Department of Frontier Science for Cancer and Chemotherapy, Osaka University Graduate School of Medicine, Suita, Japan.
Department of Medical Oncology, Kindai University Faculty of Medicine, 377-2, Ohno-higashi, Osaka-sayama, Osaka, 589-8511, Japan.
BMC Cancer. 2022 Jul 15;22(1):773. doi: 10.1186/s12885-022-09844-2.
Although docetaxel plus S-1 adjuvant chemotherapy after gastrectomy with D2 lymphadenectomy has been a standard of treatment for stage III gastric cancer, there is no established chemotherapy for patients with recurrence during or within six months after the completion of adjuvant docetaxel plus S-1 therapy.
The OGSG 1901 trial is a prospective, open-label, multicenter, phase II trial evaluating ramucirumab plus irinotecan for gastric cancer patients with early relapse after adjuvant docetaxel plus S-1 therapy. The key eligibility criteria were: 1) histologically confirmed gastric adenocarcinoma 2) patients who were on docetaxel plus S-1 adjuvant chemotherapy after the confirmation of pathological stage III, 3) patients with early relapse, i.e., recurrence during or within 6 months after the completion of docetaxel plus S-1 therapy, and 4) patient with Eastern Cooperative Oncology Group performance status of 0-1. Irinotecan (150 mg/m, day 1) and ramucirumab (8 mg/kg, day 1) will be administered every 2 weeks. The primary endpoint is overall survival, and the secondary endpoints are overall response rate, progression-free survival, and safety. The number of patients has been set at 40 based on the threshold and expected median survival times of 7 and 11 months, respectively, with a one-sided alpha error of 0.05 and power of 0.80. The enrollment and follow-up periods are 2 and 1.5 years, respectively.
The results of this trial will indicate whether the ramucirumab with irinotecan regimen has the potential to be a recommended treatment regimen for patients with recurrence gastric cancer during or within 6 months after the completion of adjuvant docetaxel plus S-1 therapy.
This study was registered in the Japan Registry of Clinical Trials ( jRCTs05119071 , October 6, 2019).
尽管胃切除术后接受多西紫杉醇加 S-1 辅助化疗联合 D2 淋巴结清扫术已成为 III 期胃癌的标准治疗方法,但对于辅助多西紫杉醇加 S-1 治疗完成期间或之后 6 个月内复发的患者,尚无确立的化疗方法。
OGSG1901 试验是一项前瞻性、开放标签、多中心、II 期试验,评估雷莫芦单抗联合伊立替康治疗辅助多西紫杉醇加 S-1 治疗后早期复发的胃癌患者。主要入选标准为:1)组织学证实的胃腺癌;2)病理分期为 III 期后接受多西紫杉醇加 S-1 辅助化疗的患者;3)早期复发,即在多西紫杉醇加 S-1 治疗完成期间或之后 6 个月内复发的患者;4)东部肿瘤协作组体能状态 0-1 分的患者。伊立替康(150mg/m2,第 1 天)和雷莫芦单抗(8mg/kg,第 1 天)每 2 周给药 1 次。主要终点为总生存期,次要终点为总缓解率、无进展生存期和安全性。根据阈值和预期中位生存期分别为 7 个月和 11 个月,设定 40 例患者,单侧 α 错误为 0.05,功效为 0.80。入组和随访时间分别为 2 年和 1.5 年。
该试验的结果将表明雷莫芦单抗联合伊立替康方案是否有可能成为辅助多西紫杉醇加 S-1 治疗完成期间或之后 6 个月内复发的胃癌患者的推荐治疗方案。
该研究在日本临床试验注册处(jRCTs05119071,2019 年 10 月 6 日)注册。