Osimertinib in Resected <i>EGFR</i> -Mutated Non–Small-Cell Lung Cancer
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Scores machine (provisoires)
Scores de référence d'un modèle non mature (critères de maturité non atteints, 7 itérations). Un score ordonne; il n'affirme jamais une catégorie.
Les deux têtes enseignantes du modèle étudiant, lues sur ce travail. Un score ordonne la base pour la relecture; il n'affirme jamais une catégorie, et le statut de validation accompagne chaque rangée tel quel.
- Écart entre enseignants
- 0,307 · la distance entre les deux têtes enseignantes sur ce seul travail
- Statut de validation
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Résumé
BACKGROUND: ) mutation-positive advanced non-small-cell lung cancer (NSCLC). The efficacy and safety of osimertinib as adjuvant therapy are unknown. METHODS: mutation-positive NSCLC in a 1:1 ratio to receive either osimertinib (80 mg once daily) or placebo for 3 years. The primary end point was disease-free survival among patients with stage II to IIIA disease (according to investigator assessment). The secondary end points included disease-free survival in the overall population of patients with stage IB to IIIA disease, overall survival, and safety. RESULTS: A total of 682 patients underwent randomization (339 to the osimertinib group and 343 to the placebo group). At 24 months, 90% of the patients with stage II to IIIA disease in the osimertinib group (95% confidence interval [CI], 84 to 93) and 44% of those in the placebo group (95% CI, 37 to 51) were alive and disease-free (overall hazard ratio for disease recurrence or death, 0.17; 99.06% CI, 0.11 to 0.26; P<0.001). In the overall population, 89% of the patients in the osimertinib group (95% CI, 85 to 92) and 52% of those in the placebo group (95% CI, 46 to 58) were alive and disease-free at 24 months (overall hazard ratio for disease recurrence or death, 0.20; 99.12% CI, 0.14 to 0.30; P<0.001). At 24 months, 98% of the patients in the osimertinib group (95% CI, 95 to 99) and 85% of those in the placebo group (95% CI, 80 to 89) were alive and did not have central nervous system disease (overall hazard ratio for disease recurrence or death, 0.18; 95% CI, 0.10 to 0.33). Overall survival data were immature; 29 patients died (9 in the osimertinib group and 20 in the placebo group). No new safety concerns were noted. CONCLUSIONS: mutation-positive NSCLC, disease-free survival was significantly longer among those who received osimertinib than among those who received placebo. (Funded by AstraZeneca; ADAURA ClinicalTrials.gov number, NCT02511106.).
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La notice
- Revue
- New England Journal of Medicine
- Thématique
- Lung Cancer Treatments and Mutations
- Domaine
- Medicine
- Établissements canadiens
- Princess Margaret Cancer CentreUniversity of TorontoUniversity Health Network
- Organismes subventionnaires
- Chugai PharmaceuticalEMD SeronoGenentechOno PharmaceuticalShionogiLoxo OncologyAstellas PharmaMirati TherapeuticsDaiichi Sankyo EuropeSanofiHalozymeF. Hoffmann-La RocheTaiho PharmaceuticalRegeneron PharmaceuticalsSpectrum PharmaceuticalsAmgenKyorin PharmaceuticalPfizerSymphogenAstraZenecaEli Lilly and CompanyBristol-Myers Squibb
- Mots-clés
- OsimertinibLung cancerMedicineCancer researchOncologyInternal medicineCancerEpidermal growth factor receptorErlotinib
- Résumé présent dans OpenAlex
- oui