A. Morgenstern, C. Apostolidis, C. Kratochwil, M. Sathekge, L. Królicki, F. Bruchertseifer
2018.10.22Current Radiopharmaceuticals
tlooto Summary
This review describes methods for the production of 225Ac and its daughter nuclide 213Bi and summarizes the current clinical experience with both alpha emitters with particular focus on recent studies of targeted alpha therapy of bladder cancer, brain tu-mors, neuroendocrine tumors and prostate cancer.
Abstract
Background: Recent reports of the remarkable therapeutic efficacy of 225Ac-labeled PSMA-617 for therapy of metastatic castration-resistant prostate cancer have under-lined the clinical potential of targeted alpha therapy. Objective and Conclusion: This review describes methods for the production of 225Ac and its daughter nuclide 213Bi and summarizes the current clinical experience with both alpha emitters with particular focus on recent studies of targeted alpha therapy of bladder cancer, brain tu-mors, neuroendocrine tumors and prostate cancer.
Citation format
MORGENSTERN, A., et al. An overview of targeted alpha therapy with 225actinium and 213bismuth. Current Radiopharmaceuticals, 2018, 11: 200–208.