Mechanisms of resistance to anti-EGFR therapy in colorectal cancer
Author(s) -
Ben Zhao,
Lu Wang,
Hong Qiu,
Mingsheng Zhang,
Li Sun,
Ping Peng,
Qianqian Yu,
Xianglin Yuan
Publication year - 2016
Publication title -
oncotarget
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.373
H-Index - 127
ISSN - 1949-2553
DOI - 10.18632/oncotarget.14012
Subject(s) - medicine , colorectal cancer , epidermal growth factor receptor , targeted therapy , egfr inhibitors , acquired resistance , combination therapy , oncology , refractory (planetary science) , cancer , chemotherapy , cancer research , panitumumab , bioinformatics , cetuximab , biology , astrobiology
Targeting the epidermal growth factor receptor (EGFR) either alone or in combination with chemotherapy is effective for patients with RAS wild type metastatic colorectal cancer (mCRC). However, only a small percentage of mCRC patients are sensitive to anti-EGFR therapy and even the best cases finally become refractory to this therapy. It has become apparent that the RAS mutations correlate with resistance to anti-EGFR therapy. However, these resistance mechanisms only account for nearly 35% to 50% of nonresponsive patients, suggesting that there might be additional mechanisms. In fact, several novel pathways leading to escape from anti-EGFR therapy have been reported in recent years. In this review, we provide an overview of known and novel mechanisms that contribute to both primary and acquired anti-EGFR therapy resistance, and enlist possible treatment strategies to overcome or reverse this resistance.
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