Molecular profiling in the treatment of colorectal cancer: focus on regorafenib

被引:18
作者
Yan, Yiyi [1 ]
Grothey, Axel [1 ]
机构
[1] Mayo Clin, Dept Med Oncol, Rochester, MN 55905 USA
关键词
metastatic colon cancer; targeted therapy; molecular profiling; regorafenib; RANDOMIZED PHASE-III; RENAL-CELL CARCINOMA; WILD-TYPE KRAS; 1ST-LINE TREATMENT; RAS MUTATIONS; BRAF MUTATION; COLON-CANCER; ANTI-PD-L1; ANTIBODY; CLINICAL ACTIVITY; DOSE-ESCALATION;
D O I
10.2147/OTT.S79145
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Metastatic colorectal cancer (mCRC) is a highly heterogeneous disease. Its treatment outcome has been significantly improved over the last decade with the incorporation of biological targeted therapies, including anti-EGFR antibodies, cetuximab and panitumumab, and VEGF inhibitors, bevacizumab, ramucirumab, and aflibercept. The identification of predictive biomarkers has further improved the survival by accurately selecting patients who are most likely to benefit from these treatments, such as RAS mutation profiling for EGFR antibodies. Regorafenib is a multikinase inhibitor currently used as late line therapy for mCRC. The molecular and genetic markers associated with regorafenib treatment response are yet to be characterized. Here, we review currently available clinical evidence of mCRC molecular profiling, such as RAS, BRAF, and MMR testing, and its role in targeted therapies with special focus on regorafenib treatment.
引用
收藏
页码:2949 / 2957
页数:9
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