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Updated: Oct 9, 2025

A Bioluminescent and Fluorescent Orthotopic Syngeneic Murine Model of Androgen-dependent and Castration-resistant Prostate Cancer
Published on: March 6, 2018
Impact of New Systemic Therapies in Overall Survival in Non-Metastatic Castration Resistant Prostate Cancer:
Alejo Rodriguez-Vida1, Andrés Rodríguez-Alonso2, Eduardo Useros-Rodríguez3
1Medical Oncology Department, Hospital del Mar, IMIM Research Institute, Barcelona, Spain.
Abstract:
There was a high medical need for patients with non-metastatic castration-resistant prostate cancer (nmCRPC) when several next-generation anti-androgens (apalutamide, enzalutamide, and darolutamide) demonstrated clinically relevant delays in metastasis onset. However, to date, few publications have assessed the pooled effect of these treatments on overall survival (OS). We performed a systematic review and meta-analysis of all randomized, placebo-controlled studies investigating a systemic treatment in nmCRPC. Publications were identified by searching several databases on April 7, 2021. The primary objective of this analysis was to determine the OS benefit. Secondary outcomes included the relative risk (RR) of adverse events (AEs) and grade 3-4 AEs. A sensitivity analysis with simulated data was also conducted to examine the influence of the study designs on the results. Three randomized controlled studies (SPARTAN, PROSPER, ARAMIS) met our inclusion criteria. Pooled meta-analyses showed a significant benefit in OS with the active agents versus placebo (hazard ratio [HR] 0.74, 95% confidence interval [CI] 0.65-0.83), as well as increased risk of any grade (RR 1.09, 95% CI 1.01-1.17) and grade 3-4 AEs (RR 1.50, 95% CI 1.23-1.83). The sensitivity analysis with SPARTAN-like simulated populations demonstrated that when using ARAMIS statistical design, OS would be statistically significant in 98.1% of the cases, at a shorter follow-up and with lower number of events. First-line treatment of nmCRPC patients with anti-androgens increased OS with an acceptable safety profile. In light of the different study designs and follow-up, results should be interpreted separately.
Insights
Next-generation anti-androgens significantly improve overall survival for non-metastatic castration-resistant prostate cancer (nmCRPC) patients. These treatments offer a survival benefit with manageable side effects, establishing a new standard of care.
Area of Science:
- Oncology
- Clinical Pharmacology
- Biostatistics
Background:
- Non-metastatic castration-resistant prostate cancer (nmCRPC) presents a significant unmet medical need.
- Next-generation anti-androgens (apalutamide, enzalutamide, darolutamide) have shown efficacy in delaying metastasis.
- Limited data exist on the pooled impact of these agents on overall survival (OS).
Purpose of the Study:
- To conduct a systematic review and meta-analysis of randomized, placebo-controlled trials in nmCRPC.
- To determine the overall survival (OS) benefit of systemic treatments in nmCRPC.
- To assess the risk of adverse events (AEs) associated with these treatments.
Main Methods:
- Systematic review and meta-analysis of randomized, placebo-controlled studies.
- Inclusion criteria: systemic treatment for nmCRPC, placebo control.
- Databases searched up to April 7, 2021; primary outcome: OS; secondary outcomes: AE risk.
Main Results:
- Three trials (SPARTAN, PROSPER, ARAMIS) met inclusion criteria.
- Pooled analysis revealed a significant OS benefit with active agents vs. placebo (HR 0.74; 95% CI 0.65-0.83).
- Increased risk of any-grade (RR 1.09; 95% CI 1.01-1.17) and grade 3-4 AEs (RR 1.50; 95% CI 1.23-1.83) observed.
Conclusions:
- First-line treatment of nmCRPC with anti-androgens significantly increases OS.
- The safety profile of these agents is acceptable.
- Study design variations necessitate careful interpretation of individual trial results.
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