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多机构随机 III 期研究方案:比较不可切除或复发性胃肠胰神经内分泌肿瘤患者联合依维莫司加兰瑞肽治疗与依维莫司单药治疗的效果;日本临床肿瘤学组研究 JCOG1901(STARTER-NET 研究)。

Study protocol for a multi-institutional randomized phase III study comparing combined everolimus plus lanreotide therapy and everolimus monotherapy in patients with unresectable or recurrent gastroenteropancreatic neuroendocrine tumors; Japan Clinical Oncology Group Study JCOG1901 (STARTER-NET study).

机构信息

JCOG Data Center/Operations Office, National Cancer Center Hospital, Tokyo, Japan.

Department of Hepatobiliary and Pancreatic Oncology, National Cancer Center Hospital, Tokyo, Japan.

出版信息

Pancreatology. 2020 Sep;20(6):1183-1188. doi: 10.1016/j.pan.2020.07.010. Epub 2020 Jul 25.

Abstract

Everolimus is recognized as one of the standard drugs for the treatment of unresectable or recurrent gastroenteropancreatic neuroendocrine tumors (NET). However, recent evidence has suggested that addition of somatostatin analogs to everolimus may yield better survival outcomes as compared to everolimus alone. In April 2020, we have initiated a randomized phase III trial in Japan, to confirm the superiority of combined everolimus plus lanreotide therapy over everolimus monotherapy in patients with unresectable or recurrent gastroenteropancreatic NETs with poor prognostic factors (Ki-67 labeling index: LI 5%-20% or Ki-67 LI < 5% with diffuse liver metastases). We plan to enroll a total of 250 patients from 76 institutions over an accrual period of 5 years. The primary endpoint is progression-free survival. The key secondary endpoint is overall survival, with response rate, disease control rate, and proportion of patients with adverse events as the other secondary endpoints. This trial is registered with the Japan Registry of Clinical Trials as jRCT1031200023 [https://jrct.niph.go.jp/en-latest-detail/jRCT1031200023].

摘要

依维莫司被认为是治疗不可切除或复发性胃肠胰神经内分泌肿瘤(NET)的标准药物之一。然而,最近的证据表明,与单独使用依维莫司相比,添加生长抑素类似物可能会带来更好的生存结果。2020 年 4 月,我们在日本启动了一项随机 III 期临床试验,以确认联合依维莫司加兰瑞肽治疗与依维莫司单药治疗不可切除或复发性具有不良预后因素(Ki-67 标记指数:LI 5%-20%或 Ki-67 LI<5%且弥漫性肝转移)的胃肠胰神经内分泌肿瘤患者的优越性。我们计划在 5 年的入组期内,从 76 家机构共招募 250 名患者。主要终点是无进展生存期。关键次要终点是总生存期,次要终点还包括缓解率、疾病控制率和不良事件患者比例。该试验已在日本临床试验注册中心注册,编号为 jRCT1031200023[https://jrct.niph.go.jp/en-latest-detail/jRCT1031200023]。

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