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Overall Survival with Osimertinib in Untreated, EGFR-Mutated Advanced NSCLC

  • for the FLAURA Investigators
  • Emory University
  • KU Leuven
  • Gustave Roussy Cancer Campus
  • Yonsei University
  • Moffitt Cancer Center
  • National Cancer Center Japan
  • Pulmonary Hospital of Tongji University
  • Mahidol University
  • Jilin Provincial Cancer Hospital
  • Chiang Mai University
  • Maidstone and Tunbridge Wells NHS Trust
  • Hospital Regional Universitario Carlos Haya
  • Chungbuk National University
  • University of Toronto
  • University of Parma
  • Austin Health
  • Chang Gung University
  • Osaka International Cancer Institute
  • Kansai Medical University
  • AstraZeneca
  • Université Paris-Saclay

研究成果: 期刊稿件文章同行評審

2621 引文 斯高帕斯(Scopus)

摘要

BACKGROUND Osimertinib is a third-generation, irreversible tyrosine kinase inhibitor of the epidermal growth factor receptor (EGFR-TKI) that selectively inhibits both EGFR-TKI-sensitizing and EGFR T790M resistance mutations. A phase 3 trial compared firstline osimertinib with other EGFR-TKIs in patients with EGFR mutation-positive advanced non-small-cell lung cancer (NSCLC). The trial showed longer progressionfree survival with osimertinib than with the comparator EGFR-TKIs (hazard ratio for disease progression or death, 0.46). Data from the final analysis of overall survival have not been reported. METHODS In this trial, we randomly assigned 556 patients with previously untreated advanced NSCLC with an EGFR mutation (exon 19 deletion or L858R allele) in a 1:1 ratio to receive either osimertinib (80 mg once daily) or one of two other EGFR-TKIs (gefitinib at a dose of 250 mg once daily or erlotinib at a dose of 150 mg once daily, with patients receiving these drugs combined in a single comparator group). Overall survival was a secondary end point. RESULTS The median overall survival was 38.6 months (95% confidence interval [CI], 34.5 to 41.8) in the osimertinib group and 31.8 months (95% CI, 26.6 to 36.0) in the comparator group (hazard ratio for death, 0.80; 95.05% CI, 0.64 to 1.00; P = 0.046). At 3 years, 79 of 279 patients (28%) in the osimertinib group and 26 of 277 (9%) in the comparator group were continuing to receive a trial regimen; the median exposure was 20.7 months and 11.5 months, respectively. Adverse events of grade 3 or higher were reported in 42% of the patients in the osimertinib group and in 47% of those in the comparator group. CONCLUSIONS Among patients with previously untreated advanced NSCLC with an EGFR mutation, those who received osimertinib had longer overall survival than those who received a comparator EGFR-TKI. The safety profile for osimertinib was similar to that of the comparator EGFR-TKIs, despite a longer duration of exposure in the osimertinib group. (Funded by AstraZeneca; FLAURA ClinicalTrials.gov number, NCT02296125.)

原文英語
頁(從 - 到)41-50
頁數10
期刊New England Journal of Medicine
382
發行號1
DOIs
出版狀態已出版 - 02 01 2020
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Publisher Copyright:
Copyright © 2019 Massachusetts Medical Society.

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