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Impact of KRAS and BRAF gene mutations on targeted therapies in colorectal cancer.

机译:KRAS和BRAF基因突变对结直肠癌靶向治疗的影响。

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摘要

In Journal of Clinical Oncology, Price et al1 present an analysis of the predictive and prognostic impact of KRAS and BRAF gene mutations in patients with metastatic colorectal cancer. In this study, patients were randomly assigned to receive treatment with the fluorouracil prodrug capecitabine either alone or in combination with bevacizumab, a monoclonal antibody targeting the vascular endothe-lial growth factor-A (VEGF). The authors conclude that although KRAS mutations are not prognostic, patients with BRAF mutations have significantly worse survival. However, neither mutation was found to modulate outcome when bevacizumab was added to fluorouracil-based therapy. This Understanding the Pathway article provides an opportunity to gain a better understanding of the biology underlying K-Ras and B-Raf.
机译:Price等人在《临床肿瘤学杂志》上对KRAS和BRAF基因突变对转移性结直肠癌患者的预测和预后影响进行了分析。在这项研究中,患者被随机分配接受氟尿嘧啶前药卡培他滨单独治疗或与贝伐单抗联合治疗,贝伐单抗是靶向血管内皮细胞生长因子-A(VEGF)的单克隆抗体。作者得出的结论是,尽管KRAS突变不能预后,但是具有BRAF突变的患者的生存期明显较差。但是,当将贝伐单抗添加到基于氟尿嘧啶的治疗中时,没有发现任何突变可调节结果。这篇了解途径的文章提供了一个机会,可以更好地了解K-Ras和B-Raf的生物学基础。

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