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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
New developments in castrate-resistant prostate cancer
N Shore1, M Mason, Th M de Reijke
1Carolina Urologic Research Center, Atlantic Urology Clinics, Myrtle Beach, SC 29572, USA. nshore@gsuro.com
BJU International
|June 8, 2012
Summary
New treatments for castrate-resistant prostate cancer (CRPC) offer more options. These include immunotherapies, hormone biosynthesis inhibitors, and targeted therapies, improving the CRPC treatment landscape.
Area of Science:
- Oncology
- Urology
Background:
- Castrate-resistant prostate cancer (CRPC) is prostate cancer that progresses despite low androgen levels.
- Historically, docetaxel was the primary treatment for metastatic CRPC.
- Recent advancements have introduced new therapeutic classes for CRPC management.
Purpose of the Study:
- To review current and emerging treatment options for castrate-resistant prostate cancer.
- To discuss the mechanisms of action for novel CRPC therapeutics.
- To consider the potential role of new agents in the CRPC treatment landscape.
Main Methods:
- Review of recently approved and investigational agents for CRPC.
- Discussion of therapeutic mechanisms, including immunotherapy, hormonal manipulation, and targeted therapies.
- Analysis of ongoing Phase III clinical trials for metastatic CRPC.
Main Results:
- Sipuleucel-T (immunotherapy) approved for non-metastatic CRPC.
- Abiraterone (androgen biosynthesis inhibitor) and cabazitaxel (chemotherapy) approved for metastatic CRPC.
- Denosumab (antibody) and zoledronic acid (bisphosphonate) options for bone metastases.
- Numerous targeted therapies and immunotherapies in late-stage development.
Conclusions:
- The treatment landscape for CRPC has significantly expanded beyond traditional chemotherapy.
- Emerging therapies target androgen receptor pathways, immune responses, and specific molecular targets.
- Further research and clinical trials are evaluating the efficacy and optimal sequencing of these novel agents in CRPC management.

