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呋喹替尼联合奥沙利铂加 S-1(SOX)作为局部晚期胃癌(GC)或胃食管结合部腺癌(GEJ)的新辅助治疗:一项多中心、II 期、单臂、开放标签的临床研究(FRUTINEOGA)方案。

Fruquintinib plus oxaliplatin combined with S-1 (SOX) as neoadjuvant therapy for locally advanced gastric cancer (GC) or gastro-oesophageal junction adenocarcinoma (GEJ): a multicentre, phase II, single-arm, open-label clinical trial (FRUTINEOGA) protocol.

机构信息

Guangxi Medical University Cancer Hospital, Nanning, Guangxi, China.

Guangxi Medical University Cancer Hospital, Nanning, Guangxi, China

出版信息

BMJ Open. 2024 Feb 10;14(2):e075696. doi: 10.1136/bmjopen-2023-075696.

Abstract

INTRODUCTION

Curing locally advanced gastric cancer (GC) or gastro-oesophageal junction adenocarcinoma (GEJ) with surgery alone is challenging. Neoadjuvant chemotherapy (NCT) has become the standard treatment for patients with locally advanced GC/GEJ, and SOX is the most common neoadjuvant regimen in China. The generally good tolerability in patients and fruquintinib's low potential for drug-drug interaction suggest that it may be highly suitable for combinations with other antineoplastic therapies. A combination of fruquintinib, S-1 and oxaliplatin can be a promising neoadjuvant treatment for locally advanced GC/GEJ. In this phase II study, we aim to investigate the efficacy and toxicity of fruquintinib plus SOX as neoadjuvant treatment for locally advanced GC/GEJ.

METHODS AND ANALYSIS

The FRUTINEOGA trial is a prospective, multicentre, phase II, single-arm, open-label clinical trial that will enrol 54 patients. Eligible patients will be registered, enrolled and receive 2-4 cycles of fruquintinib plus SOX, after which surgery will be performed and tumour regression will be evaluated. The primary endpoint is the pathological remission rate, and the secondary endpoints are disease-free survival, overall survival, objective response rate, major pathological response rate and R0 resection rate.

ETHICS AND DISSEMINATION

Written informed consent will be required from all patients enrolled, and it will be provided by them. The study protocol received approval from the independent ethical review committee of Guangxi Medical University Cancer Hospital, Wuming Hospital of Guangxi Medical University and Wuzhou Red Cross Hospital, Wuzhou Gongren Hospital (approval number: CS2021(96)). We will submit the finalised paper for publication on completing the analyses. This study will provide valuable insights to clinicians regarding the safety and efficacy of incorporating fruquintinib into SOX as neoadjuvant treatment for locally advanced GC/GEJ. The findings have the potential to inform future research proposals and may guide the use of fruquintinib in the neoadjuvant setting for locally advanced GC/GEJ.

TRIAL REGISTRATION NUMBER

NCT05122091.

摘要

简介

单独手术治疗局部晚期胃癌(GC)或胃食管结合部腺癌(GEJ)具有挑战性。新辅助化疗(NCT)已成为局部晚期 GC/GEJ 患者的标准治疗方法,SOX 是中国最常用的新辅助方案。患者普遍能良好耐受,且呋喹替尼药物相互作用的潜在风险低,这表明其可能非常适合与其他抗肿瘤疗法联合应用。呋喹替尼、替吉奥和奥沙利铂联合治疗可能是局部晚期 GC/GEJ 的一种很有前途的新辅助治疗方法。在这项 II 期研究中,我们旨在研究呋喹替尼联合 SOX 作为局部晚期 GC/GEJ 新辅助治疗的疗效和毒性。

方法和分析

FRUTINEOGA 试验是一项前瞻性、多中心、II 期、单臂、开放标签的临床试验,将纳入 54 例患者。符合条件的患者将登记、入组并接受 2-4 周期的呋喹替尼联合 SOX 治疗,然后进行手术并评估肿瘤退缩情况。主要终点是病理缓解率,次要终点是无病生存期、总生存期、客观缓解率、主要病理缓解率和 R0 切除率。

伦理和传播

所有入组的患者都将需要签署书面知情同意书,并由他们提供。该研究方案获得了广西医科大学附属肿瘤医院、广西医科大学武鸣医院和梧州市红十字会医院、梧州市工人医院的独立伦理审查委员会的批准(批准号:CS2021(96))。我们将在完成分析后提交最终论文进行发表。本研究将为临床医生提供关于将呋喹替尼纳入 SOX 作为局部晚期 GC/GEJ 新辅助治疗的安全性和有效性的宝贵见解。研究结果有可能为未来的研究提案提供信息,并可能指导呋喹替尼在局部晚期 GC/GEJ 的新辅助治疗中的应用。

试验注册号

NCT05122091。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21be/10862274/658f43017e29/bmjopen-2023-075696f01.jpg

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