Clinicopathological Features and Prognosis of Unresectable Colorectal Cancer With the BRAF V600E Mutation.

Cancer diagnosis & prognosis Pub Date : 2025-03-03 eCollection Date: 2025-03-01 DOI:10.21873/cdp.10432
Yukari Ono, Koji Numata, Kenta Iguchi, Mamoru Uchiyama, Masahiro Asari, Yasushi Rino, Aya Saito, Manabu Shiozawa
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Abstract

Background/aim: Patients with unresectable advanced and recurrent colorectal cancer (CRC) and the BRAF V600E mutation have poor prognosis, and conventional chemotherapy is often ineffective. This study aimed to retrospectively evaluate the clinicopathological features and prognosis of this patient population.

Patients and methods: We examined clinicopathological characteristics and treatment outcomes of 26 patients with BRAF V600E-mutated unresectable advanced and recurrent CRC treated between June 2015 and October 2022.

Results: The mean age was 63.1±14.0 years; out of 26 patients, nine (34.6%) were female, 12 (46.2%) had right-sided CRC, and eight (30.8%) had poorly differentiated or mucinous adenocarcinoma. One patient (3.8%) had a RAS mutation, and three (11.5%) had high microsatellite instability. The median overall survival (OS) was 12.0 months. The median OS for patients treated with the BEACON regimen (encorafenib plus cetuximab, with or without binimetinib) was 13.3 months, which was significantly better than that of patients treated without it (7.2 months; hazard ratio=4.180, 95% confidence interval=1.036-18.631, p=0.029). The median progression-free survival for patients treated with BEACON regimen was 6.6 months.

Conclusion: The BRAF V600E mutation was associated with poor prognosis. The BEACON regimen resulted in improved OS compared with other CRC treatment regimens.

BRAF V600E突变不可切除结直肠癌的临床病理特征及预后
背景/目的:BRAF V600E突变的晚期复发结直肠癌(CRC)不可切除患者预后较差,常规化疗往往无效。本研究旨在回顾性评估该患者群体的临床病理特征和预后。患者和方法:我们研究了2015年6月至2022年10月期间接受治疗的26例BRAF v600e突变的晚期和复发性结直肠癌患者的临床病理特征和治疗结果。结果:患者平均年龄63.1±14.0岁;26例患者中,9例(34.6%)为女性,12例(46.2%)为右侧结直肠癌,8例(30.8%)为低分化或粘液腺癌。1例(3.8%)患者有RAS突变,3例(11.5%)患者有高微卫星不稳定性。中位总生存期(OS)为12.0个月。接受BEACON方案(encorafenib +西妥昔单抗,联合或不联合binimetinib)治疗的患者的中位OS为13.3个月,显著优于未接受BEACON方案治疗的患者(7.2个月;风险比=4.180,95%可信区间=1.036-18.631,p=0.029)。接受BEACON方案治疗的患者的中位无进展生存期为6.6个月。结论:BRAF V600E突变与不良预后相关。与其他结直肠癌治疗方案相比,BEACON方案改善了OS。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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