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Updated: May 11, 2026

A Bioluminescent and Fluorescent Orthotopic Syngeneic Murine Model of Androgen-dependent and Castration-resistant Prostate Cancer
Published on: March 6, 2018
Perspectives on treatment of metastatic castration-resistant prostate cancer
Axel S Merseburger1, Joaquim Bellmunt, Cheryl Jenkins
1Department of Urology and Urologic Oncology, Hannover Medical School, Hannover, Germany. merseburger.axel@mh-hannover.de
Abstract:
The arrival of several new agents--cabazitaxel, abiraterone acetate, enzalutamide, and radium-223--is changing the treatment options and management of patients with metastatic castration-resistant prostate cancer (mCRPC). Many other novel agents are also being investigated. As new drugs become approved, new treatment strategies and markers to best select which patients will best respond to which drug are needed. This review article is a summary of a European Treatment Practices Meeting, which was convened to discuss these latest data on novel agents and current treatment strategies in the mCRPC setting.
Insights
New agents like cabazitaxel and abiraterone acetate are transforming metastatic castration-resistant prostate cancer (mCRPC) treatment. New strategies are needed to match patients with the best novel drugs for improved outcomes.
Area of Science:
- Oncology
- Pharmacology
Background:
- Metastatic castration-resistant prostate cancer (mCRPC) management is evolving rapidly.
- Several novel therapeutic agents are now available and under investigation.
Purpose of the Study:
- To summarize recent data on novel agents for mCRPC.
- To discuss current and future treatment strategies for mCRPC.
Main Methods:
- This review summarizes discussions from a European Treatment Practices Meeting.
- Focuses on novel agents including cabazitaxel, abiraterone acetate, enzalutamide, and radium-223.
Main Results:
- New agents are significantly altering the treatment landscape for mCRPC.
- There is a growing need for predictive biomarkers to guide treatment selection.
Conclusions:
- The advent of new drugs necessitates updated treatment paradigms in mCRPC.
- Further research is required to optimize patient selection for novel therapies.
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