WJOG18524G:一项评估bemarituzumab联合ramucirumab和紫杉醇治疗成纤维细胞生长因子受体2b (FGFR2b)阳性晚期胃癌或胃食管结癌(RAINBIRD)的单臂II期研究

K. Shimozaki , K. Hirata , H. Hayashi , Y. Sato , Y. Komatsu , S. Taniguchi , N. Takahashi , K. Yamaguchi , M. Furuta , T. Kawakami , Y. Narita , T. Ando , A. Makiyama , S. Mitani , T. Ogata , N. Takegawa , W. Okamoto , T. Nishina , M. Komoda , A. Hosokawa , K. Muro
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引用次数: 0

摘要

成纤维细胞生长因子受体2b (FGFR2)过表达的晚期胃癌(AGC)与不良预后和有限的治疗选择相关。Bemarituzumab选择性结合FGFR2b,正在研究与化疗联合作为一线治疗。双重抑制血管内皮生长因子-血管内皮生长因子受体和FGF-FGFR通路可能通过协同抑制血管生成和肿瘤增殖的下游信号来改善fgfr2b阳性AGC的存活。WJOG18524G试验(RAINBIRD)是一项单组、多中心II期试验,旨在评估bemarituzumab联合紫杉醇+ ramucirumab治疗fgfr2b阳性AGC患者的安全性和有效性,这些患者对一线氟嘧啶化疗不耐受或难治。主要入选标准为不可切除或转移性fgfr2b阳性胃腺癌、对氟嘧啶类化疗的难治性或不耐受、可测量的病变和0或1的功能状态。主要终点是客观缓解率,通过盲法独立中心评价来评估。转化研究计划通过在多个时间点收集肿瘤DNA (plesssion - neo)和循环肿瘤DNA (Guardant360)测序,探索贝马里单抗耐药的预测性生物标志物和机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
WJOG18524G: a single-arm phase II study evaluating bemarituzumab combined with ramucirumab and paclitaxel in fibroblast growth factor receptor 2b (FGFR2b)-positive advanced gastric or gastroesophageal junction cancer (RAINBIRD)

Background

Fibroblast growth factor receptor 2b (FGFR2)-overexpressing advanced gastric cancer (AGC) is associated with poor prognosis and limited treatment options. Bemarituzumab, which selectively binds to FGFR2b, is being investigated in combination with chemotherapy as a first-line treatment. Dual inhibition of the vascular endothelial growth factor–vascular endothelial growth factor receptor and FGF–FGFR pathways may improve the survival of FGFR2b-positive AGC through synergistic inhibition of angiogenesis and the downstream signals for tumor proliferation.

Design

The WJOG18524G trial (RAINBIRD) is a single-arm, multicenter phase II trial to evaluate the safety and efficacy of bemarituzumab in combination with paclitaxel plus ramucirumab in patients with FGFR2b-positive AGC who are intolerant or refractory to first-line fluoropyrimidine-based chemotherapy. The main inclusion criteria are unresectable or metastatic FGFR2b-positive gastric adenocarcinoma, refractoriness or intolerance to fluoropyrimidine-based chemotherapy, measurable lesions, and performance status of 0 or 1. The primary endpoint is the objective response rate, which is assessed by a blinded independent central review. Translational research is planned to explore the predictive biomarkers and mechanisms of resistance to bemarituzumab by sequencing tumor DNA (PleSSiSion-Neo) and circulating tumor DNA (Guardant360), which are collected at multiple time points.
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