Department of General Surgery & Institute of General Surgery, Chinese PLA General Hospital, No.28 Fuxing Road, Haidian District, Beijing, 100853, China.
Department of General Surgery, Zhongshan Hospital, Fudan University, No.180 Fenglin Road, Xuhui District, Shanghai, 200032, China.
BMC Cancer. 2021 Jan 5;21(1):20. doi: 10.1186/s12885-020-07764-7.
Curing locally advanced gastric cancer through surgery alone is difficult. Adjuvant and neoadjuvant chemotherapy bring potential benefits to more patients with gastric cancer based on several clinical trials. According to phase II studies and guidelines, SOX regimen as neoadjuvant chemotherapy is efficient. However, the optimal duration of neoadjuvant chemotherapy has not been established. In this study, we will evaluate the efficacy and safety of different cycles of SOX as neoadjuvant chemotherapy for patients with locally advanced gastric cancer.
RESONANCE-II trial is a prospective, multicenter, randomized, controlled phase III study which will enroll 524 patients in total. Eligible patients will be registered, pre-enrolled and receive three cycles of SOX, after which tumor response evaluations will be carried out. Those who show stable disease or progressive disease will be excluded. Patients showing complete response or partial response will be enrolled and assigned into either group A for another three cycles of SOX (six cycles in total) followed by D2 surgery; or group B for D2 surgery (three cycles in total). The primary endpoint is the rate of pathological complete response and the secondary endpoints are R0 resection rate, three-year disease-free survival, five-year overall survival, and safety.
This study is the first phase III randomized trial to compare the cycles of neoadjuvant chemotherapy using SOX for resectable locally advanced cancer. Based on a total of six to eight cycles of perioperative chemotherapy usually applied in locally advanced gastric cancer, patients in group A can be considered to have completed all perioperative chemotherapy, the results of which may suggest the feasibility of using chemotherapy only before surgery in gastric cancer.
Registered prospectively in the World Health Organization International Clinical Trials Registry Platform (WHO ICTRP) with registration number ChiCTR1900023293 on May 21st, 2019.
单纯手术治疗局部进展期胃癌较为困难。多项临床试验表明,辅助和新辅助化疗可为更多胃癌患者带来潜在获益。根据Ⅱ期研究和指南,SOX 方案作为新辅助化疗是有效的。然而,新辅助化疗的最佳周期尚未确定。本研究旨在评估不同周期 SOX 方案作为局部进展期胃癌新辅助化疗的疗效和安全性。
RESONANCE-II 试验是一项前瞻性、多中心、随机、对照的Ⅲ期研究,共纳入 524 例患者。符合条件的患者将被登记、预登记并接受 3 个周期 SOX 治疗,然后进行肿瘤反应评估。对于表现出疾病稳定或进展的患者将被排除。表现出完全缓解或部分缓解的患者将被纳入研究,并分为 A 组和 B 组。A 组患者接受另外 3 个周期 SOX(共 6 个周期)治疗,然后行 D2 手术;B 组患者直接行 D2 手术(共 3 个周期)。主要终点为病理完全缓解率,次要终点为 R0 切除率、3 年无病生存率、5 年总生存率和安全性。
本研究是首个比较 SOX 方案新辅助化疗周期用于可切除局部进展期癌症的Ⅲ期随机试验。基于局部进展期胃癌通常应用的总共 6-8 个周期的围手术期化疗,A 组患者可被认为已完成所有围手术期化疗,结果可能提示仅在术前进行化疗在胃癌中具有可行性。
于 2019 年 5 月 21 日在世界卫生组织国际临床试验注册平台(WHO ICTRP)上进行前瞻性注册,注册号为 ChiCTR1900023293。