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
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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.

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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。
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