| Literature DB >> 29110971 |
Sergio Rizzo1, Antonio Galvano1, Francesco Pantano2, Michele Iuliani2, Bruno Vincenzi2, Francesco Passiglia1, Silvia Spoto3, Giuseppe Tonini2, Viviana Bazan1, Antonio Russo4, Daniele Santini2.
Abstract
Two new drugs, the CYP17 inhibitor abiraterone acetate and the androgen receptor (AR) antagonist enzalutamide, have recently shown to prolong OS prior chemotherapy or in docetaxel treated mCRPC patients, using steroidal therapy or placebo as control group. Updated analyses underlined the role of these new agents on two prostate-specific endpoints as radiographic progression-free survival (rPFS) and time to first skeletal-related event (tSRE). On the basis of these reports, we made an indirect comparison between abiraterone and enzalutamide. We obtained a clinically but not significant difference favouring enzalutamide over abiraterone in terms of rPFS (HR 0.48, 95% CI 0.22-1.02). No significant difference was shown in term of tSRE (HR 0.99, 95% CI 0.83-1.17). In conclusion, abiraterone and enzalutamide have both demonstrated to significantly delay the bone progression resulting in similar improvements in bone-related endpoints in patients with mCRPC.Entities:
Keywords: Abiraterone; Enzalutamide; mCRPC; rPFS; tSRE
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Year: 2017 PMID: 29110971 DOI: 10.1016/j.critrevonc.2017.09.008
Source DB: PubMed Journal: Crit Rev Oncol Hematol ISSN: 1040-8428 Impact factor: 6.312