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Disease Progression in Chronic Hepatitis B Patients under Long-Term Antiviral Therapy
BACKGROUND/AIMS: We investigated factors associated with the disease progression and development of hepatocellular carcinoma (HCC) in chronic hepatitis B (CHB) patients during long-term oral nucleos(t)ide analog (NA) therapy. METHODS: This retrospective study included 524 naive CHB patients who rece...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Gut and Liver
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4413974/ https://www.ncbi.nlm.nih.gov/pubmed/25473072 http://dx.doi.org/10.5009/gnl14170 |
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author | Moon, Jin Chang Kim, Seong Hun Kim, In Hee Lee, Chang Hun Kim, Sang Wook Lee, Seung Ok Lee, Soo Teik Kim, Dae-Ghon |
author_facet | Moon, Jin Chang Kim, Seong Hun Kim, In Hee Lee, Chang Hun Kim, Sang Wook Lee, Seung Ok Lee, Soo Teik Kim, Dae-Ghon |
author_sort | Moon, Jin Chang |
collection | PubMed |
description | BACKGROUND/AIMS: We investigated factors associated with the disease progression and development of hepatocellular carcinoma (HCC) in chronic hepatitis B (CHB) patients during long-term oral nucleos(t)ide analog (NA) therapy. METHODS: This retrospective study included 524 naive CHB patients who received oral NA therapy for more than 48 weeks between January 2003 and December 2007. The primary outcome was 5-year cumulative probability of disease progression and HCC development. Disease progression was defined as cirrhosis development, cirrhotic complications, HCC or liver-related mortality. RESULTS: For the 524 patients, the cumulative probabilities of disease progression and HCC development at 1, 2, 3, 4 and 5 years were 1.1%, 6.3%, 9.0%, 11.6%, and 16.2% and 0.2%, 1.8%, 3.6%, 5.8%, and 9.3%, respectively. In multivariate analysis, age >50 years (hazard ratio [HR], 1.05) and cirrhosis (HR, 2.95) were significant factors for disease progression. Similarly, age >50 years (HR, 1.05), family history of HCC (HR, 5.48), and cirrhosis (HR, 17.16) were significant factors for HCC development. Importantly, longer duration (>12 months) of maintained virological response (<20 IU/mL) reduced the risks of disease progression (HR, 0.19) and HCC development (HR, 0.09). CONCLUSIONS: Longer duration of maintained virological response significantly reduces the risk of disease progression or HCC development in CHB patients undergoing long-term oral NA therapy. |
format | Online Article Text |
id | pubmed-4413974 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Gut and Liver |
record_format | MEDLINE/PubMed |
spelling | pubmed-44139742015-05-06 Disease Progression in Chronic Hepatitis B Patients under Long-Term Antiviral Therapy Moon, Jin Chang Kim, Seong Hun Kim, In Hee Lee, Chang Hun Kim, Sang Wook Lee, Seung Ok Lee, Soo Teik Kim, Dae-Ghon Gut Liver Original Article BACKGROUND/AIMS: We investigated factors associated with the disease progression and development of hepatocellular carcinoma (HCC) in chronic hepatitis B (CHB) patients during long-term oral nucleos(t)ide analog (NA) therapy. METHODS: This retrospective study included 524 naive CHB patients who received oral NA therapy for more than 48 weeks between January 2003 and December 2007. The primary outcome was 5-year cumulative probability of disease progression and HCC development. Disease progression was defined as cirrhosis development, cirrhotic complications, HCC or liver-related mortality. RESULTS: For the 524 patients, the cumulative probabilities of disease progression and HCC development at 1, 2, 3, 4 and 5 years were 1.1%, 6.3%, 9.0%, 11.6%, and 16.2% and 0.2%, 1.8%, 3.6%, 5.8%, and 9.3%, respectively. In multivariate analysis, age >50 years (hazard ratio [HR], 1.05) and cirrhosis (HR, 2.95) were significant factors for disease progression. Similarly, age >50 years (HR, 1.05), family history of HCC (HR, 5.48), and cirrhosis (HR, 17.16) were significant factors for HCC development. Importantly, longer duration (>12 months) of maintained virological response (<20 IU/mL) reduced the risks of disease progression (HR, 0.19) and HCC development (HR, 0.09). CONCLUSIONS: Longer duration of maintained virological response significantly reduces the risk of disease progression or HCC development in CHB patients undergoing long-term oral NA therapy. Gut and Liver 2015-05 2014-12-05 /pmc/articles/PMC4413974/ /pubmed/25473072 http://dx.doi.org/10.5009/gnl14170 Text en Copyright © 2015 by The Korean Society of Gastroenterology, the Korean Society of Gastrointestinal Endoscopy, the Korean Society of Neurogastroenterology and Motility, Korean College of Helicobacter and Upper Gastrointestinal Research, Korean Association for the Study of Intestinal Diseases, the Korean Association for the Study of the Liver, Korean Pancreatobiliary Association, and Korean Society of Gastrointestinal Cancer. This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Moon, Jin Chang Kim, Seong Hun Kim, In Hee Lee, Chang Hun Kim, Sang Wook Lee, Seung Ok Lee, Soo Teik Kim, Dae-Ghon Disease Progression in Chronic Hepatitis B Patients under Long-Term Antiviral Therapy |
title | Disease Progression in Chronic Hepatitis B Patients under Long-Term Antiviral Therapy |
title_full | Disease Progression in Chronic Hepatitis B Patients under Long-Term Antiviral Therapy |
title_fullStr | Disease Progression in Chronic Hepatitis B Patients under Long-Term Antiviral Therapy |
title_full_unstemmed | Disease Progression in Chronic Hepatitis B Patients under Long-Term Antiviral Therapy |
title_short | Disease Progression in Chronic Hepatitis B Patients under Long-Term Antiviral Therapy |
title_sort | disease progression in chronic hepatitis b patients under long-term antiviral therapy |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4413974/ https://www.ncbi.nlm.nih.gov/pubmed/25473072 http://dx.doi.org/10.5009/gnl14170 |
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