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Feasibility and response of helical tomotherapy in patients with metastatic colorectal cancer

PURPOSE: To investigate the treatment outcome and the toxicity of helical tomotherapy (HT) in patients with metastatic colorectal cancer (mCRC). MATERIALS AND METHODS: We retrospectively reviewed 18 patients with 31 lesions from mCRC treated with HT between 2009 and 2013. The liver (9 lesions) and l...

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Autores principales: Bae, Sun Hyun, Moon, Seong Kwon, Kim, Yong Ho, Cho, Kwang Hwan, Shin, Eung Jin, Lee, Moon Sung, Ryu, Chang Beom, Ko, Bong Min, Yun, Jina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society for Radiation Oncology 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4707215/
https://www.ncbi.nlm.nih.gov/pubmed/26756032
http://dx.doi.org/10.3857/roj.2015.33.4.320
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author Bae, Sun Hyun
Moon, Seong Kwon
Kim, Yong Ho
Cho, Kwang Hwan
Shin, Eung Jin
Lee, Moon Sung
Ryu, Chang Beom
Ko, Bong Min
Yun, Jina
author_facet Bae, Sun Hyun
Moon, Seong Kwon
Kim, Yong Ho
Cho, Kwang Hwan
Shin, Eung Jin
Lee, Moon Sung
Ryu, Chang Beom
Ko, Bong Min
Yun, Jina
author_sort Bae, Sun Hyun
collection PubMed
description PURPOSE: To investigate the treatment outcome and the toxicity of helical tomotherapy (HT) in patients with metastatic colorectal cancer (mCRC). MATERIALS AND METHODS: We retrospectively reviewed 18 patients with 31 lesions from mCRC treated with HT between 2009 and 2013. The liver (9 lesions) and lymph nodes (9 lesions) were the most frequent sites. The planning target volume (PTV) ranged from 12 to 1,110 mL (median, 114 mL). The total doses ranged from 30 to 70 Gy in 10-30 fractions. When the α/β value for the tumor was assumed to be 10 Gy for the biologically equivalent dose (BED), the total doses ranged from 39 to 119 Gy(10) (median, 55 Gy(10)). Nineteen lesions were treated with concurrent chemotherapy (CCRT). RESULTS: With a median follow-up time of 16 months, the median overall survival for 18 patients was 33 months. Eight lesions (26%) achieved complete response. The 1- and 3-year local progression free survival (LPFS) rates for 31 lesions were 45% and 34%, respectively. On univariate analysis, significant parameters influencing LPFS rates were chemotherapy response before HT, aim of HT, CCRT, PTV, BED, and adjuvant chemotherapy. On multivariate analysis, PTV ≤113 mL and BED >48 Gy(10) were associated with a statistically significant improvement in LFPS. During HT, four patients experienced grade 3 hematologic toxicities, each of whom had also received CCRT. CONCLUSION: The current study demonstrates the efficacy and tolerability of HT for mCRC. To define optimal RT dose according to tumor size of mCRC, further study should be needed.
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spelling pubmed-47072152016-01-11 Feasibility and response of helical tomotherapy in patients with metastatic colorectal cancer Bae, Sun Hyun Moon, Seong Kwon Kim, Yong Ho Cho, Kwang Hwan Shin, Eung Jin Lee, Moon Sung Ryu, Chang Beom Ko, Bong Min Yun, Jina Radiat Oncol J Original Article PURPOSE: To investigate the treatment outcome and the toxicity of helical tomotherapy (HT) in patients with metastatic colorectal cancer (mCRC). MATERIALS AND METHODS: We retrospectively reviewed 18 patients with 31 lesions from mCRC treated with HT between 2009 and 2013. The liver (9 lesions) and lymph nodes (9 lesions) were the most frequent sites. The planning target volume (PTV) ranged from 12 to 1,110 mL (median, 114 mL). The total doses ranged from 30 to 70 Gy in 10-30 fractions. When the α/β value for the tumor was assumed to be 10 Gy for the biologically equivalent dose (BED), the total doses ranged from 39 to 119 Gy(10) (median, 55 Gy(10)). Nineteen lesions were treated with concurrent chemotherapy (CCRT). RESULTS: With a median follow-up time of 16 months, the median overall survival for 18 patients was 33 months. Eight lesions (26%) achieved complete response. The 1- and 3-year local progression free survival (LPFS) rates for 31 lesions were 45% and 34%, respectively. On univariate analysis, significant parameters influencing LPFS rates were chemotherapy response before HT, aim of HT, CCRT, PTV, BED, and adjuvant chemotherapy. On multivariate analysis, PTV ≤113 mL and BED >48 Gy(10) were associated with a statistically significant improvement in LFPS. During HT, four patients experienced grade 3 hematologic toxicities, each of whom had also received CCRT. CONCLUSION: The current study demonstrates the efficacy and tolerability of HT for mCRC. To define optimal RT dose according to tumor size of mCRC, further study should be needed. The Korean Society for Radiation Oncology 2015-12 2015-12-30 /pmc/articles/PMC4707215/ /pubmed/26756032 http://dx.doi.org/10.3857/roj.2015.33.4.320 Text en Copyright © 2015. The Korean Society for Radiation Oncology http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Bae, Sun Hyun
Moon, Seong Kwon
Kim, Yong Ho
Cho, Kwang Hwan
Shin, Eung Jin
Lee, Moon Sung
Ryu, Chang Beom
Ko, Bong Min
Yun, Jina
Feasibility and response of helical tomotherapy in patients with metastatic colorectal cancer
title Feasibility and response of helical tomotherapy in patients with metastatic colorectal cancer
title_full Feasibility and response of helical tomotherapy in patients with metastatic colorectal cancer
title_fullStr Feasibility and response of helical tomotherapy in patients with metastatic colorectal cancer
title_full_unstemmed Feasibility and response of helical tomotherapy in patients with metastatic colorectal cancer
title_short Feasibility and response of helical tomotherapy in patients with metastatic colorectal cancer
title_sort feasibility and response of helical tomotherapy in patients with metastatic colorectal cancer
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4707215/
https://www.ncbi.nlm.nih.gov/pubmed/26756032
http://dx.doi.org/10.3857/roj.2015.33.4.320
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