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Updated: Jun 27, 2026

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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
Early PSA Decline Predicts Survival Outcomes in Metastatic Castration-Resistant Prostate Cancer Treated with Androgen
Engin Hendem1, Mehmet Zahid Koçak2, Oguzhan Yıldız2
1Department of Medical Oncology, Erzincan Mengücek Gazi Eğitim ve Araştırma Hastanesi, 24100 Erzincan, Turkey.
Medicina (Kaunas, Lithuania)
|June 26, 2026
Summary
A 50% prostate-specific antigen (PSA) reduction at three months indicates better outcomes for metastatic castration-resistant prostate cancer (mCRPC) patients on androgen receptor pathway inhibitors (ARPIs). Early PSA kinetics aids in risk stratification and monitoring.
Area of Science:
- Oncology
- Urology
- Pharmacology
Background:
- Metastatic castration-resistant prostate cancer (mCRPC) is heterogeneous, posing challenges in identifying patients with limited response to androgen receptor pathway inhibitors (ARPIs).
- Prostate-specific antigen (PSA) kinetics offer a potential early indicator of treatment efficacy.
- Timely identification of non-responders to ARPIs like abiraterone acetate and enzalutamide is crucial for optimizing patient management.
Purpose of the Study:
- To evaluate the prognostic value of a ≥50% PSA reduction at three months in mCRPC patients treated with ARPIs in a real-world setting.
- To determine if early PSA kinetics can predict progression-free survival (PFS) and overall survival (OS).
Main Methods:
- Retrospective single-center study including 60 mCRPC patients treated with abiraterone acetate or enzalutamide.
- Stratification based on PSA decline at three months (≥50% vs. <50%).
- Kaplan-Meier analysis for PFS and OS, with log-rank tests and Cox proportional hazards models for prognostic variable assessment.
Main Results:
- 73.3% of patients achieved a ≥50% PSA decline at three months.
- Patients with ≥50% PSA decline demonstrated significantly longer PFS and OS compared to those with <50% decline.
- Multivariate analysis confirmed early PSA decline as a significant predictor of improved survival outcomes.
Conclusions:
- A ≥50% PSA reduction by three months is a simple, clinically relevant marker for treatment response in mCRPC patients receiving ARPIs.
- Early PSA kinetics can facilitate prompt risk stratification and enhanced clinical monitoring in routine practice.
- This finding supports the use of early PSA response to guide treatment decisions and patient follow-up strategies.

