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New England Journal of Medicine· 2017Q1· Klinik çalışma

İleri Evre Ürotelyal Karsinomda İkinci Basamak Tedavi Olarak Pembrolizumab

Pembrolizumab as Second-Line Therapy for Advanced Urothelial Carcinoma

Joaquim Bellmunt, Ronald de Wit, David J. Vaughn, Yves Fradet ve diğerleri

Kısa özet

Platin bazlı tedavinin ardından ilerleyen ileri evre ürotelyal karsinom hastalarında, pembrolizumab kemoterapiye kıyasla genel sağkalımı yaklaşık 3 ay anlamlı şekilde uzatmıştır.

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

Ana noktalar

  • Pembrolizumab, ileri evre ürotelyal karsinomda ortalama genel sağkalımı 2.9 ay (10.3'e karşı 7.4 ay) iyileştirmiştir.
  • Sağkalım faydası, genel popülasyonda ve PD-L1 ekspresyonu olan hastalarda (8.0'e karşı 5.2 ay) gözlenmiştir.
  • İlerlemesiz sağkalımda pembrolizumab ve kemoterapi arasında anlamlı bir fark bulunmamıştır.
  • Pembrolizumabda ciddi (derece 3-5) tedavi ilişkili yan etki insidansı anlamlı derecede daha düşüktür (%15.0'e karşı %49.4).

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

Özet (abstract)

BACKGROUND: Patients with advanced urothelial carcinoma that progresses after platinum-based chemotherapy have a poor prognosis and limited treatment options. METHODS: In this open-label, international, phase 3 trial, we randomly assigned 542 patients with advanced urothelial cancer that recurred or progressed after platinum-based chemotherapy to receive pembrolizumab (a highly selective, humanized monoclonal IgG4κ isotype antibody against programmed death 1 [PD-1]) at a dose of 200 mg every 3 weeks or the investigator's choice of chemotherapy with paclitaxel, docetaxel, or vinflunine. The coprimary end points were overall survival and progression-free survival, which were assessed among all patients and among patients who had a tumor PD-1 ligand (PD-L1) combined positive score (the percentage of PD-L1-expressing tumor and infiltrating immune cells relative to the total number of tumor cells) of 10% or more. RESULTS: The median overall survival in the total population was 10.3 months (95% confidence interval [CI], 8.0 to 11.8) in the pembrolizumab group, as compared with 7.4 months (95% CI, 6.1 to 8.3) in the chemotherapy group (hazard ratio for death, 0.73; 95% CI, 0.59 to 0.91; P=0.002). The median overall survival among patients who had a tumor PD-L1 combined positive score of 10% or more was 8.0 months (95% CI, 5.0 to 12.3) in the pembrolizumab group, as compared with 5.2 months (95% CI, 4.0 to 7.4) in the chemotherapy group (hazard ratio, 0.57; 95% CI, 0.37 to 0.88; P=0.005). There was no significant between-group difference in the duration of progression-free survival in the total population (hazard ratio for death or disease progression, 0.98; 95% CI, 0.81 to 1.19; P=0.42) or among patients who had a tumor PD-L1 combined positive score of 10% or more (hazard ratio, 0.89; 95% CI, 0.61 to 1.28; P=0.24). Fewer treatment-related adverse events of any grade were reported in the pembrolizumab group than in the chemotherapy group (60.9% vs. 90.2%); there were also fewer events of grade 3, 4, or 5 severity reported in the pembrolizumab group than in the chemotherapy group (15.0% vs. 49.4%). CONCLUSIONS: Pembrolizumab was associated with significantly longer overall survival (by approximately 3 months) and with a lower rate of treatment-related adverse events than chemotherapy as second-line therapy for platinum-refractory advanced urothelial carcinoma. (Funded by Merck; KEYNOTE-045 ClinicalTrials.gov number, NCT02256436 .).

Yazarların özeti; kaynağından alınmıştır. New England Journal of Medicine, 2017 · DOI ↗

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