A multicenter phase II trial of ramucirumab plus irinotecan for early recurrence of gastric cancer during or after adjuvant chemotherapy with docetaxel plus S-1 therapy: the RAMIEL trial (OGSG1901).

IF 6.1 1区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY
Toshifumi Yamaguchi, Ryohei Kawabata, Yusuke Akamaru, Hidekazu Hirano, Keijiro Sugimura, Yasuhiro Miyazaki, Yoshihiro Kakeji, Yosuke Kito, Takashi Nomura, Takeshi Kawakami, Masahiro Tanemura, Atsushi Takeno, Hiroyuki Okuda, Tomohiro Matsushima, Toshio Shimokawa, Yukinori Kurokawa, Shunji Endo, Narikazu Boku, Taroh Satoh
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引用次数: 0

Abstract

Background: There is currently no established chemotherapy regimen for early recurrence of pathological stage III gastric cancer (GC) following adjuvant chemotherapy with docetaxel plus S-1 (DS) after D2 gastrectomy. We aimed to evaluate the efficacy and safety of ramucirumab plus irinotecan in patients with GC who experienced early recurrence during or within 6 months after DS adjuvant chemotherapy.

Methods: This prospective, open-label, multicenter phase II trial enrolled eligible patients treated at 25 centers of the Osaka Gastrointestinal Cancer Chemotherapy Study Group in Japan. Patients received ramucirumab (8 mg/kg) and irinotecan (150 mg/m2) every 2 weeks. The primary endpoint was overall survival (OS), and secondary endpoints included progression-free survival (PFS), objective response rate (ORR), and safety. The sample size was set at 40 based on a threshold median OS of 7 months and an expected median OS of 11 months, with a one-sided alpha error of 0.05 and a power of 0.80.

Results: Between November 2019 and July 2023, 43 patients were enrolled, and 39 were included in the analysis after excluding three ineligible patients and one who did not initiate protocol treatment. The median OS was 15.9 months (95% CI: 8.8-42.0; p = 0.003). The median PFS was 5.5 months (95% CI: 3.9-8.1), and the ORR was 38.5%. Grade  ≥ 3 adverse events, including neutropenia (25.6%) and hypertension (25.6%), were observed in more than 20% of patients.

Conclusion: Ramucirumab plus irinotecan demonstrated promising efficacy and manageable toxicity in patients with early recurrence of GC following adjuvant DS therapy.

Trial registration: This study was prospectively registered in the Japan Registry of Clinical Trials (jRCTs05119071, October 6, 2019, https://jrct.niph.go.jp/latest-detail/jRCTs051190071 ).

一项多中心II期临床试验:RAMIEL试验(OGSG1901):在多西紫杉醇加S-1辅助化疗期间或之后,雷莫单抗加伊立替康治疗胃癌早期复发。
背景:对于D2胃切除术后多西紫杉醇+ S-1 (DS)辅助化疗后病理III期胃癌(GC)早期复发,目前尚无确定的化疗方案。我们的目的是评估ramucirumab联合伊立替康在DS辅助化疗期间或后6个月内早期复发的GC患者的疗效和安全性。方法:这项前瞻性、开放标签、多中心II期试验纳入了在日本大阪胃肠癌化疗研究组25个中心接受治疗的符合条件的患者。患者每2周接受拉穆单抗(8mg /kg)和伊立替康(150mg /m2)治疗。主要终点是总生存期(OS),次要终点包括无进展生存期(PFS)、客观缓解率(ORR)和安全性。根据阈值中位OS为7个月和预期中位OS为11个月,将样本量设置为40,单侧alpha误差为0.05,幂为0.80。结果:在2019年11月至2023年7月期间,纳入了43名患者,在排除了3名不符合条件的患者和1名未启动方案治疗的患者后,将39名患者纳入分析。中位OS为15.9个月(95% CI: 8.8-42.0; p = 0.003)。中位PFS为5.5个月(95% CI: 3.9-8.1), ORR为38.5%。超过20%的患者出现≥3级不良事件,包括中性粒细胞减少症(25.6%)和高血压(25.6%)。结论:Ramucirumab联合伊立替康在辅助DS治疗后早期GC复发患者中表现出良好的疗效和可控的毒性。试验注册:本研究已在日本临床试验注册中心(jRCTs05119071, 2019年10月6日,https://jrct.niph.go.jp/latest-detail/jRCTs051190071)前瞻性注册。
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来源期刊
Gastric Cancer
Gastric Cancer 医学-胃肠肝病学
CiteScore
14.70
自引率
2.70%
发文量
80
审稿时长
6-12 weeks
期刊介绍: Gastric Cancer is an esteemed global forum that focuses on various aspects of gastric cancer research, treatment, and biology worldwide. The journal promotes a diverse range of content, including original articles, case reports, short communications, and technical notes. It also welcomes Letters to the Editor discussing published articles or sharing viewpoints on gastric cancer topics. Review articles are predominantly sought after by the Editor, ensuring comprehensive coverage of the field. With a dedicated and knowledgeable editorial team, the journal is committed to providing exceptional support and ensuring high levels of author satisfaction. In fact, over 90% of published authors have expressed their intent to publish again in our esteemed journal.
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