Pharmacotherapeutic strategies for castrate-resistant prostate cancer.
Abiraterone Acetate
/ therapeutic use
Androstenes
/ administration & dosage
Antineoplastic Combined Chemotherapy Protocols
/ administration & dosage
Benzamides
Clinical Trials as Topic
Disease-Free Survival
Docetaxel
/ administration & dosage
Drug Resistance, Neoplasm
/ drug effects
Humans
Immunotherapy
/ methods
Male
Nitriles
Phenylthiohydantoin
/ administration & dosage
Prednisone
/ administration & dosage
Progression-Free Survival
Prostatic Neoplasms, Castration-Resistant
/ drug therapy
Radium
/ administration & dosage
Taxoids
/ administration & dosage
Tissue Extracts
/ administration & dosage
Prostate cancer
abiraterone Acetate
apalutamide
carbazitaxel
castration-resistant
enzalutamide
radium-223
sipuleucel-T
Journal
Expert opinion on pharmacotherapy
ISSN: 1744-7666
Titre abrégé: Expert Opin Pharmacother
Pays: England
ID NLM: 100897346
Informations de publication
Date de publication:
Aug 2020
Aug 2020
Historique:
pubmed:
30
5
2020
medline:
18
9
2020
entrez:
30
5
2020
Statut:
ppublish
Résumé
Metastatic castration-resistant prostate cancer (CRPC) is a potentially symptomatic disease with an eventual lethal outcome. Novel pharmaceutical agents are continuously studied with encouraging results in CRPC. In this perspective, the authors present established and promising pharmacotherapeutic strategies for the management of CRPC; both with and without metastases. Apart from the different treatment strategies, the authors present the relevant sequence of treatment through disease progression. Usually, docetaxel should be considered the first line treatment in mCRPC. Abiraterone acetate (AA) plus prednisone or enzalutamide (ENZ) could be alternative treatments in chemotherapy naïve patients. Sipuleucel-T has been approved for the treatment of asymptomatic or minimally symptomatic mCRPC. Ra-223 has been approved for patients with mCRPC with symptomatic bone metastases (not visceral metastases). Cabazitaxel has been approved as the second line treatment to docetaxel in mCRPC. No differences in the overall survival has been observed between sequences starting with docetaxel versus AA/ENZ. Between AA-to-ENZ and ENZ-to-AA sequence, the AA-to-ENZ sequence appeared to be more favorable than the ENZ-to-AA regarding progression-free survival but not overall survival. Carbazitaxel seemed to retain its activity regardless of the treatment sequence. Of note, ENZ and apalutamide have been approved in non-metastatic CRPC.
Identifiants
pubmed: 32469248
doi: 10.1080/14656566.2020.1767069
doi:
Substances chimiques
Androstenes
0
Benzamides
0
Nitriles
0
Taxoids
0
Tissue Extracts
0
Docetaxel
15H5577CQD
Phenylthiohydantoin
2010-15-3
cabazitaxel
51F690397J
Radium-223
8BR2SOL3L1
sipuleucel-T
8Q622VDR18
enzalutamide
93T0T9GKNU
Abiraterone Acetate
EM5OCB9YJ6
abiraterone
G819A456D0
Prednisone
VB0R961HZT
Radium
W90AYD6R3Q
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM