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A study of the dosimetric impact of daily setup variations measured with cone‐beam CT on three‐dimensional conformal radiotherapy for early‐stage breast cancer delivered in the prone position

PURPOSE: To evaluate the dosimetric impact of daily positioning variations measured with cone‐beam computed tomography (CBCT) on whole‐breast radiotherapy patients treated in the prone position. METHODS: Daily CBCT was prospectively acquired for 30 consecutive patients positioned prone. Treatment fo...

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Autores principales: Xiao, Annie, Jutzy, Jessica, Hubert, Greg, Edens, Meghan, Washington, Maxine, Hasan, Yasmin, Chmura, Steven J., Al‐Hallaq, Hania A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7769386/
https://www.ncbi.nlm.nih.gov/pubmed/33124774
http://dx.doi.org/10.1002/acm2.13080
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author Xiao, Annie
Jutzy, Jessica
Hubert, Greg
Edens, Meghan
Washington, Maxine
Hasan, Yasmin
Chmura, Steven J.
Al‐Hallaq, Hania A.
author_facet Xiao, Annie
Jutzy, Jessica
Hubert, Greg
Edens, Meghan
Washington, Maxine
Hasan, Yasmin
Chmura, Steven J.
Al‐Hallaq, Hania A.
author_sort Xiao, Annie
collection PubMed
description PURPOSE: To evaluate the dosimetric impact of daily positioning variations measured with cone‐beam computed tomography (CBCT) on whole‐breast radiotherapy patients treated in the prone position. METHODS: Daily CBCT was prospectively acquired for 30 consecutive patients positioned prone. Treatment for early‐stage (≤II) breast cancer was prescribed with standard dose (50 Gy/25 fractions) or hypofractionation (42.56 Gy/16 fractions) for 13 and 17 patients, respectively. Systematic and random errors were calculated from the translational CBCT shifts and used to determine population‐based setup margins. Mean translations (±one standard deviation) for each patient were used to simulate the dosimetric impact on targets (PTV_eval and lumpectomy cavity), heart, and lung. Paired Student’s t tests at α = 0.01 were used to compare dose metrics after correction for multiple testing (P < 0.002). Significant correlation coefficients were used to identify associations (P < 0.01). RESULTS: Of 597 total fractions, 20 ± 13% required patient rotation. Mean translations were 0.29 ± 0.27 cm, 0.41 ± 0.34 cm, and 0.48 ± 0.33 cm in the anterior–posterior, superior–inferior, and lateral directions leading to calculated setup margins of 0.63, 0.88, and 1.10 cm, respectively. Average three‐dimensional (3D) shifts correlated with the maximum distance of breast tissue from the sternum (r = 0.62) but not with body‐mass index. Simulated shifts showed significant, but minor, changes in dose metrics for PTV_eval, lung, and heart. For left‐sided treatments (n = 18), mean heart dose increased from 109 ± 75 cGy to 148 ± 115 cGy. Shifts from the original plan caused PTV_eval hotspots (V105%) to increase by 5.2% ± 3.8%, which correlated with the total MU of wedged fields (r = 0.59). No significant change in V95% to the cavity was found. CONCLUSIONS: Large translational variations that occur when positioning prone breast patients had small but significant dosimetric effects on 3DCRT plans. Daily CBCT may still be necessary to correct for rotational variations that occur in 20% of treatments. To maintain planned dose metrics, unintended beam shifts toward the heart and the contribution of wedged fields should be minimized.
