Cargando…

A Model for Estimating Dose-Rate Effects on Cell-Killing of Human Melanoma after Boron Neutron Capture Therapy

Boron neutron capture therapy (BNCT) is a type of radiation therapy for eradicating tumor cells through a (10)B(n,α)(7)Li reaction in the presence of (10)B in cancer cells. When delivering a high absorbed dose to cancer cells using BNCT, both the timeline of (10)B concentrations and the relative lon...

Descripción completa

Detalles Bibliográficos
Autores principales: Matsuya, Yusuke, Fukunaga, Hisanori, Omura, Motoko, Date, Hiroyuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7290789/
https://www.ncbi.nlm.nih.gov/pubmed/32365916
http://dx.doi.org/10.3390/cells9051117
_version_ 1783545758556880896
author Matsuya, Yusuke
Fukunaga, Hisanori
Omura, Motoko
Date, Hiroyuki
author_facet Matsuya, Yusuke
Fukunaga, Hisanori
Omura, Motoko
Date, Hiroyuki
author_sort Matsuya, Yusuke
collection PubMed
description Boron neutron capture therapy (BNCT) is a type of radiation therapy for eradicating tumor cells through a (10)B(n,α)(7)Li reaction in the presence of (10)B in cancer cells. When delivering a high absorbed dose to cancer cells using BNCT, both the timeline of (10)B concentrations and the relative long dose-delivery time compared to photon therapy must be considered. Changes in radiosensitivity during such a long dose-delivery time can reduce the probability of tumor control; however, such changes have not yet been evaluated. Here, we propose an improved integrated microdosimetric-kinetic model that accounts for changes in microdosimetric quantities and dose rates depending on the (10)B concentration and investigate the cell recovery (dose-rate effects) of melanoma during BNCT irradiation. The integrated microdosimetric–kinetic model used in this study considers both sub-lethal damage repair and changes in microdosimetric quantities during irradiation. The model, coupled with the Monte Carlo track structure simulation code of the Particle and Heavy Ion Transport code System, shows good agreement with in vitro experimental data for acute exposure to (60)Co γ-rays, thermal neutrons, and BNCT with (10)B concentrations of 10 ppm. This indicates that microdosimetric quantities are important parameters for predicting dose-response curves for cell survival under BNCT irradiations. Furthermore, the model estimation at the endpoint of the mean activation dose exhibits a reduced impact of cell recovery during BNCT irradiations with high linear energy transfer (LET) compared to (60)Co γ-rays irradiation with low LET. Throughout this study, we discuss the advantages of BNCT for enhancing the killing of cancer cells with a reduced dose-rate dependency. If the neutron spectrum and the timelines for drug and dose delivery are provided, the present model will make it possible to predict radiosensitivity for more realistic dose-delivery schemes in BNCT irradiations.
format Online
Article
Text
id pubmed-7290789
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-72907892020-06-17 A Model for Estimating Dose-Rate Effects on Cell-Killing of Human Melanoma after Boron Neutron Capture Therapy Matsuya, Yusuke Fukunaga, Hisanori Omura, Motoko Date, Hiroyuki Cells Article Boron neutron capture therapy (BNCT) is a type of radiation therapy for eradicating tumor cells through a (10)B(n,α)(7)Li reaction in the presence of (10)B in cancer cells. When delivering a high absorbed dose to cancer cells using BNCT, both the timeline of (10)B concentrations and the relative long dose-delivery time compared to photon therapy must be considered. Changes in radiosensitivity during such a long dose-delivery time can reduce the probability of tumor control; however, such changes have not yet been evaluated. Here, we propose an improved integrated microdosimetric-kinetic model that accounts for changes in microdosimetric quantities and dose rates depending on the (10)B concentration and investigate the cell recovery (dose-rate effects) of melanoma during BNCT irradiation. The integrated microdosimetric–kinetic model used in this study considers both sub-lethal damage repair and changes in microdosimetric quantities during irradiation. The model, coupled with the Monte Carlo track structure simulation code of the Particle and Heavy Ion Transport code System, shows good agreement with in vitro experimental data for acute exposure to (60)Co γ-rays, thermal neutrons, and BNCT with (10)B concentrations of 10 ppm. This indicates that microdosimetric quantities are important parameters for predicting dose-response curves for cell survival under BNCT irradiations. Furthermore, the model estimation at the endpoint of the mean activation dose exhibits a reduced impact of cell recovery during BNCT irradiations with high linear energy transfer (LET) compared to (60)Co γ-rays irradiation with low LET. Throughout this study, we discuss the advantages of BNCT for enhancing the killing of cancer cells with a reduced dose-rate dependency. If the neutron spectrum and the timelines for drug and dose delivery are provided, the present model will make it possible to predict radiosensitivity for more realistic dose-delivery schemes in BNCT irradiations. MDPI 2020-04-30 /pmc/articles/PMC7290789/ /pubmed/32365916 http://dx.doi.org/10.3390/cells9051117 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Matsuya, Yusuke
Fukunaga, Hisanori
Omura, Motoko
Date, Hiroyuki
A Model for Estimating Dose-Rate Effects on Cell-Killing of Human Melanoma after Boron Neutron Capture Therapy
title A Model for Estimating Dose-Rate Effects on Cell-Killing of Human Melanoma after Boron Neutron Capture Therapy
title_full A Model for Estimating Dose-Rate Effects on Cell-Killing of Human Melanoma after Boron Neutron Capture Therapy
title_fullStr A Model for Estimating Dose-Rate Effects on Cell-Killing of Human Melanoma after Boron Neutron Capture Therapy
title_full_unstemmed A Model for Estimating Dose-Rate Effects on Cell-Killing of Human Melanoma after Boron Neutron Capture Therapy
title_short A Model for Estimating Dose-Rate Effects on Cell-Killing of Human Melanoma after Boron Neutron Capture Therapy
title_sort model for estimating dose-rate effects on cell-killing of human melanoma after boron neutron capture therapy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7290789/
https://www.ncbi.nlm.nih.gov/pubmed/32365916
http://dx.doi.org/10.3390/cells9051117
work_keys_str_mv AT matsuyayusuke amodelforestimatingdoserateeffectsoncellkillingofhumanmelanomaafterboronneutroncapturetherapy
AT fukunagahisanori amodelforestimatingdoserateeffectsoncellkillingofhumanmelanomaafterboronneutroncapturetherapy
AT omuramotoko amodelforestimatingdoserateeffectsoncellkillingofhumanmelanomaafterboronneutroncapturetherapy
AT datehiroyuki amodelforestimatingdoserateeffectsoncellkillingofhumanmelanomaafterboronneutroncapturetherapy
AT matsuyayusuke modelforestimatingdoserateeffectsoncellkillingofhumanmelanomaafterboronneutroncapturetherapy
AT fukunagahisanori modelforestimatingdoserateeffectsoncellkillingofhumanmelanomaafterboronneutroncapturetherapy
AT omuramotoko modelforestimatingdoserateeffectsoncellkillingofhumanmelanomaafterboronneutroncapturetherapy
AT datehiroyuki modelforestimatingdoserateeffectsoncellkillingofhumanmelanomaafterboronneutroncapturetherapy