Abstract

BackgroundEnzalutamide is an oral androgen receptor targeted agent that has been shown to improve survival in PREVAIL trials and has been approved for patients with chemo-naïve metastatic castration-resistant prostate cancer (CRPC). Meanwhile, flutamide is a non-steroidal oral anti-androgen that was commonly used before the approval of bicalutamide. The objective of the OCUU-CRPC study is to compare the efficacy and safety between second-line hormonal therapy of enzalutamide and flutamide as alternative anti-androgen therapy (AAT) after combined androgen blockade (CAB) therapy that included bicalutamide in patients with CRPC.MethodsA total of 100 patients with CRPC with or without distant metastases after disease progression who received CAB therapy with bicalutamide were randomly assigned at a 1:1 ratio according to distant metastases to the enzalutamide (160 mg/day, 4 × 40 mg capsules once daily) and flutamide (375 mg/day; 3 × 125 mg tablets thrice daily) groups. The primary endpoint for the drug efficacy is the response rate of prostate-specific antigen (PSA) (i.e., the ratio of patients whose PSA declined by ≥50% from baseline) at 3 months. Meanwhile, the secondary endpoints are PSA progression rate at 3 and 6 months, PSA response rate at 6 months, change in quality of life, PSA progression-free survival, and safety. The patient registration started in January 2015 and will end in March 2018, and the follow-up period is 6 months after the last patient registration. The main result will be reported in March 2019.DiscussionIn the OCUU-CRPC study, we compare the efficacy and safety of enzalutamide or alternative AAT with flutamide in participants with CRPC who were previously treated with a CAB therapy with bicalutamide. The expected results of this study will be that enzalutamide is superior to flutamide in terms of PSA response. A longer time to disease progression with enzalutamide over flutamide may translate to better overall survival. However, flutamide may be more accessible for patients owing to its lower cost than enzalutamide.Trial registrationThe OCUU-CRPC study was prospectively registered at clinicaltrials.gov (NCT02346578, January 2015) and University Hospital Medical Information Network (UMIN000016301, January 2015).

Highlights

  • Enzalutamide is an oral androgen receptor targeted agent that has been shown to improve survival in PREVAIL trials and has been approved for patients with chemo-naïve metastatic castration-resistant prostate cancer (CRPC)

  • Before the androgen receptor targeted therapy (ART) era, the treatment options for CRPC are limited, and anti-androgen therapy (AAT) with flutamide has been widely used in Japan

  • Design, and setting of the study This study aims to compare the efficacy and safety of enzalutamide or AAT with flutamide in patients with CRPC who were previously treated with combined androgen blockade (CAB) therapy with bicalutamide

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Summary

Introduction

Enzalutamide is an oral androgen receptor targeted agent that has been shown to improve survival in PREVAIL trials and has been approved for patients with chemo-naïve metastatic castration-resistant prostate cancer (CRPC). In most patients who are treated for advanced recurrent prostate cancer with androgen-deprivation therapy (ADT) that comprise a luteinizing hormone-releasing hormone (LHRH) analogue or orchiectomy with or without an anti-androgen, disease progression occurs despite effective suppression of serum testosterone. These patients are diagnosed with castration-resistant prostate cancer (CRPC). Combined androgen blockade (CAB) therapy using an LHRH analogue with an anti-androgen is superior to ADT without an anti-androgen in terms of long-term efficacy among Japanese patients with prostate cancer [3]. CAB using bicalutamide is more widely used in Japan than LHRH analogue monotherapy, and many elderly patients with localized prostate cancer are treated with CAB

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