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KRAS and extended RAS molecular profiling in metastatic colorectal cancer

机译:转移性结直肠癌的KRAS和RAS分子扩展分析

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The evolution of our understanding of the molecular biology of colorectal cancer has revolutionized our treatment paradigm. As we move into an era of genomic sequencing and tumor molecular profiling that will one day provide integral information on prognostic and predictive biomarkers, we are better able to personalize therapy accordingly, improving patient outcomes and minimizing unnecessary toxicity and cost. Progress has been made in identifying biomarkers that confer poorer outcomes with targeted therapy. KRAS exon 2 mutations have been established to be negative predictive biomarkers to anti-EGFR therapies, but more recent data support extended RAS testing that has recently been integrated into clinical practice. In this article, we review the evolution of KRAS and extended RAS testing as negative predictive biomarkers to anti-EGFR therapy, both as monotherapy and in combination with chemotherapy in advanced colorectal cancer.
机译:我们对大肠癌分子生物学理解的发展,彻底改变了我们的治疗范式。随着我们进入基因组测序和肿瘤分子谱分析的时代,有一天将提供有关预后和预测性生物标志物的完整信息,因此我们能够更好地个性化治疗,从而改善患者预后并最大程度地减少不必要的毒性和费用。在鉴定赋予靶向治疗不良结果的生物标志物方面已取得进展。 KRAS外显子2突变已被确定为抗EGFR治疗的阴性预测生物标志物,但最近的数据支持扩展的RAS测试,该测试最近已整合到临床实践中。在本文中,我们回顾了在晚期结直肠癌中作为单一疗法或与化学疗法联合使用的KRAS和扩展RAS测试作为抗EGFR治疗的阴性预测生物标志物的演变。

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