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The new SRS/FSRT technique HyperArc for benign brain lesions: a dosimetric analysis

To evaluate the potential benefit of HyperArc (HA) fractionated stereotactic radiotherapy (FSRT) for the benign brain lesion. Sixteen patients with a single deep-seated, centrally located benign brain lesion treated by CyberKnife (CK, G4 cone-based model) were enrolled. Treatment plans for HA with t...

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Autores principales: Ho, Hsiu-Wen, Yang, Ching-Chieh, Lin, Hsiu-Man, Chen, Hsiao-Yun, Huang, Chun-Chiao, Wang, Shih-Chang, Lin, Yu-Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8548509/
https://www.ncbi.nlm.nih.gov/pubmed/34702859
http://dx.doi.org/10.1038/s41598-021-00381-9
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author Ho, Hsiu-Wen
Yang, Ching-Chieh
Lin, Hsiu-Man
Chen, Hsiao-Yun
Huang, Chun-Chiao
Wang, Shih-Chang
Lin, Yu-Wei
author_facet Ho, Hsiu-Wen
Yang, Ching-Chieh
Lin, Hsiu-Man
Chen, Hsiao-Yun
Huang, Chun-Chiao
Wang, Shih-Chang
Lin, Yu-Wei
author_sort Ho, Hsiu-Wen
collection PubMed
description To evaluate the potential benefit of HyperArc (HA) fractionated stereotactic radiotherapy (FSRT) for the benign brain lesion. Sixteen patients with a single deep-seated, centrally located benign brain lesion treated by CyberKnife (CK, G4 cone-based model) were enrolled. Treatment plans for HA with two different optimization algorithms (SRS NTO and ALDO) and coplanar RapidArc (RA) were generated for each patient to meet the corresponding treatment plan criteria. These four FSRT treatment plans were divided into two groups—the homogeneous delivery group (HA-SRS NTO and coplanar RA) and the inhomogeneous delivery group (HA-ALDO and cone-based CK)—to compare for dosimetric outcomes. For homogeneous delivery, the brain V5, V12, and V24 and the mean brainstem dose were significantly lower with the HA-SRS NTO plans than with the coplanar RA plans. The conformity index, high and intermediate dose spillage, and gradient radius were significantly better with the HA-SRS NTO plans than with the coplanar RA plans. For inhomogeneous delivery, the HA-ALDO exhibited superior PTV coverage levels to the cone-based CK plans. Almost all the doses delivered to organs at risk and dose distribution metrics were significantly better with the HA-ALDO plans than with the cone-based CK plans. Good dosimetric distribution makes HA an attractive FSRT technique for the treatment of benign brain lesions.
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spelling pubmed-85485092021-10-28 The new SRS/FSRT technique HyperArc for benign brain lesions: a dosimetric analysis Ho, Hsiu-Wen Yang, Ching-Chieh Lin, Hsiu-Man Chen, Hsiao-Yun Huang, Chun-Chiao Wang, Shih-Chang Lin, Yu-Wei Sci Rep Article To evaluate the potential benefit of HyperArc (HA) fractionated stereotactic radiotherapy (FSRT) for the benign brain lesion. Sixteen patients with a single deep-seated, centrally located benign brain lesion treated by CyberKnife (CK, G4 cone-based model) were enrolled. Treatment plans for HA with two different optimization algorithms (SRS NTO and ALDO) and coplanar RapidArc (RA) were generated for each patient to meet the corresponding treatment plan criteria. These four FSRT treatment plans were divided into two groups—the homogeneous delivery group (HA-SRS NTO and coplanar RA) and the inhomogeneous delivery group (HA-ALDO and cone-based CK)—to compare for dosimetric outcomes. For homogeneous delivery, the brain V5, V12, and V24 and the mean brainstem dose were significantly lower with the HA-SRS NTO plans than with the coplanar RA plans. The conformity index, high and intermediate dose spillage, and gradient radius were significantly better with the HA-SRS NTO plans than with the coplanar RA plans. For inhomogeneous delivery, the HA-ALDO exhibited superior PTV coverage levels to the cone-based CK plans. Almost all the doses delivered to organs at risk and dose distribution metrics were significantly better with the HA-ALDO plans than with the cone-based CK plans. Good dosimetric distribution makes HA an attractive FSRT technique for the treatment of benign brain lesions. Nature Publishing Group UK 2021-10-26 /pmc/articles/PMC8548509/ /pubmed/34702859 http://dx.doi.org/10.1038/s41598-021-00381-9 Text en © The Author(s) 2021 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
Ho, Hsiu-Wen
Yang, Ching-Chieh
Lin, Hsiu-Man
Chen, Hsiao-Yun
Huang, Chun-Chiao
Wang, Shih-Chang
Lin, Yu-Wei
The new SRS/FSRT technique HyperArc for benign brain lesions: a dosimetric analysis
title The new SRS/FSRT technique HyperArc for benign brain lesions: a dosimetric analysis
title_full The new SRS/FSRT technique HyperArc for benign brain lesions: a dosimetric analysis
title_fullStr The new SRS/FSRT technique HyperArc for benign brain lesions: a dosimetric analysis
title_full_unstemmed The new SRS/FSRT technique HyperArc for benign brain lesions: a dosimetric analysis
title_short The new SRS/FSRT technique HyperArc for benign brain lesions: a dosimetric analysis
title_sort new srs/fsrt technique hyperarc for benign brain lesions: a dosimetric analysis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8548509/
https://www.ncbi.nlm.nih.gov/pubmed/34702859
http://dx.doi.org/10.1038/s41598-021-00381-9
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