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

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

Research output: Contribution to journalReview articlepeer-review

189 Citations (Scopus)

Abstract

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.

Original languageEnglish
Pages (from-to)i20-i27
JournalAnnals of Oncology
Volume29
DOIs
Publication statusPublished - 1 Jan 2018
Externally publishedYes

Keywords

  • Acquired resistance
  • EGFR TKI
  • NSCLC
  • Osimertinib

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