Targeted Radiopharmaceutical Therapy for Bone Metastases.
Journal
Seminars in nuclear medicine
ISSN: 1558-4623
Titre abrégé: Semin Nucl Med
Pays: United States
ID NLM: 1264464
Informations de publication
Date de publication:
26 Jun 2024
26 Jun 2024
Historique:
received:
16
05
2024
accepted:
22
05
2024
medline:
28
6
2024
pubmed:
28
6
2024
entrez:
27
6
2024
Statut:
aheadofprint
Résumé
Radiopharmaceutical approaches for targeting bone metastasis have traditionally focused on palliation of pain. Several agents have been clinically used over the last several decades and have proven value in pain palliation providing pain relief and improving quality of life. The role is well established across several malignancies, most commonly used in osteoblastic prostate cancer patients. These agents have primarily based on targeting and uptake in bone matrix and have mostly included beta emitting isotopes. The advent alpha emitter and FDA approval of 223Ra-dichloride has created a paradigm shift in clinical approach from application for pain palliation to treatment of bone metastasis. The approval of 223Ra-dichloride given the survival benefit in metastatic prostate cancer patients, led to predominant use of this alpha emitter in prostate cancer patients. With rapid development of radiopharmaceutical therapies and approval of other targeted agents such as 177Lu-PSMA the approach to treatment of bone metastasis has further evolved and combination treatments have increasingly been applied. Novel approaches are needed to improve and expand the use of such therapies for treatment of bone metastasis. Combination therapies with different targeting mechanisms, combining chemotherapies and cocktail of alpha and beta emitters need further exploration.
Identifiants
pubmed: 38937221
pii: S0001-2998(24)00047-3
doi: 10.1053/j.semnuclmed.2024.05.006
pii:
doi:
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Informations de copyright
Copyright © 2024. Published by Elsevier Inc.
Déclaration de conflit d'intérêts
Declaration of competing interest The authors declare the following financial interests/personal relationships that could be considered as potential competing interests: Neeta Pandit-Taskar reports honoraria from Actinium Pharmaceuticals; consulting or advisory role for innervate, Telix, and Lantheus; Speakers' Bureau association for Actinium Pharmaceuticals and Telix; research funding (institutional) from Bayer Health, Bristol Myers Squibb, Clarity Pharmaceuticals, Cellectar Biosciences, Imaginab, Janssen, Regeneron, Ymabs, and Innervate; and travel support from AstraZeneca. Other authors report no competing interest- financial interests or personal relationship.