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Mechanisms of resistance to anti-EGFR therapy in colorectal cancer

Oncotarget · 2016 · Vol. 8(3) · pp. 3980–4000
Ben ZhaoLu WangHong QiuMingsheng ZhangLi SunPing PengQianqian YuXianglin Yuan

Abstract

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.

Colorectal Cancer Treatments and StudiesLung Cancer Treatments and MutationsHER2/EGFR in Cancer ResearchMedicineColorectal cancerEpidermal growth factor receptorTargeted therapyEGFR inhibitorsAcquired resistanceCombination therapyOncologyRefractory (planetary science)Cancer

MeSH terms

CetuximabPanitumumabAntibodies, MonoclonalHumansMutationNeoplasm MetastasisColorectal NeoplasmsSignal TransductionGene Expression Regulation, Neoplasticras ProteinsDrug Resistance, NeoplasmProtein Kinase InhibitorsGene Regulatory NetworksErbB Receptors

Funding

  • National Natural Science Foundation of China
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