Alpha and Beta Radiation for Theragnostics
- PMID: 38688775
- DOI: 10.1016/j.cpet.2024.03.006
Alpha and Beta Radiation for Theragnostics
Abstract
Targeted radionuclide therapy (TRT) has significantly evolved from its beginnings with iodine-131 to employing carrier molecules with beta emitting isotopes like lutetium-177. With the success of Lu-177-DOTATATE for neuroendocrine tumors and Lu-177-PSMA-617 for prostate cancer, several other beta emitting radioisotopes, such as Cu-67 and Tb-161, are being explored for TRT. The field has also expanded into targeted alpha therapy (TAT) with agents like radium-223 for bone metastases in prostate cancer, and several other alpha emitter radioisotopes with carrier molecules, such as Ac-225, and Pb-212 under clinical trials. Despite these advancements, the scope of TRT in treating diverse solid tumors and integration with other therapies like immunotherapy remains under investigation. The success of antibody-drug conjugates further complements treatments with TRT, though challenges in treatment optimization continue.
Keywords: Actinium-225; Alpha particle; Beta particle; Lead-212; Lutetium-177; Targeted alpha therapy; Targeted radionuclide therapy; Terbium-161.
Copyright © 2024 Elsevier Inc. All rights reserved.
Conflict of interest statement
Disclosure G. Sgouros is a founder of, and holds equity in, Rapid. He serves as a member of Rapid’s Board of Directors. H. Song is a consultant for Progenics Pharmaceuticals, Inc (Lantheus). Acknowledgement George Sgouros acknowledges the funding support of National Institute of Health (P01CA272222).
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