Enzalutamide (Xtandi®) in addition to standard first-line therapy in men with metastatic hormone-sensitive prostate cancer (mHSPC)

Rothschedl E
Record ID 32018000360
English
Authors' results and conclusions: Recently published results from the ENZAMET trial indicate that patients with mHSPC benefit from the addition of enzalutamide to standard first-line treatment in terms of overall survival (OS) and prostate-specific antigen progression-free survival (PSA-PFS). However, the administration of enzalutamide was associated with a higher rate of serious adverse events (AEs) as compared to standard care. Due to the ongoing status of the trial, mature final and long-term data are lacking. However, due to the nature of the open-label study design, a high risk of bias is existent and will remain even with mature data. Since final OS data and health-related quality of life (HRQoL) data are not available yet, the clinical benefit for affected patients cannot be assessed. More mature data, acquired over a longer treatment duration, are required to confirm the present results.
Details
Project Status: Completed
Year Published: 2019
URL for additional information: http://eprints.aihta.at/1216/
English language abstract: An English language summary is available
Publication Type: Full HTA
Country: Austria
MeSH Terms
  • Prostatic Neoplasms
  • Therapeutics
  • Receptors, Androgen
  • Pharmacology
  • Male
  • Androgen Receptor Antagonists
Keywords
  • Enzalutamide
  • Xtandi®
  • metastatic hormone-sensitive prostate cancer (mHSPC)
  • first-line therapy
  • ENZAMET
  • androgen receptor inhibitor
Contact
Organisation Name: Ludwig Boltzmann Institute for Health Technology Assessment
Contact Address: Ludwig Boltzmann Institute for fuer Health Technology Assessment (LBI-HTA), Garnisongasse 7/rechte Stiege Mezzanin (Top 20), 1090 Vienna, Austria. Tel: +43 1 236 8119 - 0 Fax: +43 1 236 8119 - 99
Contact Name: tarquin.mittermayr@aihta.at
Contact Email: office@aihta.at
This is a bibliographic record of a published health technology assessment from a member of INAHTA or other HTA producer. No evaluation of the quality of this assessment has been made for the HTA database.