Abstract
There are compelling reasons to study the addition of both enzalutamide and abiraterone, in combination, to standard-of-care for hormone-naïve prostate cancer. Through a protocol amendment, this will be assessed in the STAMPEDE trial, with overall survival as primary outcome measure.
Trial registration:
ClinicalTrials.gov NCT00268476.
Copyright © 2014 European Association of Urology. Published by Elsevier B.V. All rights reserved.
Publication types
-
Editorial
-
Multicenter Study
-
Randomized Controlled Trial
-
Research Support, Non-U.S. Gov't
MeSH terms
-
Androgen Antagonists / administration & dosage
-
Androstenes / administration & dosage
-
Antineoplastic Combined Chemotherapy Protocols / adverse effects
-
Antineoplastic Combined Chemotherapy Protocols / therapeutic use*
-
Benzamides
-
Cytochrome P-450 Enzyme Inhibitors / administration & dosage
-
Humans
-
Male
-
Neoplasms, Hormone-Dependent / drug therapy*
-
Neoplasms, Hormone-Dependent / metabolism
-
Neoplasms, Hormone-Dependent / pathology
-
Nitriles
-
Phenylthiohydantoin / administration & dosage
-
Phenylthiohydantoin / analogs & derivatives
-
Prednisone / administration & dosage
-
Prostatic Neoplasms / drug therapy*
-
Prostatic Neoplasms / metabolism
-
Prostatic Neoplasms / pathology
-
Research Design
-
Steroid 17-alpha-Hydroxylase / antagonists & inhibitors
-
Steroid 17-alpha-Hydroxylase / metabolism
-
Switzerland
-
Treatment Outcome
-
United Kingdom
Substances
-
Androgen Antagonists
-
Androstenes
-
Benzamides
-
Cytochrome P-450 Enzyme Inhibitors
-
Nitriles
-
Phenylthiohydantoin
-
enzalutamide
-
CYP17A1 protein, human
-
Steroid 17-alpha-Hydroxylase
-
abiraterone
-
Prednisone
Associated data
-
ClinicalTrials.gov/NCT00268476