Osimertinib and other third-generation EGFR TKI in EGFR-mutant NSCLC patients

J. Remon, C. E. Steuer, S. S. Ramalingam, E. Felip

Résultats de recherche: Contribution à un journalArticle 'review'Revue par des pairs

185 Citations (Scopus)

Résumé

Osimertinib was the first third-generation epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor (TKI) to receive FDA and EMA approval for metastatic EGFR-mutant non-small-cell lung cancer (NSCLC) patients that have acquired the EGFR T790M resistance mutation. Clinical trials have demonstrated the efficacy of osimertinib in this patient population and clinical trials of other third-generation EGFR TKI are currently under way. Additional challenges in this patient population, such as the upfront efficacy of osimertinib, validation of T790M in liquid biopsies as a dynamic predictive marker of efficacy, along with combination with immune checkpoint inhibitors are being explored, representing an extraordinary time of development for EGFR-mutant NSCLC.

langue originaleAnglais
Pages (de - à)i20-i27
journalAnnals of Oncology
Volume29
Les DOIs
étatPublié - 1 janv. 2018
Modification externeOui

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