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Bismuth-213 for Targeted Radionuclide Therapy: From Atom to Bedside
In contrast to external high energy photon or proton therapy, targeted radionuclide therapy (TRNT) is a systemic cancer treatment allowing targeted irradiation of a primary tumor and all its metastases, resulting in less collateral damage to normal tissues. The α-emitting radionuclide bismuth-213 ((...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8143329/ https://www.ncbi.nlm.nih.gov/pubmed/33919391 http://dx.doi.org/10.3390/pharmaceutics13050599 |
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author | Ahenkorah, Stephen Cassells, Irwin Deroose, Christophe M. Cardinaels, Thomas Burgoyne, Andrew R. Bormans, Guy Ooms, Maarten Cleeren, Frederik |
author_facet | Ahenkorah, Stephen Cassells, Irwin Deroose, Christophe M. Cardinaels, Thomas Burgoyne, Andrew R. Bormans, Guy Ooms, Maarten Cleeren, Frederik |
author_sort | Ahenkorah, Stephen |
collection | PubMed |
description | In contrast to external high energy photon or proton therapy, targeted radionuclide therapy (TRNT) is a systemic cancer treatment allowing targeted irradiation of a primary tumor and all its metastases, resulting in less collateral damage to normal tissues. The α-emitting radionuclide bismuth-213 ((213)Bi) has interesting properties and can be considered as a magic bullet for TRNT. The benefits and drawbacks of targeted alpha therapy with (213)Bi are discussed in this review, covering the entire chain from radionuclide production to bedside. First, the radionuclide properties and production of (225)Ac and its daughter (213)Bi are discussed, followed by the fundamental chemical properties of bismuth. Next, an overview of available acyclic and macrocyclic bifunctional chelators for bismuth and general considerations for designing a (213)Bi-radiopharmaceutical are provided. Finally, we provide an overview of preclinical and clinical studies involving (213)Bi-radiopharmaceuticals, as well as the future perspectives of this promising cancer treatment option. |
format | Online Article Text |
id | pubmed-8143329 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-81433292021-05-25 Bismuth-213 for Targeted Radionuclide Therapy: From Atom to Bedside Ahenkorah, Stephen Cassells, Irwin Deroose, Christophe M. Cardinaels, Thomas Burgoyne, Andrew R. Bormans, Guy Ooms, Maarten Cleeren, Frederik Pharmaceutics Review In contrast to external high energy photon or proton therapy, targeted radionuclide therapy (TRNT) is a systemic cancer treatment allowing targeted irradiation of a primary tumor and all its metastases, resulting in less collateral damage to normal tissues. The α-emitting radionuclide bismuth-213 ((213)Bi) has interesting properties and can be considered as a magic bullet for TRNT. The benefits and drawbacks of targeted alpha therapy with (213)Bi are discussed in this review, covering the entire chain from radionuclide production to bedside. First, the radionuclide properties and production of (225)Ac and its daughter (213)Bi are discussed, followed by the fundamental chemical properties of bismuth. Next, an overview of available acyclic and macrocyclic bifunctional chelators for bismuth and general considerations for designing a (213)Bi-radiopharmaceutical are provided. Finally, we provide an overview of preclinical and clinical studies involving (213)Bi-radiopharmaceuticals, as well as the future perspectives of this promising cancer treatment option. MDPI 2021-04-21 /pmc/articles/PMC8143329/ /pubmed/33919391 http://dx.doi.org/10.3390/pharmaceutics13050599 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Ahenkorah, Stephen Cassells, Irwin Deroose, Christophe M. Cardinaels, Thomas Burgoyne, Andrew R. Bormans, Guy Ooms, Maarten Cleeren, Frederik Bismuth-213 for Targeted Radionuclide Therapy: From Atom to Bedside |
title | Bismuth-213 for Targeted Radionuclide Therapy: From Atom to Bedside |
title_full | Bismuth-213 for Targeted Radionuclide Therapy: From Atom to Bedside |
title_fullStr | Bismuth-213 for Targeted Radionuclide Therapy: From Atom to Bedside |
title_full_unstemmed | Bismuth-213 for Targeted Radionuclide Therapy: From Atom to Bedside |
title_short | Bismuth-213 for Targeted Radionuclide Therapy: From Atom to Bedside |
title_sort | bismuth-213 for targeted radionuclide therapy: from atom to bedside |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8143329/ https://www.ncbi.nlm.nih.gov/pubmed/33919391 http://dx.doi.org/10.3390/pharmaceutics13050599 |
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