A Bayesian Network Meta-analysis of Systemic Treatments for Metastatic Castration-Resistant Prostate Cancer in First-

Marie Wosny1,2, Stefanie Aeppli3, Stefanie Fischer3

  • 1School of Medicine, University of St. Gallen (HSG), St. Jakob-Strasse 21, 9000, St. Gallen, Switzerland. mariejohanna.wosny@unisg.ch.

Targeted Oncology
|June 10, 2025
PubMed
Abstract

Insights

Androgen receptor pathway inhibitors (ARPIs) and chemotherapy are top first-line treatments for metastatic castration-resistant prostate cancer (mCRPC). Switching treatment after ARPI failure is crucial for better outcomes in mCRPC patients.

Area of Science:

  • Oncology
  • Clinical Trials
  • Pharmacology

Background:

  • Metastatic castration-resistant prostate cancer (mCRPC) treatment sequencing is complex due to limited head-to-head comparisons.
  • The widespread use of androgen receptor pathway inhibitors (ARPIs) in metastatic hormone-sensitive prostate cancer (mHSPC) further complicates mCRPC treatment decisions.

Purpose of the Study:

  • To conduct a Bayesian network meta-analysis (NMA) for comprehensive efficacy evaluation of mCRPC treatments.
  • To compare treatment efficacy across various lines of therapy in mCRPC.

Main Methods:

  • Systematic literature search of ClinicalTrials.gov.
  • Bayesian network meta-analysis (NMA) for overall survival (OS) and progression-free survival (PFS).
  • Adherence to PRISMA NMA guidelines and PROSPERO registration.

Main Results:

  • Included 43 trials with 33,494 patients.
  • ARPI-based therapies, especially with PARP inhibitors, showed significant OS and PFS benefits in first-line mCRPC.
  • ARPI re-treatment had limited efficacy in subsequent lines, with reduced OS and PFS benefits.

Conclusions:

  • ARPI-based therapies and chemotherapies are superior first-line options for mCRPC.
  • Treatment class switching is necessary after ARPI failure in mCRPC.
  • Future research should focus on individual participant data and biomarkers for personalized mCRPC therapy.