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.

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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