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Feasibility of a mini-pig model of radiation-induced brain injury to one cerebral hemisphere

BACKGROUND: Radiation-induced brain injury is a common concern for survivors of adult and pediatric brain cancer. Pre-clinically, rodent models are the standard approach to evaluate mechanisms of injury and test new therapeutics for this condition. However, these rodent models fail to recapitulate t...

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Autores principales: Athanasiadi, Ilektra, Perez, Whitney D., Plantenga, Jeannie M., Jones-Hall, Yava, Perez-Torres, Carlos J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7866466/
https://www.ncbi.nlm.nih.gov/pubmed/33549130
http://dx.doi.org/10.1186/s13014-021-01753-1
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author Athanasiadi, Ilektra
Perez, Whitney D.
Plantenga, Jeannie M.
Jones-Hall, Yava
Perez-Torres, Carlos J.
author_facet Athanasiadi, Ilektra
Perez, Whitney D.
Plantenga, Jeannie M.
Jones-Hall, Yava
Perez-Torres, Carlos J.
author_sort Athanasiadi, Ilektra
collection PubMed
description BACKGROUND: Radiation-induced brain injury is a common concern for survivors of adult and pediatric brain cancer. Pre-clinically, rodent models are the standard approach to evaluate mechanisms of injury and test new therapeutics for this condition. However, these rodent models fail to recapitulate the radiological and histological characteristics of the clinical disease. METHODS: Here we describe a hemispheric mini-pig model of radiation-induced brain injury generated with a clinical 6 MV photon irradiator and evaluated with a clinical 3T MRI. Two pairs of Yucatan mini-pigs each received either 15 Gy or 25 Gy to the left brain hemisphere. Quality of intensity modulated radiation therapy treatment plans was evaluated retrospectively with parameters reported according to ICRU guidelines. The pigs were observed weekly to check for any outright signs of neurological impairment. The pigs underwent anatomical MRI examination before irradiation and up to 6 months post-irradiation. Immediately after the last imaging time point, the pigs were euthanized and their brains were collected for histopathological assessment. RESULTS: Analysis of the dose volume histograms showed that 93% of the prescribed dose was delivered to at least 93% of the target volume in the left hemisphere. Organs at risk excluded from the target volume received doses below clinical safety thresholds. For the pigs that received a 25 Gy dose, progressive neurological impairment was observed starting at 2 months post-irradiation leading to the need for euthanasia by 3–4 months. On MRI, these two animals presented with diffuse white matter pathology consistent with the human disease that progressed to outright radiation necrosis and severe brain swelling. Histology was consistent with the final MRI evaluation. The pigs that received a 15 Gy dose appeared normal all the way to 6 months post-irradiation with no obvious neurological impairment or lesions on MRI or histopathology. CONCLUSION: Based on our results, a mini-pig model of radiation-induced brain injury is feasible though some optimization is still needed. The mini-pig model produced lesions on MRI that are consistent with the human disease and which are not seen in rodent models. Our data shows that the ideal radiation dose for this model likely lies between 15 and 25 Gy.
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spelling pubmed-78664662021-02-08 Feasibility of a mini-pig model of radiation-induced brain injury to one cerebral hemisphere Athanasiadi, Ilektra Perez, Whitney D. Plantenga, Jeannie M. Jones-Hall, Yava Perez-Torres, Carlos J. Radiat Oncol Methodology BACKGROUND: Radiation-induced brain injury is a common concern for survivors of adult and pediatric brain cancer. Pre-clinically, rodent models are the standard approach to evaluate mechanisms of injury and test new therapeutics for this condition. However, these rodent models fail to recapitulate the radiological and histological characteristics of the clinical disease. METHODS: Here we describe a hemispheric mini-pig model of radiation-induced brain injury generated with a clinical 6 MV photon irradiator and evaluated with a clinical 3T MRI. Two pairs of Yucatan mini-pigs each received either 15 Gy or 25 Gy to the left brain hemisphere. Quality of intensity modulated radiation therapy treatment plans was evaluated retrospectively with parameters reported according to ICRU guidelines. The pigs were observed weekly to check for any outright signs of neurological impairment. The pigs underwent anatomical MRI examination before irradiation and up to 6 months post-irradiation. Immediately after the last imaging time point, the pigs were euthanized and their brains were collected for histopathological assessment. RESULTS: Analysis of the dose volume histograms showed that 93% of the prescribed dose was delivered to at least 93% of the target volume in the left hemisphere. Organs at risk excluded from the target volume received doses below clinical safety thresholds. For the pigs that received a 25 Gy dose, progressive neurological impairment was observed starting at 2 months post-irradiation leading to the need for euthanasia by 3–4 months. On MRI, these two animals presented with diffuse white matter pathology consistent with the human disease that progressed to outright radiation necrosis and severe brain swelling. Histology was consistent with the final MRI evaluation. The pigs that received a 15 Gy dose appeared normal all the way to 6 months post-irradiation with no obvious neurological impairment or lesions on MRI or histopathology. CONCLUSION: Based on our results, a mini-pig model of radiation-induced brain injury is feasible though some optimization is still needed. The mini-pig model produced lesions on MRI that are consistent with the human disease and which are not seen in rodent models. Our data shows that the ideal radiation dose for this model likely lies between 15 and 25 Gy. BioMed Central 2021-02-06 /pmc/articles/PMC7866466/ /pubmed/33549130 http://dx.doi.org/10.1186/s13014-021-01753-1 Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Methodology
Athanasiadi, Ilektra
Perez, Whitney D.
Plantenga, Jeannie M.
Jones-Hall, Yava
Perez-Torres, Carlos J.
Feasibility of a mini-pig model of radiation-induced brain injury to one cerebral hemisphere
title Feasibility of a mini-pig model of radiation-induced brain injury to one cerebral hemisphere
title_full Feasibility of a mini-pig model of radiation-induced brain injury to one cerebral hemisphere
title_fullStr Feasibility of a mini-pig model of radiation-induced brain injury to one cerebral hemisphere
title_full_unstemmed Feasibility of a mini-pig model of radiation-induced brain injury to one cerebral hemisphere
title_short Feasibility of a mini-pig model of radiation-induced brain injury to one cerebral hemisphere
title_sort feasibility of a mini-pig model of radiation-induced brain injury to one cerebral hemisphere
topic Methodology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7866466/
https://www.ncbi.nlm.nih.gov/pubmed/33549130
http://dx.doi.org/10.1186/s13014-021-01753-1
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