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Evaluation of tumor motion effects on dose distribution for hypofractionated intensity‐modulated radiotherapy of non‐small‐cell lung cancer
Respiration‐induced tumor motion during intensity‐modulated radiotherapy (IMRT) of non‐small‐cell lung cancer (NSCLC) could cause substantial differences between planned and delivered doses. While it has been shown that, for conventionally fractionated IMRT, motion effects average out over the cours...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2924766/ https://www.ncbi.nlm.nih.gov/pubmed/20717084 http://dx.doi.org/10.1120/jacmp.v11i3.3182 |
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author | Kang, Hyejoo Yorke, Ellen D. Yang, Jie Chui, Chen‐Shou Rosenzweig, Kenneth E. Amols, Howard I. |
author_facet | Kang, Hyejoo Yorke, Ellen D. Yang, Jie Chui, Chen‐Shou Rosenzweig, Kenneth E. Amols, Howard I. |
author_sort | Kang, Hyejoo |
collection | PubMed |
description | Respiration‐induced tumor motion during intensity‐modulated radiotherapy (IMRT) of non‐small‐cell lung cancer (NSCLC) could cause substantial differences between planned and delivered doses. While it has been shown that, for conventionally fractionated IMRT, motion effects average out over the course of many treatments, this might not be true for hypofractionated IMRT (IMHFRT). Numerical simulations were performed for nine NSCLC patients (11 tumors) to evaluate this problem. Dose distributions to the Clinical Target Volume (CTV) and Internal Target Volume (ITV) were retrospectively calculated using the previously‐calculated leaf motion files but with the addition of typical periodic motion (i.e. amplitude 0.36–1.26 cm, 3–8 sec period). A typical IMHFRT prescription of [Formula: see text] fractions was assumed. For the largest amplitude (1.26 cm), the average ± standard deviation of the ratio of simulated to planned mean dose, minimum dose, D95 and V95 were [Formula: see text] , [Formula: see text] , [Formula: see text] and [Formula: see text] for the CTV, and [Formula: see text] , [Formula: see text] , [Formula: see text] and [Formula: see text] for the ITV, respectively. There was minimal dependence on period or initial phase. For typical tumor geometries and respiratory amplitudes, changes in target coverage are minimal but can be significant for larger amplitudes, faster beam delivery, more highly‐modulated fields, and smaller field margins. PACS number: 87.55.dk |
format | Text |
id | pubmed-2924766 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-29247662018-04-02 Evaluation of tumor motion effects on dose distribution for hypofractionated intensity‐modulated radiotherapy of non‐small‐cell lung cancer Kang, Hyejoo Yorke, Ellen D. Yang, Jie Chui, Chen‐Shou Rosenzweig, Kenneth E. Amols, Howard I. J Appl Clin Med Phys Radiation Oncology Physics Respiration‐induced tumor motion during intensity‐modulated radiotherapy (IMRT) of non‐small‐cell lung cancer (NSCLC) could cause substantial differences between planned and delivered doses. While it has been shown that, for conventionally fractionated IMRT, motion effects average out over the course of many treatments, this might not be true for hypofractionated IMRT (IMHFRT). Numerical simulations were performed for nine NSCLC patients (11 tumors) to evaluate this problem. Dose distributions to the Clinical Target Volume (CTV) and Internal Target Volume (ITV) were retrospectively calculated using the previously‐calculated leaf motion files but with the addition of typical periodic motion (i.e. amplitude 0.36–1.26 cm, 3–8 sec period). A typical IMHFRT prescription of [Formula: see text] fractions was assumed. For the largest amplitude (1.26 cm), the average ± standard deviation of the ratio of simulated to planned mean dose, minimum dose, D95 and V95 were [Formula: see text] , [Formula: see text] , [Formula: see text] and [Formula: see text] for the CTV, and [Formula: see text] , [Formula: see text] , [Formula: see text] and [Formula: see text] for the ITV, respectively. There was minimal dependence on period or initial phase. For typical tumor geometries and respiratory amplitudes, changes in target coverage are minimal but can be significant for larger amplitudes, faster beam delivery, more highly‐modulated fields, and smaller field margins. PACS number: 87.55.dk John Wiley and Sons Inc. 2010-06-08 /pmc/articles/PMC2924766/ /pubmed/20717084 http://dx.doi.org/10.1120/jacmp.v11i3.3182 Text en © 2010 The Authors. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/3.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Radiation Oncology Physics Kang, Hyejoo Yorke, Ellen D. Yang, Jie Chui, Chen‐Shou Rosenzweig, Kenneth E. Amols, Howard I. Evaluation of tumor motion effects on dose distribution for hypofractionated intensity‐modulated radiotherapy of non‐small‐cell lung cancer |
title | Evaluation of tumor motion effects on dose distribution for hypofractionated intensity‐modulated radiotherapy of non‐small‐cell lung cancer |
title_full | Evaluation of tumor motion effects on dose distribution for hypofractionated intensity‐modulated radiotherapy of non‐small‐cell lung cancer |
title_fullStr | Evaluation of tumor motion effects on dose distribution for hypofractionated intensity‐modulated radiotherapy of non‐small‐cell lung cancer |
title_full_unstemmed | Evaluation of tumor motion effects on dose distribution for hypofractionated intensity‐modulated radiotherapy of non‐small‐cell lung cancer |
title_short | Evaluation of tumor motion effects on dose distribution for hypofractionated intensity‐modulated radiotherapy of non‐small‐cell lung cancer |
title_sort | evaluation of tumor motion effects on dose distribution for hypofractionated intensity‐modulated radiotherapy of non‐small‐cell lung cancer |
topic | Radiation Oncology Physics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2924766/ https://www.ncbi.nlm.nih.gov/pubmed/20717084 http://dx.doi.org/10.1120/jacmp.v11i3.3182 |
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