Osimertinib in patients with T790M mutation-positive, advanced non–small cell lung cancer: Long-term follow-up from a pooled analysis of 2 phase 2 studies

  • Myung Ju Ahn
  • , Chun Ming Tsai
  • , Frances A. Shepherd
  • , Lyudmila Bazhenova
  • , Lecia V. Sequist
  • , Toyoaki Hida
  • , James C.H. Yang
  • , Suresh S. Ramalingam
  • , Tetsuya Mitsudomi
  • , Pasi A. Jänne
  • , Helen Mann
  • , Mireille Cantarini
  • , Glenwood Goss

Research output: Contribution to journalArticlepeer-review

148 Scopus citations

Abstract

Background: Osimertinib is a third-generation epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor (TKI) that is selective for both EGFR-TKI–sensitizing and T790M (threonine-to-methionine substitution at codon 790)-resistance mutations. The authors present long-term follow-up data from a preplanned, pooled analysis of phase 2 studies, the AZD9291 First Time in Patients Ascending Dose Study (AURA) extension trial (clincialtrials.gov identifier NCT01802632) and the AURA2 trial (NCT02094261). Methods: Patients with centrally confirmed, T790M mutation-positive, advanced non-small cell lung cancer received osimertinib 80 mg once daily until disease progression or study discontinuation. Response was assessed by a blinded, independent, central review using Response Evaluation Criteria in Solid Tumors, version 1.1. The primary endpoint was the objective response rate. Results: In total, 411 patients received osimertinib (second line, 129 patients; third line or later, 282 patients). At the data cutoff date of November 1, 2016, the median treatment exposure was 16.4 months (range, 0-29.7 months), the objective response rate was 66% (95% confidence interval [CI], 61%-70%), the median response duration was 12.3 months (95% CI, 11.1-13.8 months), and the median progression-free survival was 9.9 months (95% CI, 9.5-12.3 months). At the data cutoff date of May 1, 2018, 271 patients (66%) had died, and 140 patients (34%) had discontinued before death. The median overall survival was 26.8 months (95% CI, 24.0-29.1 months); and the 12-month, 24-month, and 36-month survival rates were 80%, 55%, and 37%, respectively. Grade ≥3 possibly causally related (investigator assessed) adverse events were reported in 65 patients (16%), and the most common were rash (grouped terms; 42%; grade ≥3, 1%) and diarrhea (39%; <1%). Conclusions: This pooled analysis represents the most mature clinical trial data for osimertinib in patients with pretreated, T790M-positive, advanced non-small cell lung cancer, further establishing osimertinib as a standard of care for this patient population.

Original languageEnglish
Pages (from-to)892-901
Number of pages10
JournalCancer
Volume125
Issue number6
DOIs
StatePublished - 15 Mar 2019
Externally publishedYes

Keywords

  • AZD9291 First Time in Patients Ascending Dose Study (AURA)
  • epidermal growth factor receptor (EGFR)
  • osimertinib
  • pooled analysis
  • threonine-to-methionine mutation at codon 790 (T790M)
  • tyrosine kinase inhibitor (TKI)

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