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Updated: Jul 5, 2026

A Bioluminescent and Fluorescent Orthotopic Syngeneic Murine Model of Androgen-dependent and Castration-resistant Prostate Cancer
Published on: March 6, 2018
Maximal androgen blockade for advanced prostate cancer
1Sunnybrook Health Sciences Centre, Division of Urology, University of Toronto, Toronto, ON, Canada. laurence.klotz@sunnybrook.ca
Maximal androgen blockade (MAB) combining castration with anti-androgens offers a modest survival benefit for advanced prostate cancer. Bicalutamide shows potential as a preferred agent in high-risk patients.
Area of Science:
- Oncology
- Pharmacology
- Molecular Biology
Background:
- Maximal androgen blockade (MAB) combines castration with anti-androgens for advanced prostate cancer.
- Anti-androgens function as androgen-receptor antagonists, inhibiting both ligand-dependent and -independent activation pathways.
- Understanding these mechanisms is crucial for optimizing prostate cancer treatment.
Purpose of the Study:
- To review the clinical evidence for MAB in advanced prostate cancer.
- To compare the efficacy of different anti-androgens within MAB regimens.
- To identify optimal treatment strategies for high-risk prostate cancer patients.
Main Methods:
- Review of approximately 30 clinical trials evaluating MAB versus monotherapy over 25 years.
- Analysis of meta-analyses assessing survival benefits of MAB.
- Examination of preclinical data and randomized trials comparing bicalutamide-based MAB with castration alone.
Main Results:
- Meta-analyses indicate an 8% mortality reduction at 5 years with MAB (flutamide/nilutamide) compared to monotherapy.
- Preclinical data and early trial results suggest bicalutamide may offer superior efficacy.
- Further data from ongoing trials are needed to confirm bicalutamide's advantage.
Conclusions:
- MAB provides a modest survival benefit in advanced prostate cancer.
- Bicalutamide-based MAB warrants consideration for high-risk patients due to potential enhanced efficacy.
- Continued research is essential to refine MAB strategies and anti-androgen selection.
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