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Pulmonary toxicity of craniospinal irradiation using helical tomotherapy

Craniospinal irradiation using helical tomotherapy (HT-CSI) has advantages in aspects of homogeneous dose distribution. Physicians, however, still have concerns of pulmonary toxicity due to HT-CSI’s relatively large, low-dose irradiated volume from continuous and 360° rotation delivery. In this stud...

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Autores principales: Lee, Joongyo, Kim, Euidam, Kim, Nalee, Suh, Chang-Ok, Chung, Yoonsun, Yoon, Hong In
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8881492/
https://www.ncbi.nlm.nih.gov/pubmed/35217707
http://dx.doi.org/10.1038/s41598-022-07224-1
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author Lee, Joongyo
Kim, Euidam
Kim, Nalee
Suh, Chang-Ok
Chung, Yoonsun
Yoon, Hong In
author_facet Lee, Joongyo
Kim, Euidam
Kim, Nalee
Suh, Chang-Ok
Chung, Yoonsun
Yoon, Hong In
author_sort Lee, Joongyo
collection PubMed
description Craniospinal irradiation using helical tomotherapy (HT-CSI) has advantages in aspects of homogeneous dose distribution. Physicians, however, still have concerns of pulmonary toxicity due to HT-CSI’s relatively large, low-dose irradiated volume from continuous and 360° rotation delivery. In this study, we investigated the pulmonary toxicity of HT-CSI. We retrospectively reviewed 105 patients who received HT-CSI between January 2014 and December 2019. Grade 2 + pulmonary toxicities were evaluated. Intensive systemic treatment was defined as systemic treatment administration before, during, and after HT-CSI. V(X Gy) was defined as % volume receiving ≥ X Gy. Thirteen patients (12.4%) presented with grade 2 + pulmonary toxicities after HT-CSI. Of these patients, only one experienced grade 2 radiation pneumonitis combined with pembrolizumab-induced pneumonitis. Conversely, pneumonia was observed in 12 patients. Intensive systemic treatment (p = 0.004), immunosuppressive drugs (p = 0.031), and bilateral lung V(5 Gy) ≥ 65% (p = 0.031) were identified as independent risk factors for pneumonia. The risk factor for pneumonia in pediatric patients were immunosuppressive drugs (p = 0.035) and bilateral lung V(5 Gy) ≥ 65% (p = 0.047). HT-CSI can be a safe treatment modality with tolerable pulmonary toxicities. Intensive systemic treatment, immunosuppressive drugs, and bilateral lung V(5 Gy) ≥ 65% were significantly associated with pneumonia. In these patients, close follow-up should be considered for proper management of pneumonia.
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spelling pubmed-88814922022-03-01 Pulmonary toxicity of craniospinal irradiation using helical tomotherapy Lee, Joongyo Kim, Euidam Kim, Nalee Suh, Chang-Ok Chung, Yoonsun Yoon, Hong In Sci Rep Article Craniospinal irradiation using helical tomotherapy (HT-CSI) has advantages in aspects of homogeneous dose distribution. Physicians, however, still have concerns of pulmonary toxicity due to HT-CSI’s relatively large, low-dose irradiated volume from continuous and 360° rotation delivery. In this study, we investigated the pulmonary toxicity of HT-CSI. We retrospectively reviewed 105 patients who received HT-CSI between January 2014 and December 2019. Grade 2 + pulmonary toxicities were evaluated. Intensive systemic treatment was defined as systemic treatment administration before, during, and after HT-CSI. V(X Gy) was defined as % volume receiving ≥ X Gy. Thirteen patients (12.4%) presented with grade 2 + pulmonary toxicities after HT-CSI. Of these patients, only one experienced grade 2 radiation pneumonitis combined with pembrolizumab-induced pneumonitis. Conversely, pneumonia was observed in 12 patients. Intensive systemic treatment (p = 0.004), immunosuppressive drugs (p = 0.031), and bilateral lung V(5 Gy) ≥ 65% (p = 0.031) were identified as independent risk factors for pneumonia. The risk factor for pneumonia in pediatric patients were immunosuppressive drugs (p = 0.035) and bilateral lung V(5 Gy) ≥ 65% (p = 0.047). HT-CSI can be a safe treatment modality with tolerable pulmonary toxicities. Intensive systemic treatment, immunosuppressive drugs, and bilateral lung V(5 Gy) ≥ 65% were significantly associated with pneumonia. In these patients, close follow-up should be considered for proper management of pneumonia. Nature Publishing Group UK 2022-02-25 /pmc/articles/PMC8881492/ /pubmed/35217707 http://dx.doi.org/10.1038/s41598-022-07224-1 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This 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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Lee, Joongyo
Kim, Euidam
Kim, Nalee
Suh, Chang-Ok
Chung, Yoonsun
Yoon, Hong In
Pulmonary toxicity of craniospinal irradiation using helical tomotherapy
title Pulmonary toxicity of craniospinal irradiation using helical tomotherapy
title_full Pulmonary toxicity of craniospinal irradiation using helical tomotherapy
title_fullStr Pulmonary toxicity of craniospinal irradiation using helical tomotherapy
title_full_unstemmed Pulmonary toxicity of craniospinal irradiation using helical tomotherapy
title_short Pulmonary toxicity of craniospinal irradiation using helical tomotherapy
title_sort pulmonary toxicity of craniospinal irradiation using helical tomotherapy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8881492/
https://www.ncbi.nlm.nih.gov/pubmed/35217707
http://dx.doi.org/10.1038/s41598-022-07224-1
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