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Ultra-Hypofractionated Proton Therapy in Localized Prostate Cancer: Passive Scattering versus Intensity-Modulated Proton Therapy

Few studies have directly compared passive scattering (PS) to intensity-modulated proton therapy (IMPT) in the delivery of ultra-hypofractionated proton beams to the localized prostate cancer (PCa). In this preliminary study involving five patients previously treated with CyberKnife, treatment plans...

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Autores principales: Borowicz, Dorota Maria, Shipulin, Konstantin N., Mytsin, Gennady V., Skrobała, Agnieszka, Milecki, Piotr, Gayevsky, Victor N., Vondráček, Vladimir, Malicki, Julian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8709262/
https://www.ncbi.nlm.nih.gov/pubmed/34945783
http://dx.doi.org/10.3390/jpm11121311
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author Borowicz, Dorota Maria
Shipulin, Konstantin N.
Mytsin, Gennady V.
Skrobała, Agnieszka
Milecki, Piotr
Gayevsky, Victor N.
Vondráček, Vladimir
Malicki, Julian
author_facet Borowicz, Dorota Maria
Shipulin, Konstantin N.
Mytsin, Gennady V.
Skrobała, Agnieszka
Milecki, Piotr
Gayevsky, Victor N.
Vondráček, Vladimir
Malicki, Julian
author_sort Borowicz, Dorota Maria
collection PubMed
description Few studies have directly compared passive scattering (PS) to intensity-modulated proton therapy (IMPT) in the delivery of ultra-hypofractionated proton beams to the localized prostate cancer (PCa). In this preliminary study involving five patients previously treated with CyberKnife, treatment plans were created for PS and IMPT (36.25 CGE in five fractions with two opposing fields) to compare the dosimetric parameters to the planning target volume (PTV) and organs-at-risk (OAR: rectum, bladder, femoral heads). Both plans met the acceptance criteria. Significant differences were observed in the minimum and maximum doses to the PTV. The mean dose to the PTV was lower for PS (35.62 ± 0.26 vs. 37.18 ± 0.14; p = 0.002). Target coverage (D98%) was better for IMPT (96.79% vs. 99.10%; p = 0.004). IMPT resulted in significantly lower mean doses to the rectum (16.75 CGE vs. 6.88 CGE; p = 0.004) and bladder (17.69 CGE vs. 5.98 CGE p = 0.002). High dose to the rectum (V36.25 CGE) were lower with PS, but not significantly opposite to high dose to the bladder. No significant differences were observed in mean conformity index values, with a non-significant trend towards higher mean homogeneity index values for PS. Non-significant differences in the gamma index for both fields were observed. These findings suggest that both PS and IMPT ultra-hypofractionated proton therapy for PCa are highly precise, offering good target coverage and sparing of normal tissues and OARs.
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spelling pubmed-87092622021-12-25 Ultra-Hypofractionated Proton Therapy in Localized Prostate Cancer: Passive Scattering versus Intensity-Modulated Proton Therapy Borowicz, Dorota Maria Shipulin, Konstantin N. Mytsin, Gennady V. Skrobała, Agnieszka Milecki, Piotr Gayevsky, Victor N. Vondráček, Vladimir Malicki, Julian J Pers Med Article Few studies have directly compared passive scattering (PS) to intensity-modulated proton therapy (IMPT) in the delivery of ultra-hypofractionated proton beams to the localized prostate cancer (PCa). In this preliminary study involving five patients previously treated with CyberKnife, treatment plans were created for PS and IMPT (36.25 CGE in five fractions with two opposing fields) to compare the dosimetric parameters to the planning target volume (PTV) and organs-at-risk (OAR: rectum, bladder, femoral heads). Both plans met the acceptance criteria. Significant differences were observed in the minimum and maximum doses to the PTV. The mean dose to the PTV was lower for PS (35.62 ± 0.26 vs. 37.18 ± 0.14; p = 0.002). Target coverage (D98%) was better for IMPT (96.79% vs. 99.10%; p = 0.004). IMPT resulted in significantly lower mean doses to the rectum (16.75 CGE vs. 6.88 CGE; p = 0.004) and bladder (17.69 CGE vs. 5.98 CGE p = 0.002). High dose to the rectum (V36.25 CGE) were lower with PS, but not significantly opposite to high dose to the bladder. No significant differences were observed in mean conformity index values, with a non-significant trend towards higher mean homogeneity index values for PS. Non-significant differences in the gamma index for both fields were observed. These findings suggest that both PS and IMPT ultra-hypofractionated proton therapy for PCa are highly precise, offering good target coverage and sparing of normal tissues and OARs. MDPI 2021-12-06 /pmc/articles/PMC8709262/ /pubmed/34945783 http://dx.doi.org/10.3390/jpm11121311 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Borowicz, Dorota Maria
Shipulin, Konstantin N.
Mytsin, Gennady V.
Skrobała, Agnieszka
Milecki, Piotr
Gayevsky, Victor N.
Vondráček, Vladimir
Malicki, Julian
Ultra-Hypofractionated Proton Therapy in Localized Prostate Cancer: Passive Scattering versus Intensity-Modulated Proton Therapy
title Ultra-Hypofractionated Proton Therapy in Localized Prostate Cancer: Passive Scattering versus Intensity-Modulated Proton Therapy
title_full Ultra-Hypofractionated Proton Therapy in Localized Prostate Cancer: Passive Scattering versus Intensity-Modulated Proton Therapy
title_fullStr Ultra-Hypofractionated Proton Therapy in Localized Prostate Cancer: Passive Scattering versus Intensity-Modulated Proton Therapy
title_full_unstemmed Ultra-Hypofractionated Proton Therapy in Localized Prostate Cancer: Passive Scattering versus Intensity-Modulated Proton Therapy
title_short Ultra-Hypofractionated Proton Therapy in Localized Prostate Cancer: Passive Scattering versus Intensity-Modulated Proton Therapy
title_sort ultra-hypofractionated proton therapy in localized prostate cancer: passive scattering versus intensity-modulated proton therapy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8709262/
https://www.ncbi.nlm.nih.gov/pubmed/34945783
http://dx.doi.org/10.3390/jpm11121311
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