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Updated: Jun 20, 2026

A Bioluminescent and Fluorescent Orthotopic Syngeneic Murine Model of Androgen-dependent and Castration-resistant Prostate Cancer
Published on: March 6, 2018
Cytotoxic compounds in the treatment of castration-resistant prostate cancer
Patrick Lee1, Jeanny B Aragon-Ching
1Division of Hematology and Oncology, George Washington University Medical Center, Washington, DC 20037, USA.
Abstract:
Prostate cancer is the most common non-cutaneous cancer among men in the United States. Most will be diagnosed at an early stage, but a significant number will still develop metastatic castration resistant disease. Docetaxel has demonstrated improved quality of life and overall survival in metastatic castration-resistant prostate cancer but virtually all patients will ultimately become refractory to taxane therapy. Second-line options are limited and new effective chemotherapeutic agents or combinations are needed in this setting. This review will focus on cytotoxic compounds in clinical investigation either in combination with taxanes in the first or second-line setting and other novel compounds, such as platinums and microtubule-targeting agents that are in active clinical investigation.
Insights
New chemotherapy drugs are needed for prostate cancer that no longer responds to docetaxel. This review examines novel cytotoxic compounds, including platinums and microtubule agents, in clinical trials for advanced prostate cancer.
Area of Science:
- Oncology
- Urology
- Medical Chemistry
Background:
- Prostate cancer is a leading cancer in US men, often diagnosed early.
- Metastatic castration-resistant prostate cancer (mCRPC) develops in a significant number of patients.
- Docetaxel improves survival in mCRPC, but resistance is nearly universal.
Purpose of the Study:
- To review novel cytotoxic agents for advanced prostate cancer.
- To identify new therapeutic options beyond taxane resistance.
- To focus on compounds in clinical investigation for mCRPC.
Main Methods:
- Literature review of clinical investigations.
- Focus on cytotoxic compounds in combination therapy.
- Examination of novel agents like platinums and microtubule-targeting drugs.
Main Results:
- Taxane therapy is effective but limited by resistance.
- Second-line treatment options for mCRPC are scarce.
- Several novel compounds are under active clinical investigation.
Conclusions:
- There is a critical need for new chemotherapeutic agents in prostate cancer.
- Novel compounds, including platinums and microtubule agents, show promise.
- Ongoing clinical trials are evaluating these agents in various settings.
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