| Literature DB >> 24562070 |
Lawrence T Dauer1, Matthew J Williamson, John Humm, Joseph O'Donoghue, Rashid Ghani, Robert Awadallah, Jorge Carrasquillo, Neeta Pandit-Taskar, Anne-Kirsti Aksnes, Colin Biggin, Vigdis Reinton, Michael Morris, Jean St Germain.
Abstract
The majority of patients with late stage castration-resistant prostate cancer (CRPC) develop bone metastases that often result in significant bone pain. Therapeutic palliation strategies can delay or prevent skeletal complications and may prolong survival. An alpha-particle based therapy, radium-223 dichloride (²²³RaCl₂), has been developed that delivers highly localized effects in target areas and likely reduces toxicity to adjacent healthy tissue, particularly bone marrow. Radiation safety aspects were evaluated for a single comprehensive cancer center clinical phase 1, open-label, single ascending-dose study for three cohorts at 50, 100, or 200 kBq kg⁻¹ body weight. Ten patients received administrations, and six patients completed the study with 1 y follow-up. Dose rates from patients administered ²²³Ra dichloride were typically less than 2 μSv h⁻¹ MBq⁻¹ on contact and averaged 0.02 μSv h⁻¹ MBq⁻¹ at 1 m immediately following administration. Removal was primarily by fecal excretion, and whole body effective half-lives were highly dependent upon fecal compartment transfer, ranging from 2.5-11.4 d. Radium-223 is safe and straightforward to administer using conventional nuclear medicine equipment. For this clinical study, few radiation protection limitations were recommended post-therapy based on facility evaluations. Specific precautions are dependent on local regulatory authority guidance. Subsequent studies have demonstrated significantly improved overall survival and very low toxicity, suggesting that ²²³Ra may provide a new standard of care for patients with CRPC and bone metastases.Entities:
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Year: 2014 PMID: 24562070 PMCID: PMC4981573 DOI: 10.1097/HP.0b013e3182a82b37
Source DB: PubMed Journal: Health Phys ISSN: 0017-9078 Impact factor: 1.316