Survival Outcomes From a Cumulative Analysis of Worldwide Observational Studies on Sequential Use of New Agents in Metastatic Castration-Resistant Prostate Cancer.
Abiraterone Acetate
/ pharmacology
Age Factors
Aged
Androgen Receptor Antagonists
/ pharmacology
Antineoplastic Combined Chemotherapy Protocols
/ pharmacology
Benzamides
Docetaxel
/ pharmacology
Humans
Kallikreins
/ blood
Kaplan-Meier Estimate
Male
Neoplasm Grading
Nitriles
Observational Studies as Topic
Phenylthiohydantoin
/ analogs & derivatives
Progression-Free Survival
Prostate
/ pathology
Prostate-Specific Antigen
/ blood
Prostatic Neoplasms, Castration-Resistant
/ blood
Retrospective Studies
Taxoids
/ pharmacology
Androgen-receptor targeting agents
Chemotherapy
Second-line
Sequencing
Third-line
Journal
Clinical genitourinary cancer
ISSN: 1938-0682
Titre abrégé: Clin Genitourin Cancer
Pays: United States
ID NLM: 101260955
Informations de publication
Date de publication:
02 2020
02 2020
Historique:
received:
19
05
2019
revised:
12
08
2019
accepted:
10
09
2019
pubmed:
27
11
2019
medline:
30
1
2021
entrez:
27
11
2019
Statut:
ppublish
Résumé
The sequential use of a number of new agents (NAs) have improved the overall survival (OS) of patients with metastatic castration-resistant prostate cancer whose disease progresses after docetaxel (DOC) treatment. The aim of this study was to assess the cumulative survival outcomes of different sequencing strategies by evaluating the individual data from published studies of patients treated with a post-DOC treatment sequence of 2 NAs. The patients' individual data were analyzed to investigate whether different sequencing strategies lead to differences in OS. We analyzed the data of 1099 evaluable patients. Among the patients treated with a second-line new hormone agent (NHA), median OS from the start of third-line treatment was significantly longer in the patients treated with cabazitaxel (CABA) than in those treated with abiraterone acetate or enzalutamide. Median cumulative OS (cumOS) from the start of second-line treatment was 21.1 months in the patients who received NHA then NHA, 22.1 months in those who received NHA then CABA, and 21.0 months in those who received CABA then NHA. Among the patients with a second-line progression-free survival of ≥6 months, median cumOS was significantly longer in patients who received CABA-including sequences than in those treated with NHA then NHA sequences (29.5 vs. 24.8 months; P = .03). Our findings suggest that the sequential use of NAs with different mechanisms of action improves cumOS regardless of the order in which they are administered, thus supporting the hypothesis of cross-resistance between the 2 NHAs.
Identifiants
pubmed: 31767448
pii: S1558-7673(19)30279-4
doi: 10.1016/j.clgc.2019.09.010
pii:
doi:
Substances chimiques
Androgen Receptor Antagonists
0
Benzamides
0
Nitriles
0
Taxoids
0
Docetaxel
15H5577CQD
Phenylthiohydantoin
2010-15-3
cabazitaxel
51F690397J
enzalutamide
93T0T9GKNU
KLK3 protein, human
EC 3.4.21.-
Kallikreins
EC 3.4.21.-
Prostate-Specific Antigen
EC 3.4.21.77
Abiraterone Acetate
EM5OCB9YJ6
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
69-76.e4Commentaires et corrections
Type : ErratumIn
Informations de copyright
Copyright © 2019. Published by Elsevier Inc.