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A Bioluminescent and Fluorescent Orthotopic Syngeneic Murine Model of Androgen-dependent and Castration-resistant Prostate Cancer
Published on: March 6, 2018
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.
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.
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