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Comparable Long-Term Tumor Control for Hypofractionated FLASH Versus Conventional Radiation Therapy in an Immunocompetent Rat Glioma Model

PURPOSE: To ensure a clinical translation of FLASH radiation therapy (FLASH-RT) for a specific tumor type, studies on tumor control and toxicity within the same biological system are needed. In this study, our objective was to evaluate tumor control and toxicity for hypofractionated FLASH-RT and con...

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Autores principales: Konradsson, Elise, Liljedahl, Emma, Gustafsson, Emma, Adrian, Gabriel, Beyer, Sarah, Ilaahi, Suhayb Ehsaan, Petersson, Kristoffer, Ceberg, Crister, Nittby Redebrandt, Henrietta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9449779/
https://www.ncbi.nlm.nih.gov/pubmed/36092986
http://dx.doi.org/10.1016/j.adro.2022.101011
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author Konradsson, Elise
Liljedahl, Emma
Gustafsson, Emma
Adrian, Gabriel
Beyer, Sarah
Ilaahi, Suhayb Ehsaan
Petersson, Kristoffer
Ceberg, Crister
Nittby Redebrandt, Henrietta
author_facet Konradsson, Elise
Liljedahl, Emma
Gustafsson, Emma
Adrian, Gabriel
Beyer, Sarah
Ilaahi, Suhayb Ehsaan
Petersson, Kristoffer
Ceberg, Crister
Nittby Redebrandt, Henrietta
author_sort Konradsson, Elise
collection PubMed
description PURPOSE: To ensure a clinical translation of FLASH radiation therapy (FLASH-RT) for a specific tumor type, studies on tumor control and toxicity within the same biological system are needed. In this study, our objective was to evaluate tumor control and toxicity for hypofractionated FLASH-RT and conventional radiation therapy (CONV-RT) in an immunocompetent rat glioma model. METHODS AND MATERIALS: Fisher 344 rats (N = 68) were inoculated subcutaneously with NS1 glioma cells and randomized into groups (n = 9-10 per group). CONV-RT (∼8 Gy/min) or FLASH-RT (70-90 Gy/s) was administered in 3 fractions of either 8 Gy, 12.5 Gy, or 15 Gy using a 10-MeV electron beam. The maximum tumor diameter was measured weekly, and overall survival was determined until day 100. Long-term tumor control was defined as no evident tumor on day 100. Animals were evaluated for acute dermal side effects at 2 to 5 weeks after completed RT and for late dermal side effects at 3 months after initiation of treatment. RESULTS: Survival was significantly increased in all irradiated groups compared with control animals (P < .001). In general, irradiated tumors started to shrink at 1 week post–completed RT. In 40% (23 of 58) of the irradiated animals, long-term tumor control was achieved. Radiation-induced skin toxic effects were mild and consisted of hair loss, erythema, and dry desquamation. No severe toxic effect was observed. There was no significant difference between FLASH-RT and CONV-RT in overall survival, acute side effects, or late side effects for any of the dose levels. CONCLUSIONS: This study shows that hypofractionated FLASH-RT results in long-term tumor control rates similar to those of CONV-RT for the treatment of large subcutaneous glioblastomas in immunocompetent rats. Neither treatment technique induced severe skin toxic effects. Consequently, no significant difference in toxicity could be resolved, suggesting that higher doses may be required to detect a FLASH sparing of skin.
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spelling pubmed-94497792022-09-08 Comparable Long-Term Tumor Control for Hypofractionated FLASH Versus Conventional Radiation Therapy in an Immunocompetent Rat Glioma Model Konradsson, Elise Liljedahl, Emma Gustafsson, Emma Adrian, Gabriel Beyer, Sarah Ilaahi, Suhayb Ehsaan Petersson, Kristoffer Ceberg, Crister Nittby Redebrandt, Henrietta Adv Radiat Oncol Scientific Article PURPOSE: To ensure a clinical translation of FLASH radiation therapy (FLASH-RT) for a specific tumor type, studies on tumor control and toxicity within the same biological system are needed. In this study, our objective was to evaluate tumor control and toxicity for hypofractionated FLASH-RT and conventional radiation therapy (CONV-RT) in an immunocompetent rat glioma model. METHODS AND MATERIALS: Fisher 344 rats (N = 68) were inoculated subcutaneously with NS1 glioma cells and randomized into groups (n = 9-10 per group). CONV-RT (∼8 Gy/min) or FLASH-RT (70-90 Gy/s) was administered in 3 fractions of either 8 Gy, 12.5 Gy, or 15 Gy using a 10-MeV electron beam. The maximum tumor diameter was measured weekly, and overall survival was determined until day 100. Long-term tumor control was defined as no evident tumor on day 100. Animals were evaluated for acute dermal side effects at 2 to 5 weeks after completed RT and for late dermal side effects at 3 months after initiation of treatment. RESULTS: Survival was significantly increased in all irradiated groups compared with control animals (P < .001). In general, irradiated tumors started to shrink at 1 week post–completed RT. In 40% (23 of 58) of the irradiated animals, long-term tumor control was achieved. Radiation-induced skin toxic effects were mild and consisted of hair loss, erythema, and dry desquamation. No severe toxic effect was observed. There was no significant difference between FLASH-RT and CONV-RT in overall survival, acute side effects, or late side effects for any of the dose levels. CONCLUSIONS: This study shows that hypofractionated FLASH-RT results in long-term tumor control rates similar to those of CONV-RT for the treatment of large subcutaneous glioblastomas in immunocompetent rats. Neither treatment technique induced severe skin toxic effects. Consequently, no significant difference in toxicity could be resolved, suggesting that higher doses may be required to detect a FLASH sparing of skin. Elsevier 2022-07-02 /pmc/articles/PMC9449779/ /pubmed/36092986 http://dx.doi.org/10.1016/j.adro.2022.101011 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Scientific Article
Konradsson, Elise
Liljedahl, Emma
Gustafsson, Emma
Adrian, Gabriel
Beyer, Sarah
Ilaahi, Suhayb Ehsaan
Petersson, Kristoffer
Ceberg, Crister
Nittby Redebrandt, Henrietta
Comparable Long-Term Tumor Control for Hypofractionated FLASH Versus Conventional Radiation Therapy in an Immunocompetent Rat Glioma Model
title Comparable Long-Term Tumor Control for Hypofractionated FLASH Versus Conventional Radiation Therapy in an Immunocompetent Rat Glioma Model
title_full Comparable Long-Term Tumor Control for Hypofractionated FLASH Versus Conventional Radiation Therapy in an Immunocompetent Rat Glioma Model
title_fullStr Comparable Long-Term Tumor Control for Hypofractionated FLASH Versus Conventional Radiation Therapy in an Immunocompetent Rat Glioma Model
title_full_unstemmed Comparable Long-Term Tumor Control for Hypofractionated FLASH Versus Conventional Radiation Therapy in an Immunocompetent Rat Glioma Model
title_short Comparable Long-Term Tumor Control for Hypofractionated FLASH Versus Conventional Radiation Therapy in an Immunocompetent Rat Glioma Model
title_sort comparable long-term tumor control for hypofractionated flash versus conventional radiation therapy in an immunocompetent rat glioma model
topic Scientific Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9449779/
https://www.ncbi.nlm.nih.gov/pubmed/36092986
http://dx.doi.org/10.1016/j.adro.2022.101011
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