Osimertinib in egfr-mutated lung cancer: A review of the existing and emerging clinical data

23Citations
Citations of this article
44Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

The use of epidermal growth factor receptor (EGFR) inhibitors such as osimerti-nib has improved outcomes and quality of life for patients with EGFR-mutated non-small cell lung cancer (NSCLC). Osimertinib has become the preferred EGFR tyrosine kinase inhibitor (TKIs) for patients with these mutations after demonstrating superior efficacy compared to first generation EGFR TKIs, such as erlotinib and gefitinib. More recently osimertinib has also shown to be beneficial in patients with resectable NSCLC harboring EGFR mutations irrespective of whether they received adjuvant chemotherapy or not. The drug is now FDA approved in this setting. With osimertinib being used more commonly in earlier stage and front-line settings, we are more likely to see patients who develop resistance to this drug. The aim of this review is to provide a comprehensive review of the data with osimertinib in EGFR mutation positive NSCLC, potential resistance mechanisms and an overview of key ongoing clinical trials.

Cite

CITATION STYLE

APA

Lee, C. S., Milone, M., & Seetharamu, N. (2021). Osimertinib in egfr-mutated lung cancer: A review of the existing and emerging clinical data. OncoTargets and Therapy, 14, 4579–4597. https://doi.org/10.2147/OTT.S227032

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free