Alpha and Beta Radiation for Theragnostics.
Actinium-225
Alpha particle
Beta particle
Lead-212
Lutetium-177
Targeted alpha therapy
Targeted radionuclide therapy
Terbium-161
Journal
PET clinics
ISSN: 1879-9809
Titre abrégé: PET Clin
Pays: United States
ID NLM: 101260152
Informations de publication
Date de publication:
29 Apr 2024
29 Apr 2024
Historique:
medline:
1
5
2024
pubmed:
1
5
2024
entrez:
30
4
2024
Statut:
aheadofprint
Résumé
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.
Identifiants
pubmed: 38688775
pii: S1556-8598(24)00021-X
doi: 10.1016/j.cpet.2024.03.006
pii:
doi:
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Informations de copyright
Copyright © 2024 Elsevier Inc. All rights reserved.
Déclaration de conflit d'intérêts
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).