Treatment Options in BRAF-mutant Metastatic Colorectal Cancer

M. Cefalì, Maria Celeste Palmarocchi, S. Dosso
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引用次数: 5

Abstract

Treatment of BRAF-mutant colorectal cancer (CRC) traditionally represents an unmet need, mainly due to its unfavourable prognostic outlook, limited options for targeted treatment and scarce benefit from epithelial growth-factor receptor (EGFR) inhibitors. Recently, the development of BRAF V600E inhibitors has expanded the therapeutic armamentarium, although exclusive targeting of BRAF has proved to be an unsuccessful strategy due to reactivation of the mitogen-activated protein kinase pathway through multiple escape mechanisms. Combination strategies that exploit simultaneous inhibition of BRAF, EGFR and/or mitogen-activated protein/extracellular signal-regulated kinase have achieved greater success, with the BEACON CRC trial providing the first evidence for an improvement in survival with a chemotherapy-free approach in pre-treated patients with CRC, leading to regulatory approval for the combination of encorafenib and cetuximab. Subsequent research efforts attempt to build on these foundations, exploring targeted maintenance strategies and conceivably moving the combination towards the first line of therapy soon, as well as laying the foundation for the use of liquid biopsy as a guidance tool in a precision oncology approach.
braf突变的转移性结直肠癌的治疗选择
braf突变型结直肠癌(CRC)的治疗传统上是一个未满足的需求,主要是由于其预后前景不利,靶向治疗的选择有限,以及上皮生长因子受体(EGFR)抑制剂的获益很少。最近,BRAF V600E抑制剂的开发扩大了治疗范围,尽管由于有丝分裂原激活的蛋白激酶途径通过多种逃逸机制被重新激活,特异性靶向BRAF已被证明是一种不成功的策略。同时抑制BRAF、EGFR和/或丝裂原活化蛋白/细胞外信号调节激酶的联合策略已经取得了更大的成功,BEACON CRC试验提供了首个证据,证明预先治疗的CRC患者采用无化疗方法可以改善生存,从而导致监管机构批准了enorafenib和西妥昔单抗的联合治疗。随后的研究努力试图在这些基础上,探索有针对性的维持策略,并可能很快将这种组合推向一线治疗,同时为液体活检作为精确肿瘤学方法的指导工具奠定基础。
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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