Alpha Emitter Radium-223 and Survival in Metastatic Prostate Cancer

Chris Parker(San Antonio College), Sten Nilsson(San Antonio College), Daniel Heinrich(San Antonio College), Svein Inge Helle(San Antonio College), Joe M. O’Sullivan(San Antonio College), Sophie D. Fosså(San Antonio College), Aleš Chodacki(San Antonio College), Paweł Wiechno(San Antonio College), John Logue(San Antonio College), M. Seke(San Antonio College), Anders Widmark(San Antonio College), Dag Clement Johannessen(San Antonio College), Peter Hoskin(San Antonio College), David Bottomley(San Antonio College), Nicholas D. James(San Antonio College), A. Solberg(San Antonio College), Isabel Syndikus(San Antonio College), J. Kliment(San Antonio College), Saskia Wedel(San Antonio College), S. Boehmer(San Antonio College), Marcos F. Dall’Oglio(San Antonio College), Lars Franzén(San Antonio College), Robert E. Coleman(San Antonio College), Nicholas J. Vogelzang(San Antonio College), C. Gillies O'Bryan-Tear(San Antonio College), K. Staudacher(San Antonio College), J. Garcia‐Vargas(San Antonio College), Minghua Shan(San Antonio College), Øyvind S. Bruland(San Antonio College), Oliver Sartor(San Antonio College)
New England Journal of Medicine
July 17, 2013
Cited by 3,326

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.).


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