Abstract

BackgroundBoth abiraterone and enzalutamide have shown to improve overall survival (OS), progression-free survival (PFS) and prostate-specific antigen (PSA) response in patients with metastatic castration-resistant prostate cancer (mCRPC) regardless of previous treatment with chemotherapy (COU-AA3011, COU-AA3022, AFFIRM3 and PREVAIL4). The data regarding the impact of these treatments in the real world setting is scarce. This study assessed the real world survival and disease outcomes in mCRPC patients in a regional health service in Victoria with the use of abiraterone and enzalutamide.MethodsThis retrospective clinical audit included 75 patients with diagnosis of mCRPC treated with either abiraterone or enzalutamide between January 1, 2014, and December 31, 2019, at Goulburn Valley Health. Patients were stratified according to the drug received, Eastern Cooperative Oncology Group (ECOG) performance status, Gleason score, burden of disease at diagnosis, presence of visceral metastases and use of previous chemotherapy. The primary end point was PSA response (defined as a reduction in the PSA level from baseline by 50% or more). The secondary outcomes were PSA PFS, radiographic PFS, and OS.ResultsThirty-seven patients received enzalutamide, and the other 38 received abiraterone. Only 20% of patients in either group had visceral metastases. 32% of patients receiving enzalutamide had a high burden of disease, compared to 53% receiving abiraterone. 38% of patients in the enzalutamide group and 53% in the abiraterone group had received prior chemotherapy. PSA response rates were higher in the enzalutamide group than abiraterone group (70.3% vs 37.8%). Both PSA and radiographic PFS were longer in the enzalutamide group than abiraterone group; 7 months vs 5 months for both end points. OS was also found to be longer in patients receiving enzalutamide; 30 months compared to only 13 months in patients receiving abiraterone.ConclusionBoth abiraterone and enzalutamide have shown to result in significant PSA response rates, as well as PFS and OS benefit in mCRPC patients in the real world setting. The difference in responses and survival benefit are probably impacted by the unbalanced burden of disease.

Highlights

  • Both abiraterone and enzalutamide are current standard of care treatments for patients with metastatic castrate-resistant prostate cancer, and are widely used in clinical practice

  • In the COU trials, abiraterone with prednisolone compared to placebo and prednisolone resulted in a progression-free survival (PFS) and overall survival (OS) benefit in metastatic castrate-resistant prostate cancer (mCRPC) patients who had prior docetaxel chemotherapy, but only a PFS benefit was demonstrated in chemotherapy naïve mCRPC patients [1, 2]

  • A total of 75 patients were divided into two groups based on whether they received abiraterone or enzalutamide, and stratified according to ECOG performance, Gleason score, burden of disease, presence of visceral metastases and use of previous systemic therapy including chemotherapy and other androgen blockade therapies (Table 1)

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Summary

Introduction

Both abiraterone and enzalutamide are current standard of care treatments for patients with metastatic castrate-resistant prostate cancer (mCRPC), and are widely used in clinical practice. Quality of life improvement has been shown in these studies with abiraterone and enzalutamide, with reduction in time to first skeletal related event and improved pain management in this group of patients This quality of life data is especially important in patients with metastatic prostate cancer, as bony metastases can be extensive and symptomatic, and can result in acute neurological sequelae such as cord compression and cauda equina syndrome. Both abiraterone and enzalutamide have shown to improve overall survival (OS), progression-free survival (PFS) and prostate-specific antigen (PSA) response in patients with metastatic castration-resistant prostate cancer (mCRPC) regardless of previous treatment with chemotherapy (COU-AA3011, COU-AA3022, AFFIRM3 and PREVAIL4). This study assessed the real world survival and disease outcomes in mCRPC patients in a regional health service in Victoria with the use of abiraterone and enzalutamide

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