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Establishment of linear accelerator-based image guided radiotherapy for orthotopic 4T1 mouse mammary tumor model

This study was conducted to assess the feasibility of image guided radiotherapy (IGRT) for orthotopic 4T1 mouse mammary tumor using linear accelerator (LINAC). Eighteen Balb/C mice were inoculated with 4T1 cells on left mammary fat pad and nine of them were irradiated using LINAC. Tumors, planning t...

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Autores principales: Lee, Seung-Heon, Kim, Ji-Young, Lee, Kyu-Chan, Nam, Jeong-Seok, Choi, Jinho, Lee, Seok-Ho, Sung, Ki-Hoon, Ahn, So-Hyun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Association for Laboratory Animal Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4079833/
https://www.ncbi.nlm.nih.gov/pubmed/24999360
http://dx.doi.org/10.5625/lar.2014.30.2.64
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author Lee, Seung-Heon
Kim, Ji-Young
Lee, Kyu-Chan
Nam, Jeong-Seok
Choi, Jinho
Lee, Seok-Ho
Sung, Ki-Hoon
Ahn, So-Hyun
author_facet Lee, Seung-Heon
Kim, Ji-Young
Lee, Kyu-Chan
Nam, Jeong-Seok
Choi, Jinho
Lee, Seok-Ho
Sung, Ki-Hoon
Ahn, So-Hyun
author_sort Lee, Seung-Heon
collection PubMed
description This study was conducted to assess the feasibility of image guided radiotherapy (IGRT) for orthotopic 4T1 mouse mammary tumor using linear accelerator (LINAC). Eighteen Balb/C mice were inoculated with 4T1 cells on left mammary fat pad and nine of them were irradiated using LINAC. Tumors, planning target volumes (PTV), bowels adjacent to tumors, bones and lungs were delineated on planning CT images. IGRT plans were generated to irradiate prescription dose to at least 90% of the PTV and then compared with conventional 2-dimensional plans with anterior-posterior and posterior-anterior beams with 5 mm margins (2D AP/PA plan). Homemade dose-build-up-cradle was designed to encompass mouse bed for homogeneous dose build up. To confirm the irradiated dose, tumor doses were measured using diode detector placed on the surface of tumors. Plan comparison demonstrated equivalent doses to PTV while sparing more doses to normal tissues including bowel (from 90.9% to 40.5%, median value of mean doses) and bone marrow (from 12.9% to 4.7%, median value of mean doses) than 2D AP/PA plan. Quality assurance using diode detector confirmed that IGRT could deliver 95.3-105.3% of the planned doses to PTV. Tumors grew 505.2-1185.8% (mean 873.3%) in the control group and 436.1-771.8% (mean 615.5%) in the irradiated group. These results demonstrate that LINAC-based IGRT provides a reliable approach with accurate dose delivery in the radiobiological study for orthotropic tumor model maintaining tumor microenvironment.
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spelling pubmed-40798332014-07-04 Establishment of linear accelerator-based image guided radiotherapy for orthotopic 4T1 mouse mammary tumor model Lee, Seung-Heon Kim, Ji-Young Lee, Kyu-Chan Nam, Jeong-Seok Choi, Jinho Lee, Seok-Ho Sung, Ki-Hoon Ahn, So-Hyun Lab Anim Res Original Article This study was conducted to assess the feasibility of image guided radiotherapy (IGRT) for orthotopic 4T1 mouse mammary tumor using linear accelerator (LINAC). Eighteen Balb/C mice were inoculated with 4T1 cells on left mammary fat pad and nine of them were irradiated using LINAC. Tumors, planning target volumes (PTV), bowels adjacent to tumors, bones and lungs were delineated on planning CT images. IGRT plans were generated to irradiate prescription dose to at least 90% of the PTV and then compared with conventional 2-dimensional plans with anterior-posterior and posterior-anterior beams with 5 mm margins (2D AP/PA plan). Homemade dose-build-up-cradle was designed to encompass mouse bed for homogeneous dose build up. To confirm the irradiated dose, tumor doses were measured using diode detector placed on the surface of tumors. Plan comparison demonstrated equivalent doses to PTV while sparing more doses to normal tissues including bowel (from 90.9% to 40.5%, median value of mean doses) and bone marrow (from 12.9% to 4.7%, median value of mean doses) than 2D AP/PA plan. Quality assurance using diode detector confirmed that IGRT could deliver 95.3-105.3% of the planned doses to PTV. Tumors grew 505.2-1185.8% (mean 873.3%) in the control group and 436.1-771.8% (mean 615.5%) in the irradiated group. These results demonstrate that LINAC-based IGRT provides a reliable approach with accurate dose delivery in the radiobiological study for orthotropic tumor model maintaining tumor microenvironment. Korean Association for Laboratory Animal Science 2014-06 2014-06-23 /pmc/articles/PMC4079833/ /pubmed/24999360 http://dx.doi.org/10.5625/lar.2014.30.2.64 Text en Copyright © 2014 Korean Association for Laboratory Animal Science http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Lee, Seung-Heon
Kim, Ji-Young
Lee, Kyu-Chan
Nam, Jeong-Seok
Choi, Jinho
Lee, Seok-Ho
Sung, Ki-Hoon
Ahn, So-Hyun
Establishment of linear accelerator-based image guided radiotherapy for orthotopic 4T1 mouse mammary tumor model
title Establishment of linear accelerator-based image guided radiotherapy for orthotopic 4T1 mouse mammary tumor model
title_full Establishment of linear accelerator-based image guided radiotherapy for orthotopic 4T1 mouse mammary tumor model
title_fullStr Establishment of linear accelerator-based image guided radiotherapy for orthotopic 4T1 mouse mammary tumor model
title_full_unstemmed Establishment of linear accelerator-based image guided radiotherapy for orthotopic 4T1 mouse mammary tumor model
title_short Establishment of linear accelerator-based image guided radiotherapy for orthotopic 4T1 mouse mammary tumor model
title_sort establishment of linear accelerator-based image guided radiotherapy for orthotopic 4t1 mouse mammary tumor model
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4079833/
https://www.ncbi.nlm.nih.gov/pubmed/24999360
http://dx.doi.org/10.5625/lar.2014.30.2.64
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