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Updated: May 10, 2026

A Bioluminescent and Fluorescent Orthotopic Syngeneic Murine Model of Androgen-dependent and Castration-resistant Prostate Cancer
Published on: March 6, 2018
Overview of the latest treatments for castration-resistant prostate cancer
1Centre de Recherche, Centre Hospitalier de l'Université de Montréal, 1560 Sherbrooke East, Montréal, QC H2L 4M1, Canada.
Abstract:
Over the past few years, we have developed an increased understanding of the molecular mechanisms that underlie prostate cancer progression and castration resistance and expanded our repertoire of therapeutic options for castration-resistant prostate cancer (CRPC). Four new agents (cabazitaxel, abiraterone acetate, enzalutamide, and radium-233) have been shown to prolong overall survival in patients with CRPC in the postchemotherapy setting. Targeting the androgen receptor pathway continues to have an important role in the treatment of CRPC, with abiraterone acetate and enzalutamide being the most exciting developments. Cabazitaxel is now considered the standard-of-care second-line chemotherapy for men with metastatic CRPC (mCRPC). Bone-targeted therapy is an active area of research, with denosumab being the first bone-targeted agent able to significantly delay the appearance of bone metastases in patients with CRPC and radium-223 being the first radiopharmaceutical agent to improve survival in patients with mCRPC.
Insights
Recent advances offer new treatments for advanced prostate cancer. New therapies like abiraterone acetate and radium-223 improve survival for castration-resistant prostate cancer patients.
Area of Science:
- Oncology
- Molecular Biology
- Pharmacology
Background:
- Prostate cancer progression and castration resistance are driven by complex molecular mechanisms.
- Therapeutic options for castration-resistant prostate cancer (CRPC) have significantly expanded.
- Understanding these mechanisms is crucial for developing effective treatments.
Purpose of the Study:
- To review the recent advancements in understanding prostate cancer progression and castration resistance.
- To summarize the new therapeutic agents available for castration-resistant prostate cancer (CRPC).
- To highlight the role of androgen receptor pathway targeting and bone-targeted therapies.
Main Methods:
- Review of recent clinical trial data and scientific literature.
- Analysis of the efficacy of novel therapeutic agents in CRPC.
- Evaluation of molecular mechanisms underlying CRPC development.
Main Results:
- Four new agents (cabazitaxel, abiraterone acetate, enzalutamide, radium-223) prolong overall survival in CRPC patients.
- Abiraterone acetate and enzalutamide show significant promise in targeting the androgen receptor pathway.
- Cabazitaxel is the standard second-line chemotherapy for metastatic CRPC (mCRPC).
- Denosumab delays bone metastases, and radium-223 improves survival in mCRPC.
Conclusions:
- Targeting the androgen receptor pathway remains a key strategy in CRPC treatment.
- New bone-targeted therapies and radiopharmaceuticals offer improved outcomes for CRPC patients.
- Continued research into molecular mechanisms will drive further therapeutic innovation for advanced prostate cancer.
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