epocrates logo
epocrates logo
epocrates logo
  • 0

Journal Article Synopsis

N Engl J Med

ASCO 2024: Osimertinib for unresectable late-stage, EGFR-mutant NSCLC

June 4, 2024

card-image

Among patients with unresectable stage III EGFR-mutated NSCLC, osimertinib led to significantly longer progression-free survival (PFS) than placebo.

In the phase 3 LAURA trial, investigators randomly assigned patients with unresectable EGFR-mutated stage III NSCLC without progression during or after chemoradiotherapy to receive osimertinib or placebo until disease progression occurred or regimen was discontinued.

A total of 216 patients who’d undergone chemoradiotherapy were randomly assigned to receive osimertinib (n = 143) or placebo (n = 73). A significant PFS benefit was seen with omisertinib compared with placebo: median PFS was 39.1 months with osimertinib vs. 5.6 months with placebo (hazard ratio [HR] for disease progression or death, 0.16; 95% confidence interval [CI], 0.10-0.24; P<0.001). Percentage of patients who were alive and progression free at 12 months was 74% with osimertinib and 22% with placebo. Interim overall survival (OS) data (maturity, 20%) showed 36-month OS among 84% of osimertinib recipients vs. 74% with placebo (HR for death, 0.81; 95% CI, 0.42-1.56; P = 0.53). Incidence of grade 3+ adverse events was 35% in the osimertinib group vs. 12% in the placebo group, with radiation pneumonitis (mostly grade 1 to 2) reported in 48% and 38%, respectively. No new safety signals were reported.

Source:

Lu S, et al. (2024, June 2). N Engl J Med. Osimertinib after Chemoradiotherapy in Stage III EGFR-Mutated NSCLC. https://pubmed.ncbi.nlm.nih.gov/38828946/

learn more about epocrates plus

Clinical FAQs

Check out the answers to frequently asked questions about our clinical content.

Download Epocrates from the App StoreDownload Epocrates from the Play Store
About UsFeaturesBusiness SolutionsHelp & FeedbackCookie Preferences
© 2026 epocrates, Inc.   Terms of UsePrivacy PolicyEditorial PolicyDo Not Sell or Share My Information