A multicentre analysis of abiraterone acetate in Canadian patients with metastatic castration-resistant prostate cancer - Abstract

INTRODUCTON: The COU-AA-301 trial showed that abiraterone acetate (abiraterone), an oral cytochrome p450 CYP17 inhibitor, improved survival for men with metastatic castration-resistant prostate cancer (mCRPC) progressing after docetaxel.

To better understand the non-clinical trial experience with abiraterone, we undertook a multicentre retrospective analysis of Canadian mCRPC patients treated with abiraterone.

METHODS: Consecutive patients with mCRPC who received abiraterone post-docetaxel were identified using centralized pharmacy records. These patients came from 5 Canadian tertiary cancer centres. Patients who received abiraterone for approved indications were included. Demographics, prognostic factors, treatment outcomes and adverse events were abstracted.

RESULTS: We included 187 patients who initiated abiraterone between January 2011 and June 2012. The median age at diagnosis and abiraterone start was 65 and 73 years, respectively. Seventy-three (39%) patients had metastatic disease at diagnosis. The Eastern Cooperative Oncology Group (ECOG) performance status of 0, 1, 2 and 3 was noted in 17, 96, 39 and 8 patients, respectively. The median prostate-specific antigen (PSA) at abiraterone start was 132, with a median PSA doubling time of 2.8 months. The median follow-up of patients still on active follow-up was 13 months. The proportion of patients achieving a ≥50% PSA reduction was 64/177 (36%). PSA progression-free survival was 3.5 months (95% confidence interval [CI], 3.0, 4.0). Median overall survival from start of abiraterone was 11 months (95% CI, 8.0, 13) and 38 months (95% CI, 31, 41) from date of mCRPC. Anemia and fatigue were the most commonly reported adverse events.

CONCLUSIONS: This study carries the inherent limitations of a retrospective chart review. The outcomes in this series of men treated with abiraterone in a non-trial setting were expected, considering previous clinical trials. Our results, therefore, support the generalizability of the COU-AA-301 study results.

Written by:
Clayton R, Wu J, Heng DY, North SA, Emmenegger U, Hotte S, Chi K, Zielinski R, Al-Shamsi H, Chen L, Eigl B.   Are you the author?
Tom Baker Cancer Centre, Calgary, AB; Cross Cancer Institute, Edmonton, AB; Odette Cancer Centre, Toronto, ON; Juravinski Cancer Centre, Hamilton, ON; BC Cancer Agency, Vancouver, BC.

Reference: Can Urol Assoc J. 2014 Sep;8(9-10):E583-90.
doi: 10.5489/cuaj.1891


PubMed Abstract
PMID: 25295126

UroToday.com mCRPC Treatment Section