BAYONET trial: staged combination with encorafenib, binimetinib, plus cetuximab following encorafenib plus cetuximab for BRAF V600E-mutant metastatic colorectal cancer

Y. Matsubara , H. Bando , D. Kotani , Y. Kagawa , K. Harada , H. Osumi , N. Izawa , T. Kawakami , S. Boku , T. Matsumoto , M. Wakabayashi , T. Yoshino
{"title":"BAYONET trial: staged combination with encorafenib, binimetinib, plus cetuximab following encorafenib plus cetuximab for BRAF V600E-mutant metastatic colorectal cancer","authors":"Y. Matsubara ,&nbsp;H. Bando ,&nbsp;D. Kotani ,&nbsp;Y. Kagawa ,&nbsp;K. Harada ,&nbsp;H. Osumi ,&nbsp;N. Izawa ,&nbsp;T. Kawakami ,&nbsp;S. Boku ,&nbsp;T. Matsumoto ,&nbsp;M. Wakabayashi ,&nbsp;T. Yoshino","doi":"10.1016/j.esmogo.2024.100066","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><p>While the triplet combination of encorafenib (ENCO), binimetinib (BINI), plus cetuximab (CET) yielded a higher response rate compared with the doublet combination of ENCO plus CET, no significant survival benefits of the triplet combination were observed in patients with <em>BRAF</em> V600E-mutant metastatic colorectal cancer (mCRC), according to the BEACON CRC study. Although ENCO plus CET is the standard second-line therapy, poor prognoses are expected after disease progression.</p></div><div><h3>Trial design</h3><p>BAYONET is a single-arm multicenter phase II trial designed to evaluate the efficacy and safety of staged combination with ENCO, BINI, plus CET for patients with <em>BRAF</em> V600E-mutant mCRC refractory to ENCO plus CET. The main inclusion criteria are as follows: <em>RAS</em> wild-type/<em>BRAF</em> V600E-mutant mCRC; &lt;4 weeks from the last administration of previous ENCO or CET; no administration of other systemic therapy after refractoriness to ENCO plus CET; and complete response, partial response, or ≥4 months of stable disease in the previous ENCO plus CET. The primary endpoint of this trial is the 12-week progression-free survival rate. As a translational analysis, circulating tumor DNA for next-generation sequencing using Guardant360 is collected at two time points (before and after study treatment) to investigate potential mechanisms of resistance.</p></div>","PeriodicalId":100490,"journal":{"name":"ESMO Gastrointestinal Oncology","volume":"4 ","pages":"Article 100066"},"PeriodicalIF":0.0000,"publicationDate":"2024-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S294981982400027X/pdfft?md5=b67d1599e4ccac70c939e9503027a495&pid=1-s2.0-S294981982400027X-main.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ESMO Gastrointestinal Oncology","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S294981982400027X","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Background

While the triplet combination of encorafenib (ENCO), binimetinib (BINI), plus cetuximab (CET) yielded a higher response rate compared with the doublet combination of ENCO plus CET, no significant survival benefits of the triplet combination were observed in patients with BRAF V600E-mutant metastatic colorectal cancer (mCRC), according to the BEACON CRC study. Although ENCO plus CET is the standard second-line therapy, poor prognoses are expected after disease progression.

Trial design

BAYONET is a single-arm multicenter phase II trial designed to evaluate the efficacy and safety of staged combination with ENCO, BINI, plus CET for patients with BRAF V600E-mutant mCRC refractory to ENCO plus CET. The main inclusion criteria are as follows: RAS wild-type/BRAF V600E-mutant mCRC; <4 weeks from the last administration of previous ENCO or CET; no administration of other systemic therapy after refractoriness to ENCO plus CET; and complete response, partial response, or ≥4 months of stable disease in the previous ENCO plus CET. The primary endpoint of this trial is the 12-week progression-free survival rate. As a translational analysis, circulating tumor DNA for next-generation sequencing using Guardant360 is collected at two time points (before and after study treatment) to investigate potential mechanisms of resistance.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
BAYONET 试验:继安戈非尼加西妥昔单抗治疗 BRAF V600E 突变转移性结直肠癌之后,安戈非尼、比尼美替尼加西妥昔单抗的分阶段联合治疗
背景根据BEACON CRC研究,尽管与ENCO加CET的双联疗法相比,安戈非尼(ENCO)、比尼美替尼(BINI)加西妥昔单抗(CET)的三联疗法产生了更高的应答率,但在BRAF V600E突变转移性结直肠癌(mCRC)患者中并未观察到三联疗法带来的显著生存获益。试验设计BAYONET是一项单臂多中心II期试验,旨在评估ENCO、BINI和CET分阶段联合治疗对ENCO加CET难治的BRAF V600E突变mCRC患者的疗效和安全性。主要纳入标准如下RAS野生型/BRAF V600E突变型mCRC;距上次接受ENCO或CET治疗4周;对ENCO加CET治疗难治后未接受其他系统治疗;对ENCO加CET治疗完全应答、部分应答或病情稳定≥4个月。该试验的主要终点是 12 周无进展生存率。作为一项转化分析,将在两个时间点(研究治疗前和治疗后)收集循环肿瘤 DNA,使用 Guardant360 进行下一代测序,以研究潜在的耐药机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Evaluating trastuzumab deruxtecan in patients with gastrooesophageal adenocarcinoma who are ctDNA and HER2 positive: DECIPHER PD-L1 as a response biomarker to chemotherapy plus immune checkpoint inhibitors in operable gastroesophageal adenocarcinoma: a meta-analysis of neoadjuvant clinical trials Practical management of oligometastatic gastric cancer Risk factor of severe diarrhea and enterocolitis induced by CAPOX: a retrospective multicenter study Gastrin-releasing peptide receptor expression in gastrointestinal stromal tumours
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1