Department of Abdominal Surgery, Zhejiang Cancer Hospital (University of Chinese Academy of Sciences Cancer Hospital), Zhejiang, China.
Department of General Surgery, Second Affiliated Hospital of Medical College of Zhejiang University, Zhejiang, China.
BMC Cancer. 2021 Jan 12;21(1):56. doi: 10.1186/s12885-020-07772-7.
Surgery is the only treatment option for operable gastric cancer. The CLASSIC and ACTS-GC studies showed that the 5-year overall survival (OS) of patients with stage III gastric cancer undergoing D2 gastrectomy is still very low. Whether adjuvant nanoparticle albumin-bound paclitaxel (nab-paclitaxel) combined chemotherapy is more effective than the XELOX standard adjuvant chemotherapy in patients with stage III gastric cancer has not been confirmed.
This is a multicenter, open-label, phase III clinical study. In this trial, 616 patients with locally advanced stage III gastric cancer that underwent curative D2 radical surgery and achieved R0 are planned to be included. Patients will be randomized 1:1 to nab-paclitaxel combined with S-1 (AS) vs. oxaliplatin combined with capecitabine (XELOX). XELOX group: Patients assigned to the XELOX group received eight 3-week cycles of oral capecitabine (1000 mg/m) twice daily on days 1-14 of each cycle plus intravenous oxaliplatin 130 mg/m on day 1 of each cycle. AS group: AS group received eight 3-week cycles of oral S-1 (80-120 mg) (< 1.25 m, 40 mg; 1.25 to < 1.5 m, 50 mg; and > 1.5 m, 60 mg) twice daily on days 1-14 plus intravenous nab-paclitaxel 120 mg/m on days 1 and 8 of each cycle. The primary endpoint was the 3-year disease-free survival (3-year-DFS) defined as the time from randomisation to the time of recurrence of the original gastric cancer, development of a new gastric cancer, or death from any cause. The secondary endpoints were the overall survival, (defined as the time from the date of randomisation to date of death from any cause) and safety (any adverse event).
Compared with previous studies, this study includes nab-paclitaxel based on S-1 adjuvant chemotherapy, which is expected to achieve better efficacy and lower toxicity than the standard treatment. This study is the first clinical study to evaluate the safety and efficacy of nab-paclitaxel combined with S-1 in patients with stage III gastric cancer after D2 radical resection.
This clinical trial has been registered with ClinicalTrials.gov, registration number: NCT04135781 , on October 20th, 2019.
手术是可切除胃癌的唯一治疗选择。CLASSIC 和 ACTS-GC 研究表明,接受 D2 胃切除术的 III 期胃癌患者的 5 年总生存率(OS)仍然很低。对于 III 期胃癌患者,纳米白蛋白结合紫杉醇(nab-紫杉醇)联合辅助化疗是否比 XELOX 标准辅助化疗更有效尚未得到证实。
这是一项多中心、开放标签、III 期临床研究。在这项试验中,计划纳入 616 例局部晚期 III 期胃癌患者,这些患者接受了根治性 D2 根治性手术,达到了 R0。患者将以 1:1 的比例随机分为 nab-紫杉醇联合 S-1(AS)组与奥沙利铂联合卡培他滨(XELOX)组。XELOX 组:分配至 XELOX 组的患者接受 8 个 3 周周期的口服卡培他滨(1000mg/m),每日 2 次,于每个周期的第 1-14 天给药,以及每个周期第 1 天静脉注射奥沙利铂 130mg/m。AS 组:AS 组接受 8 个 3 周周期的口服 S-1(80-120mg)(<1.25m,40mg;1.25 至<1.5m,50mg;>1.5m,60mg),每日 2 次,于每个周期的第 1-14 天给药,以及每个周期第 1 和第 8 天静脉注射 nab-紫杉醇 120mg/m。主要终点是无病生存期(3 年-DFS),定义为随机分组至原胃癌复发、新发胃癌或任何原因死亡的时间。次要终点是总生存期(定义为随机分组至任何原因死亡的时间)和安全性(任何不良事件)。
与既往研究相比,本研究包含基于 S-1 的 nab-紫杉醇辅助化疗,预计比标准治疗具有更好的疗效和更低的毒性。本研究是第一项评估 D2 根治性切除术后 III 期胃癌患者接受 nab-紫杉醇联合 S-1 治疗的安全性和疗效的临床研究。
本临床试验于 2019 年 10 月 20 日在 ClinicalTrials.gov 上注册,注册号:NCT04135781。