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A dosimetric evaluation of VMAT for the treatment of non‐small cell lung cancer

The purpose of this study was to demonstrate the dosimetric potential of volumetric‐modulated arc therapy (VMAT) for the treatment of patients with medically inoperable stage I/II non‐small cell lung cancer (NSCLC) with stereotactic body radiation therapy (SBRT). Fourteen patients treated with 3D CR...

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Autores principales: Merrow, Caitlin E., Wang, Iris Z., Podgorsak, Matthew B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5714051/
https://www.ncbi.nlm.nih.gov/pubmed/23318374
http://dx.doi.org/10.1120/jacmp.v14i1.4110
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author Merrow, Caitlin E.
Wang, Iris Z.
Podgorsak, Matthew B.
author_facet Merrow, Caitlin E.
Wang, Iris Z.
Podgorsak, Matthew B.
author_sort Merrow, Caitlin E.
collection PubMed
description The purpose of this study was to demonstrate the dosimetric potential of volumetric‐modulated arc therapy (VMAT) for the treatment of patients with medically inoperable stage I/II non‐small cell lung cancer (NSCLC) with stereotactic body radiation therapy (SBRT). Fourteen patients treated with 3D CRT with varying tumor locations, tumor sizes, and dose fractionation schemes were chosen for study. The prescription doses were 48 Gy in 4 fractions, 52.5 Gy in 5 fractions, 57.5 Gy in 5 fractions, and 60 Gy in 3 fractions for 2, 5, 1, and 6 patients, respectively. VMAT treatment plans with a mix of two to three full and partial noncoplanar arcs with 5°–25° separations were retrospectively generated using Eclipse version 10.0. The 3D CRT and VMAT plans were then evaluated by comparing their target dose, critical structure dose, high dose spillage, and low dose spillage as defined according to RTOG 0813 and RTOG 0236 protocols. In the most dosimetrically improved case, VMAT was able to decrease the dose from 17.35 Gy to 1.54 Gy to the heart. The [Formula: see text] decreased in 11 of 14 cases when using VMAT. The three that worsened were still within the acceptance criteria. Of the 14 3D CRT plans, seven had a [Formula: see text] minor deviation, while only one of the 14 VMAT plans had a [Formula: see text] minor deviation. The [Formula: see text] improved in 13 of the 14 VMAT cases. The one case that worsened was still within the acceptance criteria of the RTOG protocol. Of the 14 3D CRT plans, seven had an [Formula: see text] deviation. Only one of the 14 VMAT plans had an [Formula: see text] deviation, but it was still improved compared to the 3D CRT plan. In this cohort of patients, no evident dosimetric compromises resulted from planning SBRT treatments with VMAT relative to the 3D CRT treatment plans actually used in their treatment. PACS numbers: 87.50.‐a, 87.53.‐j, 87.55.‐x, 87.55.D‐, 87.55.dk, 87.55.de
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spelling pubmed-57140512018-04-02 A dosimetric evaluation of VMAT for the treatment of non‐small cell lung cancer Merrow, Caitlin E. Wang, Iris Z. Podgorsak, Matthew B. J Appl Clin Med Phys Radiation Oncology Physics The purpose of this study was to demonstrate the dosimetric potential of volumetric‐modulated arc therapy (VMAT) for the treatment of patients with medically inoperable stage I/II non‐small cell lung cancer (NSCLC) with stereotactic body radiation therapy (SBRT). Fourteen patients treated with 3D CRT with varying tumor locations, tumor sizes, and dose fractionation schemes were chosen for study. The prescription doses were 48 Gy in 4 fractions, 52.5 Gy in 5 fractions, 57.5 Gy in 5 fractions, and 60 Gy in 3 fractions for 2, 5, 1, and 6 patients, respectively. VMAT treatment plans with a mix of two to three full and partial noncoplanar arcs with 5°–25° separations were retrospectively generated using Eclipse version 10.0. The 3D CRT and VMAT plans were then evaluated by comparing their target dose, critical structure dose, high dose spillage, and low dose spillage as defined according to RTOG 0813 and RTOG 0236 protocols. In the most dosimetrically improved case, VMAT was able to decrease the dose from 17.35 Gy to 1.54 Gy to the heart. The [Formula: see text] decreased in 11 of 14 cases when using VMAT. The three that worsened were still within the acceptance criteria. Of the 14 3D CRT plans, seven had a [Formula: see text] minor deviation, while only one of the 14 VMAT plans had a [Formula: see text] minor deviation. The [Formula: see text] improved in 13 of the 14 VMAT cases. The one case that worsened was still within the acceptance criteria of the RTOG protocol. Of the 14 3D CRT plans, seven had an [Formula: see text] deviation. Only one of the 14 VMAT plans had an [Formula: see text] deviation, but it was still improved compared to the 3D CRT plan. In this cohort of patients, no evident dosimetric compromises resulted from planning SBRT treatments with VMAT relative to the 3D CRT treatment plans actually used in their treatment. PACS numbers: 87.50.‐a, 87.53.‐j, 87.55.‐x, 87.55.D‐, 87.55.dk, 87.55.de John Wiley and Sons Inc. 2012-09-01 /pmc/articles/PMC5714051/ /pubmed/23318374 http://dx.doi.org/10.1120/jacmp.v14i1.4110 Text en © 2013 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
Merrow, Caitlin E.
Wang, Iris Z.
Podgorsak, Matthew B.
A dosimetric evaluation of VMAT for the treatment of non‐small cell lung cancer
title A dosimetric evaluation of VMAT for the treatment of non‐small cell lung cancer
title_full A dosimetric evaluation of VMAT for the treatment of non‐small cell lung cancer
title_fullStr A dosimetric evaluation of VMAT for the treatment of non‐small cell lung cancer
title_full_unstemmed A dosimetric evaluation of VMAT for the treatment of non‐small cell lung cancer
title_short A dosimetric evaluation of VMAT for the treatment of non‐small cell lung cancer
title_sort dosimetric evaluation of vmat for the treatment of non‐small cell lung cancer
topic Radiation Oncology Physics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5714051/
https://www.ncbi.nlm.nih.gov/pubmed/23318374
http://dx.doi.org/10.1120/jacmp.v14i1.4110
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