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四项疗程与八项疗程辅助 S-1 治疗 II 期胃癌患者(JCOG1104 [OPAS-1]):一项开放标签、III 期、非劣效性、随机试验。

Four courses versus eight courses of adjuvant S-1 for patients with stage II gastric cancer (JCOG1104 [OPAS-1]): an open-label, phase 3, non-inferiority, randomised trial.

机构信息

Department of Gastric Surgery, National Cancer Center Hospital, Chuo-Ku, Tokyo, Japan.

Division of Gastric Surgery, Shizuoka Cancer Center, Nagaizumi-cho, Sunto-gun, Shizuoka Prefecture, Japan.

出版信息

Lancet Gastroenterol Hepatol. 2019 Mar;4(3):208-216. doi: 10.1016/S2468-1253(18)30383-2. Epub 2019 Jan 22.

Abstract

BACKGROUND

Postoperative adjuvant chemotherapy with S-1 for 1 year (corresponding to eight courses) is standard care for stage II gastric cancer. Whether the duration of S-1 could be shortened to 6 months (corresponding to four courses) without worsening survival is unclear. The aim of this study was to investigate the non-inferiority of four courses of S-1 compared with eight courses of S-1 for patients with stage II gastric cancer.

METHODS

We did a phase 3, open-label, randomised controlled, non-inferiority trial at 59 hospitals in Japan. Patients aged 20-80 years with stage II adenocarcinoma of the stomach were randomly assigned (1:1) to eight courses or four courses of S-1. Randomisation was done by the Japan Clinical Oncology Group Data Center website, using a minimisation method with a random component using institution, stage (IIA vs IIB), age (<70 years vs ≥70 years), and mode of operation (open gastrectomy with bursectomy vs open gastrectomy without bursectomy vs laparoscopic gastrectomy) as adjustment factors. One course was 80 mg/day per m of S-1 administered for 4 weeks followed by a rest for 2 weeks. The primary endpoint was relapse-free survival, analysed by intention to treat, with a non-inferiority margin for the hazard ratio (HR) set at 1·37. This study is registered at UMIN-Clinical Trial Registry, number UMIN000007306.

FINDINGS

Between Feb 16, 2012, and March 19, 2017, 590 patients were enrolled (295 per group). 528 (89%) patients were analysed at the first planned interim analysis in March, 2017, at which time the point estimate of HR for the four-course group compared with the eight-course group was 2·52 (95% CI 1·11-5·77), which exceeded 1·37 and met the prespecified criteria for early termination. Predictive probability for showing non-inferiority at the final analysis was calculated to be 2·9%. The study was stopped for futility. Updated 3-year relapse-free survival analysed in May, 2017, was 93·1% (95% CI 87·8-96·1) for the eight-course group and 89·8% (84·2-93·5) for the four-course group (HR 1·84, 95% CI 0·93-3·63). The most common grade 3-4 adverse event was neutropenia, observed in 46 (16%) patients in the eight-course group and 51 (17%) patients in the four-course group.

INTERPRETATION

S-1 for 1 year should remain as standard adjuvant chemotherapy for stage II gastric cancer.

FUNDING

Japan Agency for Medical Research and Development; the Ministry of Health, Labour and Welfare of Japan; the National Cancer Center Research and Development Fund, Japan.

摘要

背景

对于 II 期胃癌患者,术后辅助化疗 1 年(对应 8 个疗程)是标准治疗方案。S-1 的疗程能否缩短至 6 个月(对应 4 个疗程)而不影响生存尚未明确。本研究旨在探讨 S-1 4 个疗程对比 8 个疗程对 II 期胃癌患者的非劣效性。

方法

我们在日本 59 家医院进行了一项 3 期、开放标签、随机对照、非劣效性试验。年龄在 20-80 岁之间、患有 II 期腺癌的胃癌患者被随机分配(1:1)接受 S-1 8 个疗程或 4 个疗程治疗。通过日本临床肿瘤学组数据中心网站,采用最小化方法,以机构、分期(IIA 与 IIB)、年龄(<70 岁与≥70 岁)和手术方式(开腹胃切除术+胆囊切除术与开腹胃切除术-胆囊切除术与腹腔镜胃切除术)作为调整因素进行随机分组。一个疗程为 80mg/m2 S-1 每天,持续 4 周,然后休息 2 周。主要终点为无复发生存期,通过意向治疗进行分析,设定 HR 的非劣效性边界为 1.37。该研究在 UMIN-临床试验注册中心注册,编号为 UMIN000007306。

结果

2012 年 2 月 16 日至 2017 年 3 月 19 日期间,共纳入 590 例患者(每组 295 例)。2017 年 3 月,进行了第一次计划的中期分析,共有 528 例(89%)患者入组。此时,4 个疗程组与 8 个疗程组的 HR 点估计值为 2.52(95%CI 1.11-5.77),超过了 1.37,符合提前终止的预设标准。最终分析时显示非劣效性的预测概率计算为 2.9%。由于无效,该研究停止。2017 年 5 月更新的 3 年无复发生存率分析显示,8 个疗程组为 93.1%(95%CI 87.8-96.1),4 个疗程组为 89.8%(84.2-93.5)(HR 1.84,95%CI 0.93-3.63)。最常见的 3-4 级不良事件为中性粒细胞减少症,8 个疗程组中有 46 例(16%)患者发生,4 个疗程组中有 51 例(17%)患者发生。

解释

S-1 1 年的治疗方案应继续作为 II 期胃癌的标准辅助化疗方案。

资金来源

日本医疗研究与开发机构;日本厚生劳动省;日本国家癌症中心研发基金。

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