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Radiation Dosimetry of Theragnostic Pairs for Isotopes of Iodine in IAZA

Theragnostic pairs of isotopes are used to infer radiation dosimetry for a therapeutic radiopharmaceutical from a diagnostic imaging study with the same tracer molecule labelled with an isotope better suited for the imaging task. We describe the transfer of radiation dosimetry from the diagnostic ra...

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Autores principales: Jans, Hans-S., Stypinski, Daria, Kumar, Piyush, Mercer, John R., McQuarrie, Stephen A., McEwan, Alexander J. B., Wiebe, Leonard I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9416730/
https://www.ncbi.nlm.nih.gov/pubmed/36015281
http://dx.doi.org/10.3390/pharmaceutics14081655
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author Jans, Hans-S.
Stypinski, Daria
Kumar, Piyush
Mercer, John R.
McQuarrie, Stephen A.
McEwan, Alexander J. B.
Wiebe, Leonard I.
author_facet Jans, Hans-S.
Stypinski, Daria
Kumar, Piyush
Mercer, John R.
McQuarrie, Stephen A.
McEwan, Alexander J. B.
Wiebe, Leonard I.
author_sort Jans, Hans-S.
collection PubMed
description Theragnostic pairs of isotopes are used to infer radiation dosimetry for a therapeutic radiopharmaceutical from a diagnostic imaging study with the same tracer molecule labelled with an isotope better suited for the imaging task. We describe the transfer of radiation dosimetry from the diagnostic radioiodine isotope (123)I, labelled for the hypoxia tracer molecule iodoazomycin arabinoside ([(123)I]IAZA), to isotopes (131)I (therapeutic) and (124)I (PET imaging). Uncertainties introduced by the dissimilar isotope half-lives are discussed in detail. Radioisotope dosimetries for [(123)I]IAZA were obtained previously. These data are used here to calculate residence times for (131)I and (124)I and their uncertainties. We distinguish two cases when extrapolating to infinity: purely physical decay (case A) and physical decay plus biological washout (case B). Organ doses were calculated using the MIRD schema with the OLIDNA/EXM code. Significant increases in some organ doses (in mSv per injected activity) were found for (131)I and (124)I. The most affected organs were the intestinal walls, thyroid, and urinary bladder wall. Uncertainty remained similar to (123)I for case A but considerably greater for case B, especially for long biological half-lives (GI tract). Normal tissue dosimetries for IAZA must be considered carefully when substituting isotope species. A long biological half-life can significantly increase dosimetric uncertainties. These findings are relevant when considering PET imaging studies with [(124)I]IAZA or therapeutic administration of [(131)I]IAZA.
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spelling pubmed-94167302022-08-27 Radiation Dosimetry of Theragnostic Pairs for Isotopes of Iodine in IAZA Jans, Hans-S. Stypinski, Daria Kumar, Piyush Mercer, John R. McQuarrie, Stephen A. McEwan, Alexander J. B. Wiebe, Leonard I. Pharmaceutics Communication Theragnostic pairs of isotopes are used to infer radiation dosimetry for a therapeutic radiopharmaceutical from a diagnostic imaging study with the same tracer molecule labelled with an isotope better suited for the imaging task. We describe the transfer of radiation dosimetry from the diagnostic radioiodine isotope (123)I, labelled for the hypoxia tracer molecule iodoazomycin arabinoside ([(123)I]IAZA), to isotopes (131)I (therapeutic) and (124)I (PET imaging). Uncertainties introduced by the dissimilar isotope half-lives are discussed in detail. Radioisotope dosimetries for [(123)I]IAZA were obtained previously. These data are used here to calculate residence times for (131)I and (124)I and their uncertainties. We distinguish two cases when extrapolating to infinity: purely physical decay (case A) and physical decay plus biological washout (case B). Organ doses were calculated using the MIRD schema with the OLIDNA/EXM code. Significant increases in some organ doses (in mSv per injected activity) were found for (131)I and (124)I. The most affected organs were the intestinal walls, thyroid, and urinary bladder wall. Uncertainty remained similar to (123)I for case A but considerably greater for case B, especially for long biological half-lives (GI tract). Normal tissue dosimetries for IAZA must be considered carefully when substituting isotope species. A long biological half-life can significantly increase dosimetric uncertainties. These findings are relevant when considering PET imaging studies with [(124)I]IAZA or therapeutic administration of [(131)I]IAZA. MDPI 2022-08-09 /pmc/articles/PMC9416730/ /pubmed/36015281 http://dx.doi.org/10.3390/pharmaceutics14081655 Text en © 2022 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 Communication
Jans, Hans-S.
Stypinski, Daria
Kumar, Piyush
Mercer, John R.
McQuarrie, Stephen A.
McEwan, Alexander J. B.
Wiebe, Leonard I.
Radiation Dosimetry of Theragnostic Pairs for Isotopes of Iodine in IAZA
title Radiation Dosimetry of Theragnostic Pairs for Isotopes of Iodine in IAZA
title_full Radiation Dosimetry of Theragnostic Pairs for Isotopes of Iodine in IAZA
title_fullStr Radiation Dosimetry of Theragnostic Pairs for Isotopes of Iodine in IAZA
title_full_unstemmed Radiation Dosimetry of Theragnostic Pairs for Isotopes of Iodine in IAZA
title_short Radiation Dosimetry of Theragnostic Pairs for Isotopes of Iodine in IAZA
title_sort radiation dosimetry of theragnostic pairs for isotopes of iodine in iaza
topic Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9416730/
https://www.ncbi.nlm.nih.gov/pubmed/36015281
http://dx.doi.org/10.3390/pharmaceutics14081655
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