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New England Journal of Medicine· 2016Q1

EGFR T790M Pozitif Akciğer Kanserinde Osimertinib veya Platin–Pemetreksed

Osimertinib or Platinum–Pemetrexed in <i>EGFR</i> T790M–Positive Lung Cancer

Tony Mok, Yi‐Long Wu, Myung‐Ju Ahn, Marina Chiara Garassino ve diğerleri

Kısa özet

Osimertinib, prior EGFR-TKI tedavisi sonrası ilerleme gösteren T790M pozitif ileri evre küçük hücreli dışı akciğer kanseri hastalarında platin-pemetreksede kıyasla ilerlemesiz sağkalımı (10.1 aya karşı 4.4 ay) ve objektif yanıt oranını (%71'e karşı %31) anlamlı ölçüde iyileştirmiştir.

Yapay zekâ ile başlık ve abstract'tan üretildi; tam metin okunmaz.

Ana noktalar

  • Osimertinib, platin-pemetreksed tedavisine kıyasla medyan ilerlemesiz sağkalımı 10.1 aya karşı 4.4 aya uzatmıştır (HR 0.30, P<0.001).
  • Osimertinib ile objektif yanıt oranı %71 iken platin-pemetreksed ile %31'dir (OR 5.39, P<0.001).
  • Santral sinir sistemi metastazı olan hastalarda da osimertinib, platin-pemetreksed tedavisine göre daha uzun ilerlemesiz sağkalım göstermiştir (8.5 aya karşı 4.2 ay).
  • Osimertinib ile grade 3 veya daha yüksek advers olaylar, platin-pemetreksed tedavisine (%47) göre daha az sıklıkta görülmüştür (%23).

Yapay zekâ ile başlık ve abstract'tan üretildi; tam metin okunmaz.

Özet (abstract)

BACKGROUND: Osimertinib is an epidermal growth factor receptor tyrosine kinase inhibitor (EGFR-TKI) that is selective for both EGFR-TKI sensitizing and T790M resistance mutations in patients with non-small-cell lung cancer. The efficacy of osimertinib as compared with platinum-based therapy plus pemetrexed in such patients is unknown. METHODS: In this randomized, international, open-label, phase 3 trial, we assigned 419 patients with T790M-positive advanced non-small-cell lung cancer, who had disease progression after first-line EGFR-TKI therapy, in a 2:1 ratio to receive either oral osimertinib (at a dose of 80 mg once daily) or intravenous pemetrexed (500 mg per square meter of body-surface area) plus either carboplatin (target area under the curve, 5 [AUC5]) or cisplatin (75 mg per square meter) every 3 weeks for up to six cycles; maintenance pemetrexed was allowed. In all the patients, disease had progressed during receipt of first-line EGFR-TKI therapy. The primary end point was investigator-assessed progression-free survival. RESULTS: The median duration of progression-free survival was significantly longer with osimertinib than with platinum therapy plus pemetrexed (10.1 months vs. 4.4 months; hazard ratio; 0.30; 95% confidence interval [CI], 0.23 to 0.41; P<0.001). The objective response rate was significantly better with osimertinib (71%; 95% CI, 65 to 76) than with platinum therapy plus pemetrexed (31%; 95% CI, 24 to 40) (odds ratio for objective response, 5.39; 95% CI, 3.47 to 8.48; P<0.001). Among 144 patients with metastases to the central nervous system (CNS), the median duration of progression-free survival was longer among patients receiving osimertinib than among those receiving platinum therapy plus pemetrexed (8.5 months vs. 4.2 months; hazard ratio, 0.32; 95% CI, 0.21 to 0.49). The proportion of patients with adverse events of grade 3 or higher was lower with osimertinib (23%) than with platinum therapy plus pemetrexed (47%). CONCLUSIONS: Osimertinib had significantly greater efficacy than platinum therapy plus pemetrexed in patients with T790M-positive advanced non-small-cell lung cancer (including those with CNS metastases) in whom disease had progressed during first-line EGFR-TKI therapy. (Funded by AstraZeneca; AURA3 ClinicalTrials.gov number, NCT02151981 .).

Yazarların özeti; kaynağından alınmıştır. New England Journal of Medicine, 2016 · DOI ↗

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