Combining enzalutamide with abiraterone, prednisone, and androgen deprivation therapy in the STAMPEDE trial

Eur Urol. 2014 Nov;66(5):799-802. doi: 10.1016/j.eururo.2014.05.038. Epub 2014 Jun 27.

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.

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