AI Article Synopsis

  • Local advanced gastric cancer (GC) and gastro-oesophageal junction adenocarcinoma (GEJ) are difficult to treat with surgery alone, leading to the use of neoadjuvant chemotherapy (NCT), with SOX being commonly used in China.
  • * The FRUTINEOGA trial is a phase II study that plans to enroll 54 patients to evaluate the effectiveness and side effects of combining fruquintinib with SOX before surgery.
  • * This research aims to assess various outcomes like tumor remission rates and survival, while ensuring ethical approval and patient consent are secured for the study.

Article 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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10862274PMC
http://dx.doi.org/10.1136/bmjopen-2023-075696DOI Listing

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