Profile of panitumumab as first-line treatment in patients with wild-type KRAS metastatic colorectal cancer

被引:7
作者
Patel, Shiven B.
Gill, David
Garrido-Laguna, Ignacio
机构
[1] Univ Utah, Dept Internal Med, Div Oncol, Salt Lake City, UT 84112 USA
[2] Univ Utah, Ctr Invest Therapeut, Huntsman Canc Inst, Salt Lake City, UT USA
来源
ONCOTARGETS AND THERAPY | 2016年 / 9卷
关键词
panitumumab; metastatic colorectal cancer; first-line; RAS; GROWTH-FACTOR RECEPTOR; FOLFIRI PLUS BEVACIZUMAB; RANDOMIZED PHASE-III; GENE COPY NUMBER; OPEN-LABEL; MONOCLONAL-ANTIBODY; RAS MUTATIONS; ABX-EGF; COMBINATION CHEMOTHERAPY; CETUXIMAB TREATMENT;
D O I
10.2147/OTT.S68558
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
Targeted therapies against EGFR, vascular endothelial growth factor, and vascular endothelial growth factor receptor have expanded treatment options for patients with metastatic colorectal cancer (mCRC). Unfortunately, biomarkers to identify patients that are most likely to derive benefit from targeted therapies in this disease are still needed. Indeed, only RAS mutations have been identified as predictive of lack of benefit from monoclonal antibodies against EGFR in patients with mCRC. Panitumumab is a fully humanized monoclonal antibody against EGFR. In this study, we review data to support the use of panitumumab in combination with a chemotherapy backbone, in the first line setting in patients with RAS wild-type mCRC. Ongoing efforts are aimed at identifying smaller subsets of patients within the RAS wild-type group that will derive the largest benefit from anti-EGFR therapy. In the meantime, treatment with anti-EGFR therapy should be reserved for patients with RAS wild-type mCRC.
引用
收藏
页码:75 / 86
页数:12
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