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Beyond the heart in hypofractionated radiotherapy and in the transition from 3D to IMRT/VMAT

BACKGROUND: The knowledge of the risks induced by radiation with hypofractionation regimens has only recently been estimated together with its implementation as a management standard. However, the dose to other risk organs with intensity-modulated radiation therapy (IMRT) or volumetric modulated arc...

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Autores principales: Mondragon, Lorena Lio, Lopez, Hidralba Pérez, Diaz, Adolfo Fernández, Lio, Iván Avilés, Guzman, Alejandro Olmos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Via Medica 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10547416/
https://www.ncbi.nlm.nih.gov/pubmed/37795223
http://dx.doi.org/10.5603/RPOR.a2023.0053
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author Mondragon, Lorena Lio
Lopez, Hidralba Pérez
Diaz, Adolfo Fernández
Lio, Iván Avilés
Guzman, Alejandro Olmos
author_facet Mondragon, Lorena Lio
Lopez, Hidralba Pérez
Diaz, Adolfo Fernández
Lio, Iván Avilés
Guzman, Alejandro Olmos
author_sort Mondragon, Lorena Lio
collection PubMed
description BACKGROUND: The knowledge of the risks induced by radiation with hypofractionation regimens has only recently been estimated together with its implementation as a management standard. However, the dose to other risk organs with intensity-modulated radiation therapy (IMRT) or volumetric modulated arc therapy (VMAT) is not clear, that is why this is only a reference study of radiation doses to organs at risk in hypofractionation in our center. MATERIALS AND METHODS: We completed a retrospective and observational analysis of 1398 patients treated with adjuvant hypofractionated radiotherapy from 2015 to 2018, using the clinical records and dose-volume histogram of patients treated with moderate hypofractionated adjuvant radiotherapy. To analyze the institutional experience on the dosimetry of the esophagus and liver as risk organs in the use of moderate adjuvant hypofractionated radiotherapy in breast cancer. RESULTS: The dosimetry of the esophagus was 3271 cGy DMax, 177 cGy DMed, 68 cGy D50%, 500 cGy DcMAX with 3D RT and 4124 cGy DMax, 1242 cGy DMed, 934.50 cGy D50%, 3213 cGy DcMAX with IMRT/VMAT and the dosimetry for the liver was for right breast cancer 466 cGy DMed, 102 cGy D50% and 8% V20, for left breast cancer 22 cGy DMed, 6.10 cGy D50% and 0.3% V20. CONCLUSION: The statistically significant differences in irradiation show the lack of consensus on the optimal restrictions in hypofractionation regimens to reduce clinical sequela; consequently, the variability in the specification of each radiation oncologist is observed; standardization in our center can lead to improvement in the quality of treatments.
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spelling pubmed-105474162023-10-04 Beyond the heart in hypofractionated radiotherapy and in the transition from 3D to IMRT/VMAT Mondragon, Lorena Lio Lopez, Hidralba Pérez Diaz, Adolfo Fernández Lio, Iván Avilés Guzman, Alejandro Olmos Rep Pract Oncol Radiother Research Paper BACKGROUND: The knowledge of the risks induced by radiation with hypofractionation regimens has only recently been estimated together with its implementation as a management standard. However, the dose to other risk organs with intensity-modulated radiation therapy (IMRT) or volumetric modulated arc therapy (VMAT) is not clear, that is why this is only a reference study of radiation doses to organs at risk in hypofractionation in our center. MATERIALS AND METHODS: We completed a retrospective and observational analysis of 1398 patients treated with adjuvant hypofractionated radiotherapy from 2015 to 2018, using the clinical records and dose-volume histogram of patients treated with moderate hypofractionated adjuvant radiotherapy. To analyze the institutional experience on the dosimetry of the esophagus and liver as risk organs in the use of moderate adjuvant hypofractionated radiotherapy in breast cancer. RESULTS: The dosimetry of the esophagus was 3271 cGy DMax, 177 cGy DMed, 68 cGy D50%, 500 cGy DcMAX with 3D RT and 4124 cGy DMax, 1242 cGy DMed, 934.50 cGy D50%, 3213 cGy DcMAX with IMRT/VMAT and the dosimetry for the liver was for right breast cancer 466 cGy DMed, 102 cGy D50% and 8% V20, for left breast cancer 22 cGy DMed, 6.10 cGy D50% and 0.3% V20. CONCLUSION: The statistically significant differences in irradiation show the lack of consensus on the optimal restrictions in hypofractionation regimens to reduce clinical sequela; consequently, the variability in the specification of each radiation oncologist is observed; standardization in our center can lead to improvement in the quality of treatments. Via Medica 2023-08-28 /pmc/articles/PMC10547416/ /pubmed/37795223 http://dx.doi.org/10.5603/RPOR.a2023.0053 Text en © 2023 Greater Poland Cancer Centre https://creativecommons.org/licenses/by-nc-nd/4.0/This article is available in open access under Creative Common Attribution-Non-Commercial-No Derivatives 4.0 International (CC BY-NC-ND 4.0) license, allowing to download articles and share them with others as long as they credit the authors and the publisher, but without permission to change them in any way or use them commercially
spellingShingle Research Paper
Mondragon, Lorena Lio
Lopez, Hidralba Pérez
Diaz, Adolfo Fernández
Lio, Iván Avilés
Guzman, Alejandro Olmos
Beyond the heart in hypofractionated radiotherapy and in the transition from 3D to IMRT/VMAT
title Beyond the heart in hypofractionated radiotherapy and in the transition from 3D to IMRT/VMAT
title_full Beyond the heart in hypofractionated radiotherapy and in the transition from 3D to IMRT/VMAT
title_fullStr Beyond the heart in hypofractionated radiotherapy and in the transition from 3D to IMRT/VMAT
title_full_unstemmed Beyond the heart in hypofractionated radiotherapy and in the transition from 3D to IMRT/VMAT
title_short Beyond the heart in hypofractionated radiotherapy and in the transition from 3D to IMRT/VMAT
title_sort beyond the heart in hypofractionated radiotherapy and in the transition from 3d to imrt/vmat
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10547416/
https://www.ncbi.nlm.nih.gov/pubmed/37795223
http://dx.doi.org/10.5603/RPOR.a2023.0053
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