New England Journal of Medicine· 2018Q1
Metastatik Küçük Hücreli Dışı Akciğer Kanserinde Pembrolizumab Artı Kemoterapi
Pembrolizumab plus Chemotherapy in Metastatic Non–Small-Cell Lung Cancer
- 6.647atıf
- Q1SCImago
- 2018yıl
Kısa özet
Kemoterapiye pembrolizumab eklenmesi, daha önce tedavi edilmemiş, metastatik, EGFR/ALK mutasyonu olmayan nonskuamöz KBHK hastalarında genel sağkalımı (%69,2 ila 12 ay vs. %49,4) ve progresyonsuz sağkalımı (8,8 ay vs. 4,9 ay) anlamlı şekilde iyileştirdi.
Yapay zekâ ile başlık ve abstract'tan üretildi; tam metin okunmaz.
Ana noktalar
- Pembrolizumab artı kemoterapi, metastatik KBHK'de 12 aylık genel sağkalımı %69,2'ye karşı %49,4'e (HR 0,49, P<0,001) yükseltti.
- Medyan progresyonsuz sağkalım, plasebo kombinasyonuna göre 8,8 aya (plasebo: 4,9 ay) (HR 0,52, P<0,001) ulaştı.
- Sağkalım faydaları, değerlendirilen tüm PD-L1 ifade seviyelerinde tutarlıydı.
- Derece 3 veya üzeri yan etkiler, pembrolizumab-kombinasyon (%67,2) ve plasebo-kombinasyon (%65,8) grupları arasında benzerdi.
Yapay zekâ ile başlık ve abstract'tan üretildi; tam metin okunmaz.
Özet (abstract)
BACKGROUND: First-line therapy for advanced non-small-cell lung cancer (NSCLC) that lacks targetable mutations is platinum-based chemotherapy. Among patients with a tumor proportion score for programmed death ligand 1 (PD-L1) of 50% or greater, pembrolizumab has replaced cytotoxic chemotherapy as the first-line treatment of choice. The addition of pembrolizumab to chemotherapy resulted in significantly higher rates of response and longer progression-free survival than chemotherapy alone in a phase 2 trial. METHODS: In this double-blind, phase 3 trial, we randomly assigned (in a 2:1 ratio) 616 patients with metastatic nonsquamous NSCLC without sensitizing EGFR or ALK mutations who had received no previous treatment for metastatic disease to receive pemetrexed and a platinum-based drug plus either 200 mg of pembrolizumab or placebo every 3 weeks for 4 cycles, followed by pembrolizumab or placebo for up to a total of 35 cycles plus pemetrexed maintenance therapy. Crossover to pembrolizumab monotherapy was permitted among the patients in the placebo-combination group who had verified disease progression. The primary end points were overall survival and progression-free survival, as assessed by blinded, independent central radiologic review. RESULTS: After a median follow-up of 10.5 months, the estimated rate of overall survival at 12 months was 69.2% (95% confidence interval [CI], 64.1 to 73.8) in the pembrolizumab-combination group versus 49.4% (95% CI, 42.1 to 56.2) in the placebo-combination group (hazard ratio for death, 0.49; 95% CI, 0.38 to 0.64; P<0.001). Improvement in overall survival was seen across all PD-L1 categories that were evaluated. Median progression-free survival was 8.8 months (95% CI, 7.6 to 9.2) in the pembrolizumab-combination group and 4.9 months (95% CI, 4.7 to 5.5) in the placebo-combination group (hazard ratio for disease progression or death, 0.52; 95% CI, 0.43 to 0.64; P<0.001). Adverse events of grade 3 or higher occurred in 67.2% of the patients in the pembrolizumab-combination group and in 65.8% of those in the placebo-combination group. CONCLUSIONS: In patients with previously untreated metastatic nonsquamous NSCLC without EGFR or ALK mutations, the addition of pembrolizumab to standard chemotherapy of pemetrexed and a platinum-based drug resulted in significantly longer overall survival and progression-free survival than chemotherapy alone. (Funded by Merck; KEYNOTE-189 ClinicalTrials.gov number, NCT02578680 .).
Yazarların özeti; kaynağından alınmıştır. New England Journal of Medicine, 2018 · DOI ↗
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