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 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","authors":"Y. Matsubara , H. Bando , D. Kotani , Y. Kagawa , K. Harada , H. Osumi , N. Izawa , T. Kawakami , S. Boku , T. Matsumoto , M. Wakabayashi , 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; <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":"{\"title\":\"BAYONET trial: staged combination with encorafenib, binimetinib, plus cetuximab following encorafenib plus cetuximab for BRAF V600E-mutant metastatic colorectal cancer\",\"authors\":\"Y. Matsubara , H. Bando , D. Kotani , Y. Kagawa , K. Harada , H. Osumi , N. Izawa , T. Kawakami , S. Boku , T. Matsumoto , M. Wakabayashi , 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. 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BAYONET trial: staged combination with encorafenib, binimetinib, plus cetuximab following encorafenib plus cetuximab for BRAF V600E-mutant metastatic colorectal cancer
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.