KRAS and extended RAS molecular profiling in metastatic colorectal cancer

被引:1
|
作者
Lai, Sueyi [1 ]
Kachhela, Jaydeep [1 ]
Marshall, John L. [1 ]
机构
[1] Georgetown Univ, Med Ctr, Lombardi Comprehens Canc Ctr, 3800 Reservoir Rd NW, Washington, DC 20007 USA
关键词
cetuximab; EGFR; irinotecan; KRAS; metastatic colorectal; cancer; oxaliplatin; panitumumab; RAS;
D O I
10.2217/CRC.14.41
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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.
引用
收藏
页码:491 / 499
页数:9
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