| Literature DB >> 24289901 |
Shouki Bazarbashi1, Marwan Bachour2, Muhammad Bulbul3, Mohammed Alotaibi4, Mohamed Jaloudi5, Hassan Jaafar5, Deborah Mukherji6, Naim Farah7, Tahseen Alrubai8, Ali Shamseddine9.
Abstract
Although most patients with prostate cancer respond to initial androgen-deprivation therapy, progression to castration-resistant prostate cancer (CRPC) is almost inevitable. In 2004, the docetaxel/prednisone regimen was approved for the management of patients with metastatic CRPC, becoming the standard first-line therapy. Recent advances have also led to an unprecedented number of approved new drugs; thus, providing several treatment options for patients with metastatic CRPC. Five new drugs have received US Food and Drug Administration-approval between 2010 and 2012: sipuleucel-T, an immunotherapeutic agent; cabazitaxel, a novel microtubule inhibitor; abiraterone acetate, a new androgen biosynthesis inhibitor; enzalutamide, a novel androgen receptor inhibitor; and denosumab, a bone-targeting agent. Such drugs are either already marketed or about to be marketed in the Middle East. Data supporting the approval of each of these agents are described in this review, as are recent approaches to the treatment of metastatic CRPC.Entities:
Keywords: Abiraterone; Cabazitaxel; Castration-resistance; Denosumab; Enzalutamide; Prostate cancer; Sipuleucel-T
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Year: 2013 PMID: 24289901 DOI: 10.1016/j.critrevonc.2013.11.001
Source DB: PubMed Journal: Crit Rev Oncol Hematol ISSN: 1040-8428 Impact factor: 6.312