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Palliative Liver Radiotherapy (RT) for Symptomatic Hepatocellular Carcinoma (HCC)

This study aims at evaluating the symptom response, response duration, and toxicity of single dose palliative liver radiotherapy (RT) for symptomatic HCC patients. We reviewed unresectable HCC patients treated with palliative RT in our institution. Eligible patients were unsuitable or refractory to...

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Autores principales: Yeung, Cynthia S. Y., Chiang, C. L., Wong, Natalie S. M., Ha, S. K., Tsang, K. S., Ho, Connie H. M., Wang, B., Lee, Venus W. Y., Chan, Mark K. H., Lee, Francis A. S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6985173/
https://www.ncbi.nlm.nih.gov/pubmed/31988376
http://dx.doi.org/10.1038/s41598-020-58108-1
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author Yeung, Cynthia S. Y.
Chiang, C. L.
Wong, Natalie S. M.
Ha, S. K.
Tsang, K. S.
Ho, Connie H. M.
Wang, B.
Lee, Venus W. Y.
Chan, Mark K. H.
Lee, Francis A. S.
author_facet Yeung, Cynthia S. Y.
Chiang, C. L.
Wong, Natalie S. M.
Ha, S. K.
Tsang, K. S.
Ho, Connie H. M.
Wang, B.
Lee, Venus W. Y.
Chan, Mark K. H.
Lee, Francis A. S.
author_sort Yeung, Cynthia S. Y.
collection PubMed
description This study aims at evaluating the symptom response, response duration, and toxicity of single dose palliative liver radiotherapy (RT) for symptomatic HCC patients. We reviewed unresectable HCC patients treated with palliative RT in our institution. Eligible patients were unsuitable or refractory to trans-arterial chemoembolization (TACE) and stereotactic body radiotherapy (SBRT), with an index symptom of pain or abdominal discomfort. The primary outcome was the percentage of patients with clinical improvement of index symptom at 1 month. Secondary outcomes were response duration, toxicities, alpha-feto protein (AFP) response, and radiological response. Fifty-two patients were included in the study. The index symptom was pain in 34 patients (65.4%), and abdominal discomfort (34.6%) in 18 patients. At 1 month, 51.9% of patients had improvement of symptoms. Median time to symptom progression was 89 days (range: 12–392 days). Treatment was well tolerated with only 2 patients (3.8%) developing grade 3 GI toxicities. AFP response, radiological response rate, and disease control rate at 3 months were 48.6%, 15.1%, and 54.5% respectively. Half of the patients had improvement of index symptoms after receiving palliative liver RT with median response duration of 3 months. The treatment was well tolerated with minimal toxicities.
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spelling pubmed-69851732020-01-31 Palliative Liver Radiotherapy (RT) for Symptomatic Hepatocellular Carcinoma (HCC) Yeung, Cynthia S. Y. Chiang, C. L. Wong, Natalie S. M. Ha, S. K. Tsang, K. S. Ho, Connie H. M. Wang, B. Lee, Venus W. Y. Chan, Mark K. H. Lee, Francis A. S. Sci Rep Article This study aims at evaluating the symptom response, response duration, and toxicity of single dose palliative liver radiotherapy (RT) for symptomatic HCC patients. We reviewed unresectable HCC patients treated with palliative RT in our institution. Eligible patients were unsuitable or refractory to trans-arterial chemoembolization (TACE) and stereotactic body radiotherapy (SBRT), with an index symptom of pain or abdominal discomfort. The primary outcome was the percentage of patients with clinical improvement of index symptom at 1 month. Secondary outcomes were response duration, toxicities, alpha-feto protein (AFP) response, and radiological response. Fifty-two patients were included in the study. The index symptom was pain in 34 patients (65.4%), and abdominal discomfort (34.6%) in 18 patients. At 1 month, 51.9% of patients had improvement of symptoms. Median time to symptom progression was 89 days (range: 12–392 days). Treatment was well tolerated with only 2 patients (3.8%) developing grade 3 GI toxicities. AFP response, radiological response rate, and disease control rate at 3 months were 48.6%, 15.1%, and 54.5% respectively. Half of the patients had improvement of index symptoms after receiving palliative liver RT with median response duration of 3 months. The treatment was well tolerated with minimal toxicities. Nature Publishing Group UK 2020-01-27 /pmc/articles/PMC6985173/ /pubmed/31988376 http://dx.doi.org/10.1038/s41598-020-58108-1 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Yeung, Cynthia S. Y.
Chiang, C. L.
Wong, Natalie S. M.
Ha, S. K.
Tsang, K. S.
Ho, Connie H. M.
Wang, B.
Lee, Venus W. Y.
Chan, Mark K. H.
Lee, Francis A. S.
Palliative Liver Radiotherapy (RT) for Symptomatic Hepatocellular Carcinoma (HCC)
title Palliative Liver Radiotherapy (RT) for Symptomatic Hepatocellular Carcinoma (HCC)
title_full Palliative Liver Radiotherapy (RT) for Symptomatic Hepatocellular Carcinoma (HCC)
title_fullStr Palliative Liver Radiotherapy (RT) for Symptomatic Hepatocellular Carcinoma (HCC)
title_full_unstemmed Palliative Liver Radiotherapy (RT) for Symptomatic Hepatocellular Carcinoma (HCC)
title_short Palliative Liver Radiotherapy (RT) for Symptomatic Hepatocellular Carcinoma (HCC)
title_sort palliative liver radiotherapy (rt) for symptomatic hepatocellular carcinoma (hcc)
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6985173/
https://www.ncbi.nlm.nih.gov/pubmed/31988376
http://dx.doi.org/10.1038/s41598-020-58108-1
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