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Tenofovir disoproxil fumarate reduce incidence of HCC development in CHB-patients with compensated cirrhosis
BACKGROUND: The impact of different anti-virus regimens on prognosis of Chronic hepatitis B (CHB) related cirrhosis remains to be explored. We aim to investigate whether CHB-related HCC patients receiving nucleoside analogue regimen or not have a different prognosis. METHODS: Two hundred forty-two C...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6114711/ https://www.ncbi.nlm.nih.gov/pubmed/30181772 http://dx.doi.org/10.1186/s13027-018-0203-8 |
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author | Zhang, Ping Liu, Qingli Yuan, Mei Wang, Lina |
author_facet | Zhang, Ping Liu, Qingli Yuan, Mei Wang, Lina |
author_sort | Zhang, Ping |
collection | PubMed |
description | BACKGROUND: The impact of different anti-virus regimens on prognosis of Chronic hepatitis B (CHB) related cirrhosis remains to be explored. We aim to investigate whether CHB-related HCC patients receiving nucleoside analogue regimen or not have a different prognosis. METHODS: Two hundred forty-two CHB-related compensated cirrhosis patients were attributed into groups regarding their anti-virus regimens containing tenofovir disoproxil fumarate (TDF) or not. The results of two groups were reviewed and investigated. The probability of hepatocellular carcinoma (HCC) development among each group were analyzed and compared. RESULTS: Two hundred forty-two CHB-related compensated cirrhosis patients from 2008 June to 2011 December were included in our study. One hundred twenty-seven patients received anti-virus regimen containing TDF and 115 patients received anti-virus regimen without TDF. Child-Pugh score, alanine aminotransferase (ALT), total bilirubin level, status of hepatitis B e antigen (HBeAg) and serum HBV DNA level were compared between groups. The cumulative probability of HCC development in TDF-contained group were significantly lower than it in non-TDF-contained group (p < 0.05). Multi-variant analysis indicated that TDF-containing regimen treatment was significantly associated with lower probability of HCC development, (hazard ratio, 0.18; 95% confidence interval range, 0.07–0.45, p < 0.05). CONCLUSION: Anti-virus regimen containing TDF benefits for the prognosis of CHB-related liver cirrhosis patients. |
format | Online Article Text |
id | pubmed-6114711 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-61147112018-09-04 Tenofovir disoproxil fumarate reduce incidence of HCC development in CHB-patients with compensated cirrhosis Zhang, Ping Liu, Qingli Yuan, Mei Wang, Lina Infect Agent Cancer Research Article BACKGROUND: The impact of different anti-virus regimens on prognosis of Chronic hepatitis B (CHB) related cirrhosis remains to be explored. We aim to investigate whether CHB-related HCC patients receiving nucleoside analogue regimen or not have a different prognosis. METHODS: Two hundred forty-two CHB-related compensated cirrhosis patients were attributed into groups regarding their anti-virus regimens containing tenofovir disoproxil fumarate (TDF) or not. The results of two groups were reviewed and investigated. The probability of hepatocellular carcinoma (HCC) development among each group were analyzed and compared. RESULTS: Two hundred forty-two CHB-related compensated cirrhosis patients from 2008 June to 2011 December were included in our study. One hundred twenty-seven patients received anti-virus regimen containing TDF and 115 patients received anti-virus regimen without TDF. Child-Pugh score, alanine aminotransferase (ALT), total bilirubin level, status of hepatitis B e antigen (HBeAg) and serum HBV DNA level were compared between groups. The cumulative probability of HCC development in TDF-contained group were significantly lower than it in non-TDF-contained group (p < 0.05). Multi-variant analysis indicated that TDF-containing regimen treatment was significantly associated with lower probability of HCC development, (hazard ratio, 0.18; 95% confidence interval range, 0.07–0.45, p < 0.05). CONCLUSION: Anti-virus regimen containing TDF benefits for the prognosis of CHB-related liver cirrhosis patients. BioMed Central 2018-08-29 /pmc/articles/PMC6114711/ /pubmed/30181772 http://dx.doi.org/10.1186/s13027-018-0203-8 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Zhang, Ping Liu, Qingli Yuan, Mei Wang, Lina Tenofovir disoproxil fumarate reduce incidence of HCC development in CHB-patients with compensated cirrhosis |
title | Tenofovir disoproxil fumarate reduce incidence of HCC development in CHB-patients with compensated cirrhosis |
title_full | Tenofovir disoproxil fumarate reduce incidence of HCC development in CHB-patients with compensated cirrhosis |
title_fullStr | Tenofovir disoproxil fumarate reduce incidence of HCC development in CHB-patients with compensated cirrhosis |
title_full_unstemmed | Tenofovir disoproxil fumarate reduce incidence of HCC development in CHB-patients with compensated cirrhosis |
title_short | Tenofovir disoproxil fumarate reduce incidence of HCC development in CHB-patients with compensated cirrhosis |
title_sort | tenofovir disoproxil fumarate reduce incidence of hcc development in chb-patients with compensated cirrhosis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6114711/ https://www.ncbi.nlm.nih.gov/pubmed/30181772 http://dx.doi.org/10.1186/s13027-018-0203-8 |
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