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akaturk Akademik ölçüm

Makale detayı · 2020

Osimertinib in Resected EGFR-Mutated Non\u2013Small-Cell Lung Cancer

New England Journal of Medicine

YÖKSİS OpenAlex Açık erişim · bronze SJR Q1 JCR Q1 Atıf 1795 Üst %1 Yüzdelik 100.0% FWCI 120.01
Yıl
2020
ISSN
0028-4793
Tür
article

Veri kaynağı ayrımı

  • YÖKSİS YÖKSİS makale kaydı
  • OpenAlex OpenAlex zenginleştirmesi (özet, atıf, konular)

Özet

İngilizce (OpenAlex)

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.).

Konular

  • Lung Cancer Treatments and Mutations
  • Lung Cancer Diagnosis and Treatment
  • Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis

Birincil konu Lung Cancer Treatments and Mutations

Yazarlar

  1. Yi-Long Wu
  2. Masahiro Tsuboi
  3. Jie He
  4. Thomas John
  5. Christian Grohe
  6. Margarita Majem
  7. Jonathan W. Goldman
  8. onstantin Laktionov
  9. Sang-We Kim
  10. Terufumi Kato
  11. Huu-Vinh Vu
  12. Shun Lu
  13. ADAURA Investigators
  14. ERDEM ÇUBUKÇU BURSA ULUDAĞ ÜNİVERSİTESİ