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New England Journal of Medicine· 2013Q1

Alfa Yayıcı Radyum-223 ve Metastatik Prostat Kanserinde Sağkalım

Alpha Emitter Radium-223 and Survival in Metastatic Prostate Cancer

Chris Parker, Sten Nilsson, Daniel Heinrich, Svein Inge Helle ve diğerleri

Kısa özet

Alfa yayıcı olan ve kemik metastazlarını hedefleyen Radyum-223 diklorür, kastrasyona dirençli prostat kanseri olan erkeklerde plaseboya kıyasla genel sağkalımı %3,7 ay (14,9'a karşı 11,3 ay) anlamlı şekilde iyileştirmiştir (faz 3 deneyi, n=921).

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

Ana noktalar

  • Radyum-223, metastatik kastrasyona dirençli prostat kanseri olan erkeklerde ortalama genel sağkalımı 11,3 aydan 14,9 aya yükseltmiştir.
  • Fayda, istatistiksel olarak anlamlı bulunmuştur (risk oranı 0,70, P<0,001) ve 921 hastanın güncellenmiş analizinde gözlemlenmiştir.
  • Radyum-223 ayrıca ikincil etkinlik uç noktalarında da fayda sağlamıştır.
  • Tedavi, düşük miyelosupresyon ve daha az yan etki ile ilişkilendirilmiştir.

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

Özet (abstract)

BACKGROUND: Radium-223 dichloride (radium-223), an alpha emitter, selectively targets bone metastases with alpha particles. We assessed the efficacy and safety of radium-223 as compared with placebo, in addition to the best standard of care, in men with castration-resistant prostate cancer and bone metastases. METHODS: In our phase 3, randomized, double-blind, placebo-controlled study, we randomly assigned 921 patients who had received, were not eligible to receive, or declined docetaxel, in a 2:1 ratio, to receive six injections of radium-223 (at a dose of 50 kBq per kilogram of body weight intravenously) or matching placebo; one injection was administered every 4 weeks. In addition, all patients received the best standard of care. The primary end point was overall survival. The main secondary efficacy end points included time to the first symptomatic skeletal event and various biochemical end points. A prespecified interim analysis, conducted when 314 deaths had occurred, assessed the effect of radium-223 versus placebo on survival. An updated analysis, when 528 deaths had occurred, was performed before crossover from placebo to radium-223. RESULTS: At the interim analysis, which involved 809 patients, radium-223, as compared with placebo, significantly improved overall survival (median, 14.0 months vs. 11.2 months; hazard ratio, 0.70; 95% confidence interval [CI], 0.55 to 0.88; two-sided P=0.002). The updated analysis involving 921 patients confirmed the radium-223 survival benefit (median, 14.9 months vs. 11.3 months; hazard ratio, 0.70; 95% CI, 0.58 to 0.83; P<0.001). Assessments of all main secondary efficacy end points also showed a benefit of radium-233 as compared with placebo. Radium-223 was associated with low myelosuppression rates and fewer adverse events. CONCLUSIONS: In this study, which was terminated for efficacy at the prespecified interim analysis, radium-223 improved overall survival. (Funded by Algeta and Bayer HealthCare Pharmaceuticals; ALSYMPCA ClinicalTrials.gov number, NCT00699751.).

Yazarların özeti; kaynağından alınmıştır. New England Journal of Medicine, 2013 · DOI ↗

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