Novel therapeutics in metastatic colorectal cancer: molecular insights and pharmacogenomic implications

被引:8
作者
Hanna, Diana L. [1 ,2 ]
Lenz, Heinz-Josef [1 ]
机构
[1] Univ Southern Calif, Norris Comprehens Canc Ctr, Div Med Oncol, Keck Sch Med, 1441 Eastlake Ave,Suite 3456, Los Angeles, CA 90033 USA
[2] Hoag Family Canc Inst, Newport Beach, CA USA
关键词
Angiogenesis; biomarker; EGFR; fluoropyrimidines; immunotherapy; metastatic colorectal cancer; microsatellite instability; pharmacogenetics; RAF; RAS; TRIPLE ANGIOKINASE INHIBITOR; WILD-TYPE KRAS; FOLFIRI PLUS BEVACIZUMAB; EARLY TUMOR SHRINKAGE; DISEASE-FREE INTERVAL; I DOSE-ESCALATION; COLON-CANCER; PHASE-I; GROWTH-FACTOR; BIBF; 1120;
D O I
10.1586/17512433.2016.1172961
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Although the survival of metastatic colorectal cancer (mCRC) patients has improved five-fold over the last century, CRC remains a significant global health burden. Impressive strides have been made in identifying new regimens, employing maintenance strategies to limit treatment toxicities, and combining multidisciplinary approaches to achieve cure in oligometastatic disease. Attempts at personalized integration of targeted agents have been limited by the ability to identify molecularly enriched patient populations most likely to benefit. In this review, we discuss novel therapeutics and regimens recently approved and in development for mCRC. In addition, we discuss using older agents in novel combination and maintenance strategies, and highlight evidence for implementing pharmacogenomic data and non-invasive monitoring into the personalized management of mCRC patients.
引用
收藏
页码:1091 / 1108
页数:18
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