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Results of the FLAC European Database of Metastatic Castration-Resistant Prostate Cancer Patients Treated With Docetaxel, Cabazitaxel, and Androgen Receptor-Targeted Agents.

Authors :
Angelergues A
Efstathiou E
Gyftaki R
Wysocki PJ
Lainez N
Gonzalez I
Castellano DE
Ozguroglu M
Carbonero IG
Flechon A
Borrega P
Guillot A
Balea BC
Le Moulec S
Esteban E
Munarriz J
Rubio G
Birtle AJ
Delanoy N
Bellmunt J
Oudard S
Source :
Clinical genitourinary cancer [Clin Genitourin Cancer] 2018 Aug; Vol. 16 (4), pp. e777-e784. Date of Electronic Publication: 2018 Feb 23.
Publication Year :
2018

Abstract

Background: Several agents have demonstrated an overall survival (OS) benefit in patients with metastatic castration-resistant prostate cancer (mCRPC); however, the optimal sequencing of these therapies is unknown as a result of a lack of prospective randomized controlled trials. This retrospective study aimed to identify clinical factors influencing outcomes and to determine optimal treatment sequencing in patients with mCRPC treated with cabazitaxel (CABA) and/or androgen receptor-targeted agents (ART) after androgen-deprivation therapy (ADT) and docetaxel (DOC).<br />Patients and Methods: Records of 574 consecutive patients treated (2012-2016) at 44 centers in 6 countries were retrospectively examined.<br />Results: A total of 267 patients received ADT → DOC → CABA (group 1), 183 patients ADT → DOC → ART → CABA (group 2), and 124 patients ADT → DOC → CABA → ART (group 3), with respective median OS from diagnosis of mCRPC of 38.3, 44.45, and 53.9 months (P = .012 for group 3 vs. group 1). Multivariate analysis showed response to first ADT ≤ 12 months, Gleason score of 8 to 10, clinical progression, and high prostate-specific antigen levels at mCRPC diagnosis were associated with worse OS. Prior receipt of ART did not influence activity of CABA.<br />Conclusion: OS appeared to increase with the number of life-extending therapies, with a sequence including DOC, CABA, and an ART providing the greatest OS benefit.<br /> (Copyright © 2018 Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
1938-0682
Volume :
16
Issue :
4
Database :
MEDLINE
Journal :
Clinical genitourinary cancer
Publication Type :
Academic Journal
Accession number :
29550200
Full Text :
https://doi.org/10.1016/j.clgc.2018.02.016