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Effect of CyberKnife stereotactic body radiation therapy for hepatocellular carcinoma on hepatic toxicity

OBJECTIVE: To evaluate the safety of CyberKnife stereotactic body radiation therapy (SBRT) for hepatocellular carcinoma (HCC) patients and identify the treatment-related risk factors of hepatic toxicity. MATERIALS AND METHODS: One hundred and four HCC patients treated with CyberKnife SBRT were inclu...

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Autores principales: Liang, Ping, Huang, Cheng, Liang, Shi-Xiong, Li, Ye-Fei, Huang, Shang-Xiao, Lian, Zu-Ping, Liu, Jian-Min, Tang, Yang, Lu, Hai-Jie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5125791/
https://www.ncbi.nlm.nih.gov/pubmed/27920555
http://dx.doi.org/10.2147/OTT.S112290
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author Liang, Ping
Huang, Cheng
Liang, Shi-Xiong
Li, Ye-Fei
Huang, Shang-Xiao
Lian, Zu-Ping
Liu, Jian-Min
Tang, Yang
Lu, Hai-Jie
author_facet Liang, Ping
Huang, Cheng
Liang, Shi-Xiong
Li, Ye-Fei
Huang, Shang-Xiao
Lian, Zu-Ping
Liu, Jian-Min
Tang, Yang
Lu, Hai-Jie
author_sort Liang, Ping
collection PubMed
description OBJECTIVE: To evaluate the safety of CyberKnife stereotactic body radiation therapy (SBRT) for hepatocellular carcinoma (HCC) patients and identify the treatment-related risk factors of hepatic toxicity. MATERIALS AND METHODS: One hundred and four HCC patients treated with CyberKnife SBRT were included in this study between August 2009 and December 2012. The average dose of prescribed radiation was 42.81±4.78 Gy (28–55 Gy) with the average fraction size of 8–16 Gy to the planning target volume. The average fractions were 3.31±0.81 (2–6 fractions). Response rates were determined, and the Child–Pugh (CP) score and class following CyberKnife SBRT were obtained to evaluate hepatic toxicity. RESULTS: Seventeen patients experienced progression in CP class and 24 patients experienced CTCAE V. 4.0 grade 2–3 hepatic toxicity during the five-month follow-up period, while no patient experienced grade 4 liver toxicity. Multivariate analysis indicated that only V(25) was an independent factor in grade 2–3 hepatic toxicity (P=0.029, <0.05). Radiation-induced hepatic toxicity (RIHT), defined as an increase of at least two points within three months following CyberKnife SBRT, occurred in 13 of the 104 patients (13/104, 12.5%), and only the normal liver tissue was found to be associated with RIHT (P=0.008, <0.05). CONCLUSION: CyberKnife SBRT is a feasible and safe treatment for HCC with regard to hepatic toxicity, while V(25) and normal liver volume may be an independent factor of grade 2–3 hepatic toxicity and RIHT, respectively.
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spelling pubmed-51257912016-12-05 Effect of CyberKnife stereotactic body radiation therapy for hepatocellular carcinoma on hepatic toxicity Liang, Ping Huang, Cheng Liang, Shi-Xiong Li, Ye-Fei Huang, Shang-Xiao Lian, Zu-Ping Liu, Jian-Min Tang, Yang Lu, Hai-Jie Onco Targets Ther Original Research OBJECTIVE: To evaluate the safety of CyberKnife stereotactic body radiation therapy (SBRT) for hepatocellular carcinoma (HCC) patients and identify the treatment-related risk factors of hepatic toxicity. MATERIALS AND METHODS: One hundred and four HCC patients treated with CyberKnife SBRT were included in this study between August 2009 and December 2012. The average dose of prescribed radiation was 42.81±4.78 Gy (28–55 Gy) with the average fraction size of 8–16 Gy to the planning target volume. The average fractions were 3.31±0.81 (2–6 fractions). Response rates were determined, and the Child–Pugh (CP) score and class following CyberKnife SBRT were obtained to evaluate hepatic toxicity. RESULTS: Seventeen patients experienced progression in CP class and 24 patients experienced CTCAE V. 4.0 grade 2–3 hepatic toxicity during the five-month follow-up period, while no patient experienced grade 4 liver toxicity. Multivariate analysis indicated that only V(25) was an independent factor in grade 2–3 hepatic toxicity (P=0.029, <0.05). Radiation-induced hepatic toxicity (RIHT), defined as an increase of at least two points within three months following CyberKnife SBRT, occurred in 13 of the 104 patients (13/104, 12.5%), and only the normal liver tissue was found to be associated with RIHT (P=0.008, <0.05). CONCLUSION: CyberKnife SBRT is a feasible and safe treatment for HCC with regard to hepatic toxicity, while V(25) and normal liver volume may be an independent factor of grade 2–3 hepatic toxicity and RIHT, respectively. Dove Medical Press 2016-11-18 /pmc/articles/PMC5125791/ /pubmed/27920555 http://dx.doi.org/10.2147/OTT.S112290 Text en © 2016 Liang et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Liang, Ping
Huang, Cheng
Liang, Shi-Xiong
Li, Ye-Fei
Huang, Shang-Xiao
Lian, Zu-Ping
Liu, Jian-Min
Tang, Yang
Lu, Hai-Jie
Effect of CyberKnife stereotactic body radiation therapy for hepatocellular carcinoma on hepatic toxicity
title Effect of CyberKnife stereotactic body radiation therapy for hepatocellular carcinoma on hepatic toxicity
title_full Effect of CyberKnife stereotactic body radiation therapy for hepatocellular carcinoma on hepatic toxicity
title_fullStr Effect of CyberKnife stereotactic body radiation therapy for hepatocellular carcinoma on hepatic toxicity
title_full_unstemmed Effect of CyberKnife stereotactic body radiation therapy for hepatocellular carcinoma on hepatic toxicity
title_short Effect of CyberKnife stereotactic body radiation therapy for hepatocellular carcinoma on hepatic toxicity
title_sort effect of cyberknife stereotactic body radiation therapy for hepatocellular carcinoma on hepatic toxicity
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5125791/
https://www.ncbi.nlm.nih.gov/pubmed/27920555
http://dx.doi.org/10.2147/OTT.S112290
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