治愈的IV期结直肠癌(JCOG1107)。
目的:探讨腹腔镜手术(LAP)对IV期结直肠癌(CRC)患者无进展生存(PFS)的非低效性。背景:LAP相对于OP的益处已被提出,但对于有症状的、无法治愈的结直肠癌,LAP后的长期生存仍不清楚。方法:在这项开放标签、多中心、随机对照试验中,只有来自42家日本机构的经认证的外科医生参与。入选标准包括病理证实的腺癌或腺鳞癌;结肠任何部位的原发肿瘤,引起肠狭窄和/或出血;至少有1到3个不可治愈的因素。患者术后接受mFOLFOX6+贝伐单抗或CapeOX+贝伐单抗治疗,按1:1随机分为OP组或LAP组。主要终点为PFS,风险比(HR)的非劣效性边际为1.38。结果:2013年1月至2021年1月,195例患者随机入选(OP, n = 95, LAP, n = 100)。OP 92例,LAP 98例,OP 82例,LAP 86例,术后化疗。OP的中位PFS为9.7个月(95% CI = 8.7-11.3), LAP为10.4个月(9.1-12.4)。证实LAP的非劣效性[HR = 1.02;91.4% CI = 0.79-1.32(非劣效性P = 0.021)。OP的中位总生存期为23.9个月(95% CI = 18.6-29.4), LAP的中位总生存期为25.4个月(19.4-29.0)(HR = 0.99;95% ci, 0.72-1.36)。住院死亡率分别为1.1% (OP)和0% (LAP)。术后并发症(2-4级)包括肠梗阻(OP = 12.0%;LAP = 5.1%),伤口感染(OP = 2.2%;LAP = 2.0%),吻合口漏(OP = 0%;圈= 2.0%)。结论:LAP似乎是一种可接受的标准治疗有症状的,无法治愈的IV期结直肠癌。试验注册号:UMIN-CTR,编号:UMIN000009715。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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