New England Journal of Medicine· 2019Q1
Overall Survival with Osimertinib in Untreated, <i>EGFR</i> -Mutated Advanced NSCLC
- 2,846citations
- Q1SCImago
- 2019year
Short summary
First-line osimertinib significantly improved overall survival by 6.8 months (38.6 vs. 31.8 months) in patients with untreated, EGFR-mutated advanced non-small-cell lung cancer (NSCLC) compared to other EGFR-TKIs.
AI-generated from the title and abstract; the full text is not read.
Key points
- First-line osimertinib resulted in a median overall survival of 38.6 months versus 31.8 months for comparator EGFR-TKIs.
- The hazard ratio for death with osimertinib was 0.80 (95.05% CI, 0.64 to 1.00; P = 0.046).
- At 3 years, 28% of patients on osimertinib were still on treatment versus 9% on comparator TKIs.
- Grade 3 or higher adverse events occurred in 42% of the osimertinib group and 47% of the comparator group.
AI-generated from the title and abstract; the full text is not read.
Abstract
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 first-line osimertinib with other EGFR-TKIs in patients with EGFR mutation-positive advanced non-small-cell lung cancer (NSCLC). The trial showed longer progression-free 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.).
The authors' abstract, as published at the source. New England Journal of Medicine, 2019 · DOI ↗
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Field: Pulmonary and Respiratory Medicine
Pulmonary and Respiratory MedicineMedicine