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Evaluation of the systematic error in using 3D dose calculation in scanning beam proton therapy for lung cancer

The objective of this study was to evaluate and understand the systematic error between the planned three‐dimensional (3D) dose and the delivered dose to patient in scanning beam proton therapy for lung tumors. Single‐field and multifield optimized scanning beam proton therapy plans were generated f...

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Autores principales: Li, Heng, Liu, Wei, Park, Peter, Matney, Jason, Liao, Zhongxing, Chang, Joe, Zhang, Xiaodong, Li, Yupeng, Zhu, Ronald X
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4161985/
https://www.ncbi.nlm.nih.gov/pubmed/25207565
http://dx.doi.org/10.1120/jacmp.v15i5.4810
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author Li, Heng
Liu, Wei
Park, Peter
Matney, Jason
Liao, Zhongxing
Chang, Joe
Zhang, Xiaodong
Li, Yupeng
Zhu, Ronald X
author_facet Li, Heng
Liu, Wei
Park, Peter
Matney, Jason
Liao, Zhongxing
Chang, Joe
Zhang, Xiaodong
Li, Yupeng
Zhu, Ronald X
author_sort Li, Heng
collection PubMed
description The objective of this study was to evaluate and understand the systematic error between the planned three‐dimensional (3D) dose and the delivered dose to patient in scanning beam proton therapy for lung tumors. Single‐field and multifield optimized scanning beam proton therapy plans were generated for ten patients with stage II‐III lung cancer with a mix of tumor motion and size. 3D doses in CT datasets for different respiratory phases and the time‐weighted average CT, as well as the four‐dimensional (4D) doses were computed for both plans. The 3D and 4D dose differences for the targets and different organs at risk were compared using dose‐volume histogram (DVH) and voxel‐based techniques, and correlated with the extent of tumor motion. The gross tumor volume (GTV) dose was maintained in all 3D and 4D doses, using the internal GTV override technique. The DVH and voxel‐based techniques are highly correlated. The mean dose error and the standard deviation of dose error for all target volumes were both less than 1.5% for all but one patient. However, the point dose difference between the 3D and 4D doses was up to 6% for the GTV and greater than 10% for the clinical and planning target volumes. Changes in the 4D and 3D doses were not correlated with tumor motion. The planning technique (single‐field or multifield optimized) did not affect the observed systematic error. In conclusion, the dose error in 3D dose calculation varies from patient to patient and does not correlate with lung tumor motion. Therefore, patient‐specific evaluation of the 4D dose is important for scanning beam proton therapy for lung tumors. PACS number: 87.55.D
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spelling pubmed-41619852018-04-02 Evaluation of the systematic error in using 3D dose calculation in scanning beam proton therapy for lung cancer Li, Heng Liu, Wei Park, Peter Matney, Jason Liao, Zhongxing Chang, Joe Zhang, Xiaodong Li, Yupeng Zhu, Ronald X J Appl Clin Med Phys Radiation Oncology Physics The objective of this study was to evaluate and understand the systematic error between the planned three‐dimensional (3D) dose and the delivered dose to patient in scanning beam proton therapy for lung tumors. Single‐field and multifield optimized scanning beam proton therapy plans were generated for ten patients with stage II‐III lung cancer with a mix of tumor motion and size. 3D doses in CT datasets for different respiratory phases and the time‐weighted average CT, as well as the four‐dimensional (4D) doses were computed for both plans. The 3D and 4D dose differences for the targets and different organs at risk were compared using dose‐volume histogram (DVH) and voxel‐based techniques, and correlated with the extent of tumor motion. The gross tumor volume (GTV) dose was maintained in all 3D and 4D doses, using the internal GTV override technique. The DVH and voxel‐based techniques are highly correlated. The mean dose error and the standard deviation of dose error for all target volumes were both less than 1.5% for all but one patient. However, the point dose difference between the 3D and 4D doses was up to 6% for the GTV and greater than 10% for the clinical and planning target volumes. Changes in the 4D and 3D doses were not correlated with tumor motion. The planning technique (single‐field or multifield optimized) did not affect the observed systematic error. In conclusion, the dose error in 3D dose calculation varies from patient to patient and does not correlate with lung tumor motion. Therefore, patient‐specific evaluation of the 4D dose is important for scanning beam proton therapy for lung tumors. PACS number: 87.55.D John Wiley and Sons Inc. 2014-09-08 /pmc/articles/PMC4161985/ /pubmed/25207565 http://dx.doi.org/10.1120/jacmp.v15i5.4810 Text en © 2014 The Authors. This is an open access article under the terms of the 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
Li, Heng
Liu, Wei
Park, Peter
Matney, Jason
Liao, Zhongxing
Chang, Joe
Zhang, Xiaodong
Li, Yupeng
Zhu, Ronald X
Evaluation of the systematic error in using 3D dose calculation in scanning beam proton therapy for lung cancer
title Evaluation of the systematic error in using 3D dose calculation in scanning beam proton therapy for lung cancer
title_full Evaluation of the systematic error in using 3D dose calculation in scanning beam proton therapy for lung cancer
title_fullStr Evaluation of the systematic error in using 3D dose calculation in scanning beam proton therapy for lung cancer
title_full_unstemmed Evaluation of the systematic error in using 3D dose calculation in scanning beam proton therapy for lung cancer
title_short Evaluation of the systematic error in using 3D dose calculation in scanning beam proton therapy for lung cancer
title_sort evaluation of the systematic error in using 3d dose calculation in scanning beam proton therapy for lung cancer
topic Radiation Oncology Physics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4161985/
https://www.ncbi.nlm.nih.gov/pubmed/25207565
http://dx.doi.org/10.1120/jacmp.v15i5.4810
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