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Does CyberKnife Improve Dose Distribution Versus IMRT and VMAT on a Linear Accelerator in Low-risk Prostate Cancer?

BACKGROUND: Hypofractionated stereotactic body radiation therapy (SBRT) for prostate cancer (PCa) can be delivered with the robot-assisted CyberKnife (CK) system or on a linear accelerator using dynamic intensity-modulated radiotherapy (IMRT) or volumetric arc radiotherapy (VMAT). This retrospective...

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Autores principales: Borowicz, Dorota Maria, Skrobała, Agnieszka, Kruszyna-Mochalska, Marta, Malicki, Julian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sciendo 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9122296/
https://www.ncbi.nlm.nih.gov/pubmed/35344646
http://dx.doi.org/10.2478/raon-2022-0010
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author Borowicz, Dorota Maria
Skrobała, Agnieszka
Kruszyna-Mochalska, Marta
Malicki, Julian
author_facet Borowicz, Dorota Maria
Skrobała, Agnieszka
Kruszyna-Mochalska, Marta
Malicki, Julian
author_sort Borowicz, Dorota Maria
collection PubMed
description BACKGROUND: Hypofractionated stereotactic body radiation therapy (SBRT) for prostate cancer (PCa) can be delivered with the robot-assisted CyberKnife (CK) system or on a linear accelerator using dynamic intensity-modulated radiotherapy (IMRT) or volumetric arc radiotherapy (VMAT). This retrospective study was performed to determine whether CK offers better dose distribution than IMRT and/or VMAT. MATERIALS AND METHODS: Treatment plans for three techniques were prepared using the same treatment parameters (36.35 Gy, 7.25 Gy/fr). We evaluated target coverage, conformity index (CI), homogeneity index (HI), gamma index (GI), and organs at risk (OAR) constraints. RESULTS: The mean planning target volume (PTV) dose for CK (39.58 Gy) was significantly greater than VMAT or IMRT (both 36.25 Gy). However, CK resulted in a wider dose range (31.48 to 45.89 Gy) vs. VMAT and IMRT (34.6–38.76 Gy). The mean dose to the rectum (V36Gy, mm(3)) was significantly lower (p < 0.001) in the CK plans (219.78 vs. 519.59 and 422.62, respectively). The mean bladder dose (V37Gy, mm(3)) was significantly greater for CK (3256 vs. 1090.75 for VMAT and 4.5 for IMRT (p < 0.001). CK yielded significantly better CI (1.07 vs. 1.17 and 1.25 for VMAT and IMRT, respectively; p < 0.01) and HI values (1.27 vs. 1.07 and 1.04; p < 0.01). GI values for the δd = 3mm, δ% = 3% criteria were 99.86 (VMAT), 99.07 (IMRT) and 99.99 (CK). For δd = 2mm, δ% = 2%, the corresponding values were 98.3, 93.35, and 97.12, respectively. CONCLUSIONS: For most variables, CK was superior to both VMAT and IMRT. However, dynamic IMRT techniques, especially VMAT, do not differ significantly from CK plans and are therefore acceptable alternatives to CyberKnife.
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spelling pubmed-91222962022-06-01 Does CyberKnife Improve Dose Distribution Versus IMRT and VMAT on a Linear Accelerator in Low-risk Prostate Cancer? Borowicz, Dorota Maria Skrobała, Agnieszka Kruszyna-Mochalska, Marta Malicki, Julian Radiol Oncol Research Article BACKGROUND: Hypofractionated stereotactic body radiation therapy (SBRT) for prostate cancer (PCa) can be delivered with the robot-assisted CyberKnife (CK) system or on a linear accelerator using dynamic intensity-modulated radiotherapy (IMRT) or volumetric arc radiotherapy (VMAT). This retrospective study was performed to determine whether CK offers better dose distribution than IMRT and/or VMAT. MATERIALS AND METHODS: Treatment plans for three techniques were prepared using the same treatment parameters (36.35 Gy, 7.25 Gy/fr). We evaluated target coverage, conformity index (CI), homogeneity index (HI), gamma index (GI), and organs at risk (OAR) constraints. RESULTS: The mean planning target volume (PTV) dose for CK (39.58 Gy) was significantly greater than VMAT or IMRT (both 36.25 Gy). However, CK resulted in a wider dose range (31.48 to 45.89 Gy) vs. VMAT and IMRT (34.6–38.76 Gy). The mean dose to the rectum (V36Gy, mm(3)) was significantly lower (p < 0.001) in the CK plans (219.78 vs. 519.59 and 422.62, respectively). The mean bladder dose (V37Gy, mm(3)) was significantly greater for CK (3256 vs. 1090.75 for VMAT and 4.5 for IMRT (p < 0.001). CK yielded significantly better CI (1.07 vs. 1.17 and 1.25 for VMAT and IMRT, respectively; p < 0.01) and HI values (1.27 vs. 1.07 and 1.04; p < 0.01). GI values for the δd = 3mm, δ% = 3% criteria were 99.86 (VMAT), 99.07 (IMRT) and 99.99 (CK). For δd = 2mm, δ% = 2%, the corresponding values were 98.3, 93.35, and 97.12, respectively. CONCLUSIONS: For most variables, CK was superior to both VMAT and IMRT. However, dynamic IMRT techniques, especially VMAT, do not differ significantly from CK plans and are therefore acceptable alternatives to CyberKnife. Sciendo 2022-03-28 /pmc/articles/PMC9122296/ /pubmed/35344646 http://dx.doi.org/10.2478/raon-2022-0010 Text en © 2022 Dorota Maria Borowicz, Agnieszka Skrobała, Marta Kruszyna-Mochalska, Julian Malicki, published by Sciendo https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under the Creative Commons Attribution 4.0 International License.
spellingShingle Research Article
Borowicz, Dorota Maria
Skrobała, Agnieszka
Kruszyna-Mochalska, Marta
Malicki, Julian
Does CyberKnife Improve Dose Distribution Versus IMRT and VMAT on a Linear Accelerator in Low-risk Prostate Cancer?
title Does CyberKnife Improve Dose Distribution Versus IMRT and VMAT on a Linear Accelerator in Low-risk Prostate Cancer?
title_full Does CyberKnife Improve Dose Distribution Versus IMRT and VMAT on a Linear Accelerator in Low-risk Prostate Cancer?
title_fullStr Does CyberKnife Improve Dose Distribution Versus IMRT and VMAT on a Linear Accelerator in Low-risk Prostate Cancer?
title_full_unstemmed Does CyberKnife Improve Dose Distribution Versus IMRT and VMAT on a Linear Accelerator in Low-risk Prostate Cancer?
title_short Does CyberKnife Improve Dose Distribution Versus IMRT and VMAT on a Linear Accelerator in Low-risk Prostate Cancer?
title_sort does cyberknife improve dose distribution versus imrt and vmat on a linear accelerator in low-risk prostate cancer?
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9122296/
https://www.ncbi.nlm.nih.gov/pubmed/35344646
http://dx.doi.org/10.2478/raon-2022-0010
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