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spelling pubmed-77693862020-12-31 A study of the dosimetric impact of daily setup variations measured with cone‐beam CT on three‐dimensional conformal radiotherapy for early‐stage breast cancer delivered in the prone position Xiao, Annie Jutzy, Jessica Hubert, Greg Edens, Meghan Washington, Maxine Hasan, Yasmin Chmura, Steven J. Al‐Hallaq, Hania A. J Appl Clin Med Phys Radiation Oncology Physics PURPOSE: To evaluate the dosimetric impact of daily positioning variations measured with cone‐beam computed tomography (CBCT) on whole‐breast radiotherapy patients treated in the prone position. METHODS: Daily CBCT was prospectively acquired for 30 consecutive patients positioned prone. Treatment for early‐stage (≤II) breast cancer was prescribed with standard dose (50 Gy/25 fractions) or hypofractionation (42.56 Gy/16 fractions) for 13 and 17 patients, respectively. Systematic and random errors were calculated from the translational CBCT shifts and used to determine population‐based setup margins. Mean translations (±one standard deviation) for each patient were used to simulate the dosimetric impact on targets (PTV_eval and lumpectomy cavity), heart, and lung. Paired Student’s t tests at α = 0.01 were used to compare dose metrics after correction for multiple testing (P < 0.002). Significant correlation coefficients were used to identify associations (P < 0.01). RESULTS: Of 597 total fractions, 20 ± 13% required patient rotation. Mean translations were 0.29 ± 0.27 cm, 0.41 ± 0.34 cm, and 0.48 ± 0.33 cm in the anterior–posterior, superior–inferior, and lateral directions leading to calculated setup margins of 0.63, 0.88, and 1.10 cm, respectively. Average three‐dimensional (3D) shifts correlated with the maximum distance of breast tissue from the sternum (r = 0.62) but not with body‐mass index. Simulated shifts showed significant, but minor, changes in dose metrics for PTV_eval, lung, and heart. For left‐sided treatments (n = 18), mean heart dose increased from 109 ± 75 cGy to 148 ± 115 cGy. Shifts from the original plan caused PTV_eval hotspots (V105%) to increase by 5.2% ± 3.8%, which correlated with the total MU of wedged fields (r = 0.59). No significant change in V95% to the cavity was found. CONCLUSIONS: Large translational variations that occur when positioning prone breast patients had small but significant dosimetric effects on 3DCRT plans. Daily CBCT may still be necessary to correct for rotational variations that occur in 20% of treatments. To maintain planned dose metrics, unintended beam shifts toward the heart and the contribution of wedged fields should be minimized. John Wiley and Sons Inc. 2020-10-30 /pmc/articles/PMC7769386/ /pubmed/33124774 http://dx.doi.org/10.1002/acm2.13080 Text en © 2020 The Authors. Journal of Applied Clinical Medical Physics published by Wiley Periodicals, Inc. on behalf of American Association of Physicists in Medicine This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Radiation Oncology Physics
Xiao, Annie
Jutzy, Jessica
Hubert, Greg
Edens, Meghan
Washington, Maxine
Hasan, Yasmin
Chmura, Steven J.
Al‐Hallaq, Hania A.
A study of the dosimetric impact of daily setup variations measured with cone‐beam CT on three‐dimensional conformal radiotherapy for early‐stage breast cancer delivered in the prone position
title A study of the dosimetric impact of daily setup variations measured with cone‐beam CT on three‐dimensional conformal radiotherapy for early‐stage breast cancer delivered in the prone position
title_full A study of the dosimetric impact of daily setup variations measured with cone‐beam CT on three‐dimensional conformal radiotherapy for early‐stage breast cancer delivered in the prone position
title_fullStr A study of the dosimetric impact of daily setup variations measured with cone‐beam CT on three‐dimensional conformal radiotherapy for early‐stage breast cancer delivered in the prone position
title_full_unstemmed A study of the dosimetric impact of daily setup variations measured with cone‐beam CT on three‐dimensional conformal radiotherapy for early‐stage breast cancer delivered in the prone position
title_short A study of the dosimetric impact of daily setup variations measured with cone‐beam CT on three‐dimensional conformal radiotherapy for early‐stage breast cancer delivered in the prone position
title_sort study of the dosimetric impact of daily setup variations measured with cone‐beam ct on three‐dimensional conformal radiotherapy for early‐stage breast cancer delivered in the prone position
topic Radiation Oncology Physics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7769386/
https://www.ncbi.nlm.nih.gov/pubmed/33124774
http://dx.doi.org/10.1002/acm2.13080
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