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Impact of Esophageal Motion on Dosimetry and Toxicity With Thoracic Radiation Therapy

PURPOSE: To investigate the impact of intra- and inter-fractional esophageal motion on dosimetry and observed toxicity in a phase I dose escalation study of accelerated radiotherapy with concurrent chemotherapy for locally advanced lung cancer. METHODS AND MATERIALS: Patients underwent computed tomo...

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Autores principales: Gao, Hao, Kelsey, Chris R., Boyle, John, Xie, Tianyi, Catalano, Suzanne, Wang, Xiaofei, Yin, Fang-Fang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6537299/
https://www.ncbi.nlm.nih.gov/pubmed/31130076
http://dx.doi.org/10.1177/1533033819849073
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author Gao, Hao
Kelsey, Chris R.
Boyle, John
Xie, Tianyi
Catalano, Suzanne
Wang, Xiaofei
Yin, Fang-Fang
author_facet Gao, Hao
Kelsey, Chris R.
Boyle, John
Xie, Tianyi
Catalano, Suzanne
Wang, Xiaofei
Yin, Fang-Fang
author_sort Gao, Hao
collection PubMed
description PURPOSE: To investigate the impact of intra- and inter-fractional esophageal motion on dosimetry and observed toxicity in a phase I dose escalation study of accelerated radiotherapy with concurrent chemotherapy for locally advanced lung cancer. METHODS AND MATERIALS: Patients underwent computed tomography imaging for radiotherapy treatment planning (CT1 and 4DCT1) and at 2 weeks (CT2 and 4DCT2) and 5 weeks (CT3 and 4DCT3) after initiating treatment. Each computed tomography scan consisted of 10-phase 4DCTs in addition to a static free-breathing or breath-hold computed tomography. The esophagus was independently contoured on all computed tomographies and 4DCTs. Both CT2 and CT3 were rigidly registered with CT1 and doses were recalculated using the original intensity-modulated radiation therapy plan based on CT1 to assess the impact of interfractional motion on esophageal dosimetry. Similarly, 4DCT1 data sets were rigidly registered with CT1 to assess the impact of intrafractional motion. The motion was characterized based on the statistical analysis of slice-by-slice center shifts (after registration) for the upper, middle, and lower esophageal regions, respectively. For the dosimetric analysis, the following quantities were calculated and assessed for correlation with toxicity grade: the percent volumes of esophagus that received at least 20 Gy (V20) and 60 Gy (V60), maximum esophageal dose, equivalent uniform dose, and normal tissue complication probability. RESULTS: The interfractional center shifts were 4.4 ± 1.7 mm, 5.5 ± 2.0 mm and 4.9 ± 2.1 mm for the upper, middle, and lower esophageal regions, respectively, while the intrafractional center shifts were 0.6 ± 0.4 mm, 0.7 ± 0.7 mm, and 0.9 ± 0.7 mm, respectively. The mean V60 (and corresponding normal tissue complication probability) values estimated from the interfractional motion analysis were 7.8% (10%), 4.6% (7.5%), 7.5% (8.6%), and 31% (26%) for grade 0, grade 1, grade 2, and grade 3 toxicities, respectively. CONCLUSIONS: Interfractional esophageal motion is significantly larger than intrafractional motion. The mean values of V60 and corresponding normal tissue complication probability, incorporating interfractional esophageal motion, correlated positively with esophageal toxicity grade.
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spelling pubmed-65372992019-06-14 Impact of Esophageal Motion on Dosimetry and Toxicity With Thoracic Radiation Therapy Gao, Hao Kelsey, Chris R. Boyle, John Xie, Tianyi Catalano, Suzanne Wang, Xiaofei Yin, Fang-Fang Technol Cancer Res Treat Original Article PURPOSE: To investigate the impact of intra- and inter-fractional esophageal motion on dosimetry and observed toxicity in a phase I dose escalation study of accelerated radiotherapy with concurrent chemotherapy for locally advanced lung cancer. METHODS AND MATERIALS: Patients underwent computed tomography imaging for radiotherapy treatment planning (CT1 and 4DCT1) and at 2 weeks (CT2 and 4DCT2) and 5 weeks (CT3 and 4DCT3) after initiating treatment. Each computed tomography scan consisted of 10-phase 4DCTs in addition to a static free-breathing or breath-hold computed tomography. The esophagus was independently contoured on all computed tomographies and 4DCTs. Both CT2 and CT3 were rigidly registered with CT1 and doses were recalculated using the original intensity-modulated radiation therapy plan based on CT1 to assess the impact of interfractional motion on esophageal dosimetry. Similarly, 4DCT1 data sets were rigidly registered with CT1 to assess the impact of intrafractional motion. The motion was characterized based on the statistical analysis of slice-by-slice center shifts (after registration) for the upper, middle, and lower esophageal regions, respectively. For the dosimetric analysis, the following quantities were calculated and assessed for correlation with toxicity grade: the percent volumes of esophagus that received at least 20 Gy (V20) and 60 Gy (V60), maximum esophageal dose, equivalent uniform dose, and normal tissue complication probability. RESULTS: The interfractional center shifts were 4.4 ± 1.7 mm, 5.5 ± 2.0 mm and 4.9 ± 2.1 mm for the upper, middle, and lower esophageal regions, respectively, while the intrafractional center shifts were 0.6 ± 0.4 mm, 0.7 ± 0.7 mm, and 0.9 ± 0.7 mm, respectively. The mean V60 (and corresponding normal tissue complication probability) values estimated from the interfractional motion analysis were 7.8% (10%), 4.6% (7.5%), 7.5% (8.6%), and 31% (26%) for grade 0, grade 1, grade 2, and grade 3 toxicities, respectively. CONCLUSIONS: Interfractional esophageal motion is significantly larger than intrafractional motion. The mean values of V60 and corresponding normal tissue complication probability, incorporating interfractional esophageal motion, correlated positively with esophageal toxicity grade. SAGE Publications 2019-05-26 /pmc/articles/PMC6537299/ /pubmed/31130076 http://dx.doi.org/10.1177/1533033819849073 Text en © The Author(s) 2019 http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Article
Gao, Hao
Kelsey, Chris R.
Boyle, John
Xie, Tianyi
Catalano, Suzanne
Wang, Xiaofei
Yin, Fang-Fang
Impact of Esophageal Motion on Dosimetry and Toxicity With Thoracic Radiation Therapy
title Impact of Esophageal Motion on Dosimetry and Toxicity With Thoracic Radiation Therapy
title_full Impact of Esophageal Motion on Dosimetry and Toxicity With Thoracic Radiation Therapy
title_fullStr Impact of Esophageal Motion on Dosimetry and Toxicity With Thoracic Radiation Therapy
title_full_unstemmed Impact of Esophageal Motion on Dosimetry and Toxicity With Thoracic Radiation Therapy
title_short Impact of Esophageal Motion on Dosimetry and Toxicity With Thoracic Radiation Therapy
title_sort impact of esophageal motion on dosimetry and toxicity with thoracic radiation therapy
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6537299/
https://www.ncbi.nlm.nih.gov/pubmed/31130076
http://dx.doi.org/10.1177/1533033819849073
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