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Reducing the number of CTs performed to monitor personalized dosimetry during peptide receptor radionuclide therapy (PRRT)

BACKGROUND: Peptide receptor radionuclide therapy (PRRT) with [(177)Lu]-DOTA-TATE is an effective treatment of neuroendocrine tumors (NETs). After each cycle of treatment, patient dosimetry evaluates the radiation dose to the risk organs, kidneys, and bone marrow, the most radiosensitive tissues. Ab...

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Autores principales: Chicheportiche, Alexandre, Artoul, Faozi, Schwartz, Arnon, Grozinsky-Glasberg, Simona, Meirovitz, Amichay, Gross, David J., Godefroy, Jeremy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6006002/
https://www.ncbi.nlm.nih.gov/pubmed/29916115
http://dx.doi.org/10.1186/s40658-018-0211-1
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author Chicheportiche, Alexandre
Artoul, Faozi
Schwartz, Arnon
Grozinsky-Glasberg, Simona
Meirovitz, Amichay
Gross, David J.
Godefroy, Jeremy
author_facet Chicheportiche, Alexandre
Artoul, Faozi
Schwartz, Arnon
Grozinsky-Glasberg, Simona
Meirovitz, Amichay
Gross, David J.
Godefroy, Jeremy
author_sort Chicheportiche, Alexandre
collection PubMed
description BACKGROUND: Peptide receptor radionuclide therapy (PRRT) with [(177)Lu]-DOTA-TATE is an effective treatment of neuroendocrine tumors (NETs). After each cycle of treatment, patient dosimetry evaluates the radiation dose to the risk organs, kidneys, and bone marrow, the most radiosensitive tissues. Absorbed doses are calculated from the radioactivity in the blood and from single photon emission computed tomography (SPECT) images corrected by computed tomography (CT) acquired after each course of treatment. The aim of this work is to assess whether the dosimetry along all treatment cycles can be calculated using a single CT. We hypothesize that the absorbed doses to the risk organs calculated with a single CT will be accurate enough to correctly manage the patients, i.e., whether or not to continue PRRT. Twenty-four patients diagnosed with metastatic NETs undergoing PRRT with [(177)Lu]-DOTA-TATE were retrospectively included in this study. We compared radiation doses to the kidneys and bone marrow using two protocols. In the “classical” one, dosimetry is calculated based on a SPECT and a CT after each treatment cycle. In the new protocol, dosimetry is calculated based on a SPECT study after each cycle but with the first acquired CT for all cycles. RESULTS: The decision whether or not to stop PRRT because of unsafe absorbed dose to the risk organs would have been the same had the classical or the new protocol been used. The agreement between the cumulative doses to the kidneys and bone marrow obtained from the two protocols was excellent with Pearson’s correlation coefficients r = 0.95 and r = 0.99 (P < 0.0001) and mean relative differences of 5.30 ± 6.20% and 0.48 ± 4.88%, respectively. CONCLUSIONS: Dosimetry calculations for a given patient can be done using a single CT registered to serial SPECTs. This new protocol reduces the need for a hybrid camera in the follow-up of patients receiving [(177)Lu]-DOTA-TATE.
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spelling pubmed-60060022018-07-03 Reducing the number of CTs performed to monitor personalized dosimetry during peptide receptor radionuclide therapy (PRRT) Chicheportiche, Alexandre Artoul, Faozi Schwartz, Arnon Grozinsky-Glasberg, Simona Meirovitz, Amichay Gross, David J. Godefroy, Jeremy EJNMMI Phys Original Research BACKGROUND: Peptide receptor radionuclide therapy (PRRT) with [(177)Lu]-DOTA-TATE is an effective treatment of neuroendocrine tumors (NETs). After each cycle of treatment, patient dosimetry evaluates the radiation dose to the risk organs, kidneys, and bone marrow, the most radiosensitive tissues. Absorbed doses are calculated from the radioactivity in the blood and from single photon emission computed tomography (SPECT) images corrected by computed tomography (CT) acquired after each course of treatment. The aim of this work is to assess whether the dosimetry along all treatment cycles can be calculated using a single CT. We hypothesize that the absorbed doses to the risk organs calculated with a single CT will be accurate enough to correctly manage the patients, i.e., whether or not to continue PRRT. Twenty-four patients diagnosed with metastatic NETs undergoing PRRT with [(177)Lu]-DOTA-TATE were retrospectively included in this study. We compared radiation doses to the kidneys and bone marrow using two protocols. In the “classical” one, dosimetry is calculated based on a SPECT and a CT after each treatment cycle. In the new protocol, dosimetry is calculated based on a SPECT study after each cycle but with the first acquired CT for all cycles. RESULTS: The decision whether or not to stop PRRT because of unsafe absorbed dose to the risk organs would have been the same had the classical or the new protocol been used. The agreement between the cumulative doses to the kidneys and bone marrow obtained from the two protocols was excellent with Pearson’s correlation coefficients r = 0.95 and r = 0.99 (P < 0.0001) and mean relative differences of 5.30 ± 6.20% and 0.48 ± 4.88%, respectively. CONCLUSIONS: Dosimetry calculations for a given patient can be done using a single CT registered to serial SPECTs. This new protocol reduces the need for a hybrid camera in the follow-up of patients receiving [(177)Lu]-DOTA-TATE. Springer International Publishing 2018-06-19 /pmc/articles/PMC6006002/ /pubmed/29916115 http://dx.doi.org/10.1186/s40658-018-0211-1 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Research
Chicheportiche, Alexandre
Artoul, Faozi
Schwartz, Arnon
Grozinsky-Glasberg, Simona
Meirovitz, Amichay
Gross, David J.
Godefroy, Jeremy
Reducing the number of CTs performed to monitor personalized dosimetry during peptide receptor radionuclide therapy (PRRT)
title Reducing the number of CTs performed to monitor personalized dosimetry during peptide receptor radionuclide therapy (PRRT)
title_full Reducing the number of CTs performed to monitor personalized dosimetry during peptide receptor radionuclide therapy (PRRT)
title_fullStr Reducing the number of CTs performed to monitor personalized dosimetry during peptide receptor radionuclide therapy (PRRT)
title_full_unstemmed Reducing the number of CTs performed to monitor personalized dosimetry during peptide receptor radionuclide therapy (PRRT)
title_short Reducing the number of CTs performed to monitor personalized dosimetry during peptide receptor radionuclide therapy (PRRT)
title_sort reducing the number of cts performed to monitor personalized dosimetry during peptide receptor radionuclide therapy (prrt)
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6006002/
https://www.ncbi.nlm.nih.gov/pubmed/29916115
http://dx.doi.org/10.1186/s40658-018-0211-1
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