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Risk of Hepatocellular Carcinoma Remains High in Patients with HBV-Related Decompensated Cirrhosis and Long-Term Antiviral Therapy

BACKGROUND: This study aimed to evaluate the risk factors of HCC development in patients with hepatitis B virus (HBV)-related DC and who underwent long-term antiviral therapy. METHODS: Data from 308 patients with HBV-related DC and long-term antiviral therapy were collected and retrospectively revie...

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Autores principales: Zhu, Dong-Mei, Xie, Jing, Ye, Chun-Yan, Qian, Mei-Yun, Xue, Yuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7762653/
https://www.ncbi.nlm.nih.gov/pubmed/33381476
http://dx.doi.org/10.1155/2020/8871024
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author Zhu, Dong-Mei
Xie, Jing
Ye, Chun-Yan
Qian, Mei-Yun
Xue, Yuan
author_facet Zhu, Dong-Mei
Xie, Jing
Ye, Chun-Yan
Qian, Mei-Yun
Xue, Yuan
author_sort Zhu, Dong-Mei
collection PubMed
description BACKGROUND: This study aimed to evaluate the risk factors of HCC development in patients with hepatitis B virus (HBV)-related DC and who underwent long-term antiviral therapy. METHODS: Data from 308 patients with HBV-related DC and long-term antiviral therapy were collected and retrospectively reviewed. Cox regression analysis was used to analyze independent risk factors of HCC development. RESULTS: Data from 129 patients with definite records were analyzed. The median follow-up time was 5 years (range, 1 to 8 years). At the end of the follow-up, 41 (31.8%) patients developed HCC, and the time from DC diagnosis to HCC incidence who received antiviral therapy was 4.4 years (range, 1–7 years). The incidence of HCC was higher in males (30/78, 38.5%) than in females (11/51, 21.6%) (P = 0.04). Patients who developed HCC were significantly older than those who did not develop HCC (P < 0.01). The incidence of HCC in patients receiving nucleoside analogues, nucleotide analogues, and combination therapy was 34.7%, 38.1%, and 33.3%, respectively, and the difference showed no significant differences (P = 0.95). Multivariate Cox regression analysis demonstrated that male gender and age ≥50 years are independent risk factors of HCC development (OR = 2.987 and 2.408; 95% CI (1.301–6.858) and (1.126–5.149); P = 0.01 and 0.02, respectively). CONCLUSION: The risk of HCC remains to be high in patients with HBV-related DC, especially in males aged ≥50 years.
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spelling pubmed-77626532020-12-29 Risk of Hepatocellular Carcinoma Remains High in Patients with HBV-Related Decompensated Cirrhosis and Long-Term Antiviral Therapy Zhu, Dong-Mei Xie, Jing Ye, Chun-Yan Qian, Mei-Yun Xue, Yuan Can J Gastroenterol Hepatol Research Article BACKGROUND: This study aimed to evaluate the risk factors of HCC development in patients with hepatitis B virus (HBV)-related DC and who underwent long-term antiviral therapy. METHODS: Data from 308 patients with HBV-related DC and long-term antiviral therapy were collected and retrospectively reviewed. Cox regression analysis was used to analyze independent risk factors of HCC development. RESULTS: Data from 129 patients with definite records were analyzed. The median follow-up time was 5 years (range, 1 to 8 years). At the end of the follow-up, 41 (31.8%) patients developed HCC, and the time from DC diagnosis to HCC incidence who received antiviral therapy was 4.4 years (range, 1–7 years). The incidence of HCC was higher in males (30/78, 38.5%) than in females (11/51, 21.6%) (P = 0.04). Patients who developed HCC were significantly older than those who did not develop HCC (P < 0.01). The incidence of HCC in patients receiving nucleoside analogues, nucleotide analogues, and combination therapy was 34.7%, 38.1%, and 33.3%, respectively, and the difference showed no significant differences (P = 0.95). Multivariate Cox regression analysis demonstrated that male gender and age ≥50 years are independent risk factors of HCC development (OR = 2.987 and 2.408; 95% CI (1.301–6.858) and (1.126–5.149); P = 0.01 and 0.02, respectively). CONCLUSION: The risk of HCC remains to be high in patients with HBV-related DC, especially in males aged ≥50 years. Hindawi 2020-12-17 /pmc/articles/PMC7762653/ /pubmed/33381476 http://dx.doi.org/10.1155/2020/8871024 Text en Copyright © 2020 Dong-Mei Zhu et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Zhu, Dong-Mei
Xie, Jing
Ye, Chun-Yan
Qian, Mei-Yun
Xue, Yuan
Risk of Hepatocellular Carcinoma Remains High in Patients with HBV-Related Decompensated Cirrhosis and Long-Term Antiviral Therapy
title Risk of Hepatocellular Carcinoma Remains High in Patients with HBV-Related Decompensated Cirrhosis and Long-Term Antiviral Therapy
title_full Risk of Hepatocellular Carcinoma Remains High in Patients with HBV-Related Decompensated Cirrhosis and Long-Term Antiviral Therapy
title_fullStr Risk of Hepatocellular Carcinoma Remains High in Patients with HBV-Related Decompensated Cirrhosis and Long-Term Antiviral Therapy
title_full_unstemmed Risk of Hepatocellular Carcinoma Remains High in Patients with HBV-Related Decompensated Cirrhosis and Long-Term Antiviral Therapy
title_short Risk of Hepatocellular Carcinoma Remains High in Patients with HBV-Related Decompensated Cirrhosis and Long-Term Antiviral Therapy
title_sort risk of hepatocellular carcinoma remains high in patients with hbv-related decompensated cirrhosis and long-term antiviral therapy
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7762653/
https://www.ncbi.nlm.nih.gov/pubmed/33381476
http://dx.doi.org/10.1155/2020/8871024
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