| Literature DB >> 28151719 |
Bruce Montgomery1, Maria S Tretiakova2, Anthony M Joshua3, Martin E Gleave4, Neil Fleshner3, Glenn J Bubley5, Elahe A Mostaghel6,7, Kim N Chi8, Daniel W Lin9, Martin Sanda10, William Novotny11, Kenneth Wu11, Philip W Kantoff12,13, Brett T Marck14, Stephen Plymate14, Steven P Balk5, Peter S Nelson15,2,6,9, Alvin M Matsumoto15,14, Rosina T Lis12, Adam Kibel16, Gabriel P Haas17, Andrew Krivoshik17, Alison Hannah11, Mary-Ellen Taplin12.
Abstract
Purpose: Prostate cancer is dependent on androgen receptor (AR) activation. Optimal AR antagonism may effectively cytoreduce local disease and suppress or eliminate micrometastases. We evaluated neoadjuvant therapy prior to prostatectomy with the potent AR antagonist enzalutamide (enza) either alone or in combination with dutasteride (dut) and leuprolide (enza/dut/luteinizing hormone-releasing hormone analogues [LHRHa]).Experimental Design: Forty-eight of 52 men with intermediate or high-risk localized prostate cancer proceeded to prostatectomy after neoadjuvant enzalutamide or enza/dut/LHRHa for 6 months. We assessed pathologic complete response (pCR), minimal residual disease (MRD; ≤3 mm maximum diameter of residual disease), residual cancer burden (RCB), and expression of PSA and serum and tissue androgen concentrations. We compared the proportion of patients with pCR in each treatment arm with a historical control rate of 5%, based on previous reports of flutamide with LHRHa.Entities:
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Year: 2016 PMID: 28151719 PMCID: PMC5570479 DOI: 10.1158/1078-0432.CCR-16-1357
Source DB: PubMed Journal: Clin Cancer Res ISSN: 1078-0432 Impact factor: 12.531