| Literature DB >> 26169963 |
Deborah Ayeni1, Katerina Politi2, Sarah B Goldberg3.
Abstract
Third-generation mutant-specific EGFR tyrosine kinase inhibitors are showing robust clinical activity, particularly in lung cancers harboring the EGFR(T790M) mutation, yet acquired resistance to these agents emerges. Additional mutations in EGFR can confer resistance that, depending on their genomic context, could determine new drug sensitivities of the cancer cells. ©2015 American Association for Cancer Research.Entities:
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Year: 2015 PMID: 26169963 PMCID: PMC4720502 DOI: 10.1158/1078-0432.CCR-15-1211
Source DB: PubMed Journal: Clin Cancer Res ISSN: 1078-0432 Impact factor: 12.531