Ophthalmic Toxicities in BEACON Triplet Therapy for BRAF V600E-Mutant Colorectal Cancer: A Case Series.

IF 1.5 Q4 GASTROENTEROLOGY & HEPATOLOGY
Journal of the Anus Rectum and Colon Pub Date : 2025-10-25 eCollection Date: 2025-01-01 DOI:10.23922/jarc.2025-031
Hayato Nakamura, Kiyoshi Suzumura, Kazuhiro Oiwa, Tomonori Tsuchiya, Kazumi Nishimae, Masahiro Tanaka, Masaki Terasaki, Yoshichika Okamoto
{"title":"Ophthalmic Toxicities in BEACON Triplet Therapy for BRAF V600E-Mutant Colorectal Cancer: A Case Series.","authors":"Hayato Nakamura, Kiyoshi Suzumura, Kazuhiro Oiwa, Tomonori Tsuchiya, Kazumi Nishimae, Masahiro Tanaka, Masaki Terasaki, Yoshichika Okamoto","doi":"10.23922/jarc.2025-031","DOIUrl":null,"url":null,"abstract":"<p><p>The BEACON regimen, comprising cetuximab, encorafenib, and binimetinib, is a critical treatment for BRAF-mutant metastatic colorectal cancer (mCRC). While effective, this regimen may be associated with a high frequency of serous retinal detachment (SRD) as an ocular toxicity, which is a less recognized risk in colorectal cancer. Here, we report three patients with mCRC who developed SRD shortly after starting BEACON therapy. Each patient experienced acute visual disturbances, and optical coherence tomography (OCT) confirmed SRD without other retinal abnormalities. Temporary discontinuation of therapy improved the OCT findings in all patients. Two patients resumed treatment with a doublet regimen (excluding binimetinib) and maintained stable vision without irreversible damage. The third patient continued binimetinib with an adjusted dosing schedule of 1 week administration and 1 week off, with no ocular toxicity; the other two drugs were continued. None of the patients experienced permanent vision impairment. These cases highlight the importance of early recognition and proactive management of ocular toxicity in patients receiving BEACON therapy. Regular ophthalmological monitoring and appropriate dose adjustments are essential to prevent visual damage while maintaining treatment efficacy.</p>","PeriodicalId":56349,"journal":{"name":"Journal of the Anus Rectum and Colon","volume":"9 4","pages":"465-471"},"PeriodicalIF":1.5000,"publicationDate":"2025-10-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12574812/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of the Anus Rectum and Colon","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.23922/jarc.2025-031","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"Q4","JCRName":"GASTROENTEROLOGY & HEPATOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

The BEACON regimen, comprising cetuximab, encorafenib, and binimetinib, is a critical treatment for BRAF-mutant metastatic colorectal cancer (mCRC). While effective, this regimen may be associated with a high frequency of serous retinal detachment (SRD) as an ocular toxicity, which is a less recognized risk in colorectal cancer. Here, we report three patients with mCRC who developed SRD shortly after starting BEACON therapy. Each patient experienced acute visual disturbances, and optical coherence tomography (OCT) confirmed SRD without other retinal abnormalities. Temporary discontinuation of therapy improved the OCT findings in all patients. Two patients resumed treatment with a doublet regimen (excluding binimetinib) and maintained stable vision without irreversible damage. The third patient continued binimetinib with an adjusted dosing schedule of 1 week administration and 1 week off, with no ocular toxicity; the other two drugs were continued. None of the patients experienced permanent vision impairment. These cases highlight the importance of early recognition and proactive management of ocular toxicity in patients receiving BEACON therapy. Regular ophthalmological monitoring and appropriate dose adjustments are essential to prevent visual damage while maintaining treatment efficacy.

Abstract Image

Abstract Image

Abstract Image

BRAF v600e突变型结直肠癌的BEACON三联疗法的眼部毒性:一个病例系列
BEACON方案包括西妥昔单抗、恩可非尼和比尼美替尼,是braf突变性转移性结直肠癌(mCRC)的关键治疗方案。虽然有效,但该方案可能与浆液性视网膜脱离(SRD)的高频率相关,这是一种眼毒性,在结直肠癌中较少被认识到的风险。在这里,我们报告了3例mCRC患者在开始BEACON治疗后不久发生SRD。每位患者均有急性视力障碍,光学相干断层扫描(OCT)证实SRD无其他视网膜异常。暂时停止治疗改善了所有患者的OCT表现。2例患者恢复双药治疗(不含比尼美替尼),视力稳定,无不可逆损伤。第三例患者继续服用比尼美替尼,调整给药1周,停药1周,无眼部毒性;另外两种药继续服用。没有患者出现永久性视力障碍。这些病例强调了在接受BEACON治疗的患者中早期识别和积极管理眼毒性的重要性。定期眼科监测和适当的剂量调整是必要的,以防止视力损害,同时保持治疗效果。
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 求助全文
来源期刊
Journal of the Anus Rectum and Colon
Journal of the Anus Rectum and Colon GASTROENTEROLOGY & HEPATOLOGY-
自引率
7.10%
发文量
37
审稿时长
18 weeks
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书