摘要
目的:本综述的目的是讨论 RAS、BRAF 和微卫星不稳定性 (MSI) 突变模式与化疗药物疗效 [伊立替康 (IRI) 与奥沙利铂 (OXA)] 之间的潜在联系,以及这如何潜在地影响化疗骨干的选择。 方法:在对研究文献进行审查后,选择在核心期刊上发表的所有相关文章进行研究。纳入标准考虑了有关感兴趣主题的相关临床和临床前研究(OXA 和 IRI 与 KRAS/BRAF 突变和 MSI 的关系)。 结果:KRAS突变抑制切除修复交叉互补组1(ERCC1)表达,使肿瘤细胞对OXA更敏感。 OPUS、COIN 和 PRIME 试验的结果支持 BRAF 突变群体由于患者数量少而没有确凿的数据。增强的 IRI 对 MSI 细胞系的细胞毒性是由于一些错配修复 (MMR) 成分参与了各种 DNA 修复过程,以及它们在维持 IRI 和 G2/M 细胞停滞的促凋亡作用中的作用。 结论:OXA和IRI是mCRC治疗不可缺少的药物,其选择必须与靶向药物一样谨慎。我们建议考虑已知基因组改变与 OXA 和 IRI 活性之间的相互作用,以个性化 mCRC 患者的化疗。
关键词: 奥沙利铂、伊立替康、结直肠癌、化疗、分子靶点、KRAS、BRAF、MSI。
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