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Updated: May 7, 2026

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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
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Retreatment of Metastatic Castration-Resistant Prostate Cancer Patients with 223Ra Therapy in Daily Practice
Joost H H M van Riel1, Maarten L Donswijk2, Christel Brouwer3
1Department of Urology, Radboud University Medical Center, Nijmegen, The Netherlands.
Summary
Radium-223 (²²³Ra) retreatment is safe and beneficial for select patients with metastatic castration-resistant prostate cancer (mCRPC) and bone metastases. This real-world study shows good tolerability and suggests retreatment improves outcomes in advanced mCRPC.
Area of Science:
- Oncology
- Radiopharmaceuticals
- Prostate Cancer Therapeutics
Background:
- Metastatic castration-resistant prostate cancer (mCRPC) with bone metastases presents significant treatment challenges.
- Radium-223 dichloride (²²³Ra) is an approved therapy, with potential for retreatment after an initial course.
Purpose of the Study:
- To evaluate the safety and efficacy of ²²³Ra retreatment in a real-world mCRPC population.
- To identify predictors of treatment completion and survival during ²²³Ra retreatment.
Main Methods:
- Multicenter, retrospective cohort study of mCRPC patients receiving ²²³Ra retreatment.
- Primary endpoint: safety (hematologic and nonhematologic adverse events).
- Secondary endpoints: injections administered, overall survival, biochemical response rates.
Main Results:
- Sixty-one patients evaluated; median age 75 years.
- ²²³Ra retreatment was well-tolerated, with no grade 4 or 5 adverse events.
- Median overall survival was 16.9 months; 56% showed ≥30% alkaline phosphatase response.
Conclusions:
- ²²³Ra retreatment is safe and potentially beneficial for selected mCRPC patients.
- High hemoglobin, prior PSA response, and no prior chemotherapy predicted retreatment completion.
- Patients with good performance status and prior PSA response may benefit most from retreatment.

