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Updated: Mar 12, 2026

A Bioluminescent and Fluorescent Orthotopic Syngeneic Murine Model of Androgen-dependent and Castration-resistant Prostate Cancer
Published on: March 6, 2018
Radium-223: Insight and Perspectives in Bone-metastatic Castration-resistant Prostate Cancer
Federica Eleonora Buroni1, Marco Giovanni Persico1, Francesca Pasi2
1Nuclear Medicine Unit, Department of Oncohaematology, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.
Abstract:
223Ra prolongs overall survival in symptomatic patients affected by multiple bone-metastatic castration-resistant prostatic cancer, without visceral or nodal involvement. However, many questions remain about its mechanisms of action, and its use in clinical practice is still unresolved. First of all, what is the main target of alpha-particle emission, that is, in what way does it influences the tumor microenvironment? When is the best timing in the course of the disease, extending its use to asymptomatic low-volume or even to the micrometastatic phase? What are suitable biomarkers to be employed as prognostic factors and response indicators? Which associations with other drugs and their sequence can offer the best results, and is their effect additive or synergistic? Ultimately, in the current climate of spending review, what is the optimal cost and benefit ratio regarding available treatments? In this review, we tried to answer these questions by analyzing the available scientific literature.
Insights
Radium-223 (²²³Ra) improves survival in prostate cancer patients with bone metastases. This review explores its mechanisms, optimal use, biomarkers, combination therapies, and cost-effectiveness.
Area of Science:
- Oncology
- Nuclear Medicine
- Radiopharmaceutical Therapy
Background:
- Radium-223 (²²³Ra) is approved for symptomatic, bone-metastatic castration-resistant prostate cancer (mCRPC) without visceral or nodal involvement.
- Its precise mechanisms of action and optimal clinical application remain subjects of ongoing investigation.
Purpose of the Study:
- To review the current literature addressing key questions regarding ²²³Ra therapy in mCRPC.
- To elucidate mechanisms, optimal timing, biomarker identification, combination strategies, and cost-benefit analysis of ²²³Ra.
Main Methods:
- Systematic review of published scientific literature.
- Analysis of studies focusing on ²²³Ra's efficacy, safety, and clinical utility in prostate cancer.
Main Results:
- ²²³Ra prolongs overall survival in a specific mCRPC patient population.
- Key areas for future research include understanding alpha-particle effects on the tumor microenvironment, identifying predictive biomarkers, and optimizing combination therapies.
Conclusions:
- Further research is needed to fully define ²²³Ra's role, including its optimal use in earlier disease stages and in combination with other treatments.
- Determining the most effective sequencing and potential synergistic effects with other therapies is crucial for maximizing patient benefit and cost-effectiveness.
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