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Updated: Sep 19, 2025

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.
Background:
Metastatic castration-resistant prostate cancer (mCRPC) presents a challenge for clinicians in determining the optimal treatment sequence because of the lack of direct head-to-head comparisons, which is further complicated by the now-widespread use of androgen receptor pathway inhibitors (ARPIs) in metastatic hormone-sensitive prostate cancer (mHSPC).
Objective:
This study is a Bayesian network meta-analysis (NMA) intended to provide a comprehensive evaluation and comparison of the efficacy of mCRPC treatments across different treatment lines.
Patients And Methods:
We performed a systematic search of ClinicalTrials.gov, extracted information, assessed the risk of bias, and reconstructed missing outcomes. We performed an NMA to evaluate treatment efficacy for overall survival (OS) and progression-free survival (PFS) in first and subsequent lines. The study followed the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) NMA guidelines and was registered with PROSPERO (CRD42024499607).
Results:
The NMA included 43 trials with 33,494 patients. ARPI-based therapies, particularly in combination with poly(ADP-ribose) polymerase inhibitors, demonstrated the most significant benefits for OS and PFS in first-line mCRPC treatment, followed by chemotherapy regimens. However, ARPI re-treatment showed limited effectiveness in subsequent lines, leading to weaker OS and PFS benefits.
Conclusions:
This NMA highlights the superiority of ARPI-based therapies and chemotherapies as first-line options for mCRPC while emphasizing the need for treatment class switching after ARPI failure. To refine treatment sequencing and enable precision care, future research should integrate individual participant data to better address patient-level heterogeneity and identify biomarkers for personalized therapy.
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.
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