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High-dose hypofractionated X-ray radiotherapy for hepatocellular carcinoma: Tumor responses and toxicities

Hypofractionated radiotherapy (RT) has been employed to treat hepatocellular carcinoma (HCC). The present study aimed to report the treatment effects, the dose-response associations and the factors that are associated with radiation-induced liver disease (RILD) in a high-dose hypofractionated RT pro...

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Autores principales: HUANG, BING-SHEN, TSANG, NGAN-MING, LIN, SHI-MING, LIN, DENG-YN, LIEN, JAU-MIN, LIN, CHEN-CHUN, CHEN, WEI-TING, CHEN, WAN-YU, HONG, JI-HONG
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3813808/
https://www.ncbi.nlm.nih.gov/pubmed/24179551
http://dx.doi.org/10.3892/ol.2013.1582
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author HUANG, BING-SHEN
TSANG, NGAN-MING
LIN, SHI-MING
LIN, DENG-YN
LIEN, JAU-MIN
LIN, CHEN-CHUN
CHEN, WEI-TING
CHEN, WAN-YU
HONG, JI-HONG
author_facet HUANG, BING-SHEN
TSANG, NGAN-MING
LIN, SHI-MING
LIN, DENG-YN
LIEN, JAU-MIN
LIN, CHEN-CHUN
CHEN, WEI-TING
CHEN, WAN-YU
HONG, JI-HONG
author_sort HUANG, BING-SHEN
collection PubMed
description Hypofractionated radiotherapy (RT) has been employed to treat hepatocellular carcinoma (HCC). The present study aimed to report the treatment effects, the dose-response associations and the factors that are associated with radiation-induced liver disease (RILD) in a high-dose hypofractionated RT procedure. A total of 40 patients with non-metastatic HCC who underwent RT for local control of irradiated tumors were studied. The treatment technique was that of three-dimensional conformal or intensity-modulated radiation therapy, with a fraction size of 3 Gy and a total dose of 40–66 Gy in 14–23 fractions. The biologically-effective dose (BED) was 52.0–85.8 Gy(10) (median, 74.1 Gy(10)). Tumor regression was observed in 28 patients (70.0%) with a complete response, partial response, stable disease and progressive disease status in 11 (27.5%), 17 (42.5%), five (12.5%) and seven patients (17.5%), respectively. The one-, two- and five-year overall survival (OS) and in-field control (IFC) rates were 60, 40 and 21% and 73, 62 and 56%, respectively. A positive correlation also emerged between the radiation dose and the IFC (P=0.035). Eight of the 40 patients (20%) developed non-classic RILD. A higher Cancer of the Liver Italian Program score was associated with a higher probability of non-classic RILD (P=0.02). The tumor response and IFC rate of HCC following irradiation were significantly dose-dependent. High-dose hypofractionated X-ray RT is a feasible and effective treatment for HCC in patients with good liver function and for those who meet the criteria for a curative attempt.
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spelling pubmed-38138082013-10-31 High-dose hypofractionated X-ray radiotherapy for hepatocellular carcinoma: Tumor responses and toxicities HUANG, BING-SHEN TSANG, NGAN-MING LIN, SHI-MING LIN, DENG-YN LIEN, JAU-MIN LIN, CHEN-CHUN CHEN, WEI-TING CHEN, WAN-YU HONG, JI-HONG Oncol Lett Articles Hypofractionated radiotherapy (RT) has been employed to treat hepatocellular carcinoma (HCC). The present study aimed to report the treatment effects, the dose-response associations and the factors that are associated with radiation-induced liver disease (RILD) in a high-dose hypofractionated RT procedure. A total of 40 patients with non-metastatic HCC who underwent RT for local control of irradiated tumors were studied. The treatment technique was that of three-dimensional conformal or intensity-modulated radiation therapy, with a fraction size of 3 Gy and a total dose of 40–66 Gy in 14–23 fractions. The biologically-effective dose (BED) was 52.0–85.8 Gy(10) (median, 74.1 Gy(10)). Tumor regression was observed in 28 patients (70.0%) with a complete response, partial response, stable disease and progressive disease status in 11 (27.5%), 17 (42.5%), five (12.5%) and seven patients (17.5%), respectively. The one-, two- and five-year overall survival (OS) and in-field control (IFC) rates were 60, 40 and 21% and 73, 62 and 56%, respectively. A positive correlation also emerged between the radiation dose and the IFC (P=0.035). Eight of the 40 patients (20%) developed non-classic RILD. A higher Cancer of the Liver Italian Program score was associated with a higher probability of non-classic RILD (P=0.02). The tumor response and IFC rate of HCC following irradiation were significantly dose-dependent. High-dose hypofractionated X-ray RT is a feasible and effective treatment for HCC in patients with good liver function and for those who meet the criteria for a curative attempt. D.A. Spandidos 2013-11 2013-09-12 /pmc/articles/PMC3813808/ /pubmed/24179551 http://dx.doi.org/10.3892/ol.2013.1582 Text en Copyright © 2013, Spandidos Publications http://creativecommons.org/licenses/by/3.0 This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Articles
HUANG, BING-SHEN
TSANG, NGAN-MING
LIN, SHI-MING
LIN, DENG-YN
LIEN, JAU-MIN
LIN, CHEN-CHUN
CHEN, WEI-TING
CHEN, WAN-YU
HONG, JI-HONG
High-dose hypofractionated X-ray radiotherapy for hepatocellular carcinoma: Tumor responses and toxicities
title High-dose hypofractionated X-ray radiotherapy for hepatocellular carcinoma: Tumor responses and toxicities
title_full High-dose hypofractionated X-ray radiotherapy for hepatocellular carcinoma: Tumor responses and toxicities
title_fullStr High-dose hypofractionated X-ray radiotherapy for hepatocellular carcinoma: Tumor responses and toxicities
title_full_unstemmed High-dose hypofractionated X-ray radiotherapy for hepatocellular carcinoma: Tumor responses and toxicities
title_short High-dose hypofractionated X-ray radiotherapy for hepatocellular carcinoma: Tumor responses and toxicities
title_sort high-dose hypofractionated x-ray radiotherapy for hepatocellular carcinoma: tumor responses and toxicities
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3813808/
https://www.ncbi.nlm.nih.gov/pubmed/24179551
http://dx.doi.org/10.3892/ol.2013.1582
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