Darolutamide (ODM-201) for the treatment of prostate cancer. (13th June 2017)

• Record Type: Journal Article
• Authors: Shore, Neal D.
• Is Part Of: Expert opinion on pharmacotherapy. Volume 18:Number 9(2017)
• Page Start: 945
• Page End: 952
• Publication Date: 2017-06-13
• Subjects: Androgen receptor antagonist -- ARADES -- ARAFOR -- ODM-201 -- prostate cancer -- darolutamide; Chemotherapy -- Periodicals; 615.5805
• DOI: 10.1080/14656566.2017.1329820
• Languages: English
• ISSNs: 1465-6566

Abstract

ABSTRACT: Introduction : Androgen deprivation therapy (ADT) is a mainstay initial treatment for advanced hormone-sensitive prostate cancer (HSPC), but disease progression to castration-resistant prostate cancer (CRPC) invariably occurs when patients do not succumb to another disease or comorbidity. Recognition that the androgen receptor (AR) axis continues to drive disease progression has led to the development of several AR-directed approved agents, including abiraterone acetate and enzalutamide. An investigational agent, darolutamide (ODM-201, BAY-1841788), has completed early-phase clinical trials, and two global phase III trials are currently accruing patients. Areas covered : The unmet clinical need, pharmacokinetics, preclinical development, and clinical efficacy and safety of darolutamide for the treatment of advanced prostate cancer are reviewed. The design of two ongoing phase III trials (ARAMIS and ARASENS) of darolutamide in men with non-metastatic CRPC and metastatic HSPC, respectively, are also discussed. Expert opinion : Darolutamide is an oral, investigational, high-affinity AR antagonist which has activity against known AR mutants that confer resistance to other second-generation antiandrogens, has minimal blood–brain barrier penetration, and does not significantly increase serum testosterone. These features may offer potential advantages over the second-generation antiandrogens. In the phase I/II ARADES trial, darolutamide demonstrated promising antitumor activity and a favorable safety profile in men with metastatic CRPC.