Department of Colorectal Surgery, Tokyo Medical University Hospital, Tokyo, Japan.
Department of Surgery, Tochigi Cancer Centre, Tochigi, Japan.
Br J Surg. 2020 Apr;107(5):586-594. doi: 10.1002/bjs.11513. Epub 2020 Mar 12.
Japan Clinical Oncology Group (JCOG) 0212 (ClinicalTrials.gov NCT00190541) was a non-inferiority phase III trial of patients with clinical stage II-III rectal cancer without lateral pelvic lymph node enlargement. The trial compared mesorectal excision (ME) with ME and lateral lymph node dissection (LLND), with a primary endpoint of recurrence-free survival (RFS). The planned primary analysis at 5 years failed to confirm the non-inferiority of ME alone compared with ME and LLND. The present study aimed to compare ME alone and ME with LLND using long-term follow-up data from JCOG0212.
Patients with clinical stage II-III rectal cancer below the peritoneal reflection and no lateral pelvic lymph node enlargement were included in this study. After surgeons confirmed R0 resection by ME, patients were randomized to receive ME alone or ME with LLND. The primary endpoint was RFS.
A total of 701 patients from 33 institutions were assigned to ME with LLND (351) or ME alone (350) between June 2003 and August 2010. The 7-year RFS rate was 71.1 per cent for ME with LLND and 70·7 per cent for ME alone (hazard ratio (HR) 1·09, 95 per cent c.i. 0·84 to 1·42; non-inferiority P = 0·064). Subgroup analysis showed improved RFS among patients with clinical stage III disease who underwent ME with LLND compared with ME alone (HR 1·49, 1·02 to 2·17).
Long-term follow-up data did not support the non-inferiority of ME alone compared with ME and LLND. ME with LLND is recommended for patients with clinical stage III disease, whereas LLND could be omitted in those with clinical stage II tumours.
日本临床肿瘤学组(JCOG)0212 (ClinicalTrials.gov NCT00190541)是一项针对无侧盆淋巴结肿大的临床 II-III 期直肠癌患者的非劣效性 III 期临床试验。该试验比较了直肠系膜切除术(ME)与 ME 加侧方淋巴结清扫术(LLND),主要终点为无复发生存率(RFS)。计划在 5 年内进行的主要分析未能证实 ME 单独与 ME 和 LLND 相比无劣效性。本研究旨在使用 JCOG0212 的长期随访数据比较 ME 单独与 ME 和 LLND。
本研究纳入了腹膜反射以下临床 II-III 期直肠癌且无侧盆淋巴结肿大的患者。在外科医生确认 ME 达到 R0 切除后,患者被随机分配接受 ME 单独或 ME 加 LLND。主要终点为 RFS。
共有来自 33 家机构的 701 例患者被分配至 ME 加 LLND(351 例)或 ME 单独(350 例)组,分配时间为 2003 年 6 月至 2010 年 8 月。ME 加 LLND 和 ME 单独的 7 年 RFS 率分别为 71.1%和 70.7%(危险比(HR)1.09,95%置信区间(CI)0.84 至 1.42;非劣效性 P=0.064)。亚组分析显示,在接受 ME 加 LLND 的 III 期疾病患者中,RFS 得到改善,与 ME 单独组相比(HR 1.49,1.02 至 2.17)。
长期随访数据不支持 ME 单独与 ME 和 LLND 相比无劣效性。对于 III 期疾病患者,建议行 ME 加 LLND;而对于 II 期肿瘤患者,可省略 LLND。