Cargando…

Partial Virological Response after 2 Years of Entecavir Therapy Increases the Risk of Hepatocellular Carcinoma in Patients with Hepatitis B Virus-Associated Cirrhosis

BACKGROUND/AIMS: The clinical significance of partial virological response (PVR) in patients undergoing antiviral therapy is not well known. This study investigated whether PVR after 2 years of entecavir (ETV) therapy is associated with hepatocellular carcinoma (HCC) development in cirrhotic patient...

Descripción completa

Detalles Bibliográficos
Autores principales: Shin, Seung Kak, Yim, Hyung Joon, Kim, Jeong Han, Lee, Chan Uk, Yeon, Jong Eun, Suh, Sang Jun, Jung, Young Kul, Kim, Yun Soo, Kim, Ju Hyun, Kwon, Oh Sang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Editorial Office of Gut and Liver 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8129658/
https://www.ncbi.nlm.nih.gov/pubmed/33115966
http://dx.doi.org/10.5009/gnl20074
_version_ 1783694344323072000
author Shin, Seung Kak
Yim, Hyