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Comparing the clinical outcomes in stereotactic body radiotherapy for lung tumors between Ray-Tracing and Monte-Carlo algorithms
PURPOSE: The purpose of this study was to compare the clinical outcomes between the groups using Ray-Tracing (RAT) and Monte-Carlo (MC) calculation algorithms for stereotactic body radiotherapy (SBRT) of lung tumors. MATERIALS AND METHODS: Thirty-five patients received SBRT with CyberKnife for 47 pr...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4951350/ https://www.ncbi.nlm.nih.gov/pubmed/26544622 http://dx.doi.org/10.18632/oncotarget.5992 |
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author | Song, Jin Ho Kang, Ki Mun Choi, Hoon-Sik Jeong, Hojin Ha, In Bong Lee, Jong Deog Kim, Ho Cheol Jeong, Yi Yeong Cho, Yu Ji Lee, Seung Jun Kim, Sung Hwan Jang, In-Seok Jeong, Bae Kwon |
author_facet | Song, Jin Ho Kang, Ki Mun Choi, Hoon-Sik Jeong, Hojin Ha, In Bong Lee, Jong Deog Kim, Ho Cheol Jeong, Yi Yeong Cho, Yu Ji Lee, Seung Jun Kim, Sung Hwan Jang, In-Seok Jeong, Bae Kwon |
author_sort | Song, Jin Ho |
collection | PubMed |
description | PURPOSE: The purpose of this study was to compare the clinical outcomes between the groups using Ray-Tracing (RAT) and Monte-Carlo (MC) calculation algorithms for stereotactic body radiotherapy (SBRT) of lung tumors. MATERIALS AND METHODS: Thirty-five patients received SBRT with CyberKnife for 47 primary or metastatic lung tumors. RAT was used for 22 targets in 12 patients, and MC for 25 targets in 23 patients. Total dose of 48 to 60 Gy was prescribed in 3 to 5 fractions on median 80% isodose line. The response rate, local control rate, and toxicities were compared between RAT and MC groups. RESULTS: The response rate was lower in the RAT group (77.3%) compared to the MC group (100%) (p = 0.008). The response rates showed an association with the mean dose to the gross tumor volume, which the doses were re-calculated with MC algorithm in both groups. However, the local control rate and toxicities did not differ between the groups. CONCLUSIONS: The clinical outcome and toxicity of lung SBRT between the RAT and MC groups were similar except for the response rate when the same apparent doses were prescribed. The lower response rate in the RAT group, however, did not compromise the local control rates. As such, reducing the prescription dose for MC algorithm may be performed but done with caution. |
format | Online Article Text |
id | pubmed-4951350 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-49513502016-07-21 Comparing the clinical outcomes in stereotactic body radiotherapy for lung tumors between Ray-Tracing and Monte-Carlo algorithms Song, Jin Ho Kang, Ki Mun Choi, Hoon-Sik Jeong, Hojin Ha, In Bong Lee, Jong Deog Kim, Ho Cheol Jeong, Yi Yeong Cho, Yu Ji Lee, Seung Jun Kim, Sung Hwan Jang, In-Seok Jeong, Bae Kwon Oncotarget Clinical Research Paper PURPOSE: The purpose of this study was to compare the clinical outcomes between the groups using Ray-Tracing (RAT) and Monte-Carlo (MC) calculation algorithms for stereotactic body radiotherapy (SBRT) of lung tumors. MATERIALS AND METHODS: Thirty-five patients received SBRT with CyberKnife for 47 primary or metastatic lung tumors. RAT was used for 22 targets in 12 patients, and MC for 25 targets in 23 patients. Total dose of 48 to 60 Gy was prescribed in 3 to 5 fractions on median 80% isodose line. The response rate, local control rate, and toxicities were compared between RAT and MC groups. RESULTS: The response rate was lower in the RAT group (77.3%) compared to the MC group (100%) (p = 0.008). The response rates showed an association with the mean dose to the gross tumor volume, which the doses were re-calculated with MC algorithm in both groups. However, the local control rate and toxicities did not differ between the groups. CONCLUSIONS: The clinical outcome and toxicity of lung SBRT between the RAT and MC groups were similar except for the response rate when the same apparent doses were prescribed. The lower response rate in the RAT group, however, did not compromise the local control rates. As such, reducing the prescription dose for MC algorithm may be performed but done with caution. Impact Journals LLC 2015-10-26 /pmc/articles/PMC4951350/ /pubmed/26544622 http://dx.doi.org/10.18632/oncotarget.5992 Text en Copyright: © 2016 Song et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Clinical Research Paper Song, Jin Ho Kang, Ki Mun Choi, Hoon-Sik Jeong, Hojin Ha, In Bong Lee, Jong Deog Kim, Ho Cheol Jeong, Yi Yeong Cho, Yu Ji Lee, Seung Jun Kim, Sung Hwan Jang, In-Seok Jeong, Bae Kwon Comparing the clinical outcomes in stereotactic body radiotherapy for lung tumors between Ray-Tracing and Monte-Carlo algorithms |
title | Comparing the clinical outcomes in stereotactic body radiotherapy for lung tumors between Ray-Tracing and Monte-Carlo algorithms |
title_full | Comparing the clinical outcomes in stereotactic body radiotherapy for lung tumors between Ray-Tracing and Monte-Carlo algorithms |
title_fullStr | Comparing the clinical outcomes in stereotactic body radiotherapy for lung tumors between Ray-Tracing and Monte-Carlo algorithms |
title_full_unstemmed | Comparing the clinical outcomes in stereotactic body radiotherapy for lung tumors between Ray-Tracing and Monte-Carlo algorithms |
title_short | Comparing the clinical outcomes in stereotactic body radiotherapy for lung tumors between Ray-Tracing and Monte-Carlo algorithms |
title_sort | comparing the clinical outcomes in stereotactic body radiotherapy for lung tumors between ray-tracing and monte-carlo algorithms |
topic | Clinical Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4951350/ https://www.ncbi.nlm.nih.gov/pubmed/26544622 http://dx.doi.org/10.18632/oncotarget.5992 |
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