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Update on third-generation EGFR tyrosine kinase inhibitors

   
@article{TLCR3317,
	author = {Jhanelle Gray and Eric Haura},
	title = {Update on third-generation EGFR tyrosine kinase inhibitors},
	journal = {Translational Lung Cancer Research},
	volume = {3},
	number = {6},
	year = {2014},
	keywords = {},
	abstract = {Among patients with non-small cell lung cancer (NSCLC), EGFR mutations, 90% of which present as an exon 19 deletion or exon 21 point mutation L858R, have been detected in Western and Asian populations at a rate of ~15% and ~40%, respectively. To date, numerous trials have established the efficacy and toxicity profile of singleagent oral EGFR-tyrosine kinase inhibitor (TKI) therapies for EGFR-TKI-naïve NSCLC patients harboring EGFR mutations. These trials include IPASS for gefitinib (1), Optimal for erlotinib (2), and LUX-Lung 3 for afatinib (3). Still, the majority of patients will eventually develop resistance.},
	issn = {2226-4477},	url = {https://tlcr.amegroups.org/article/view/3317}
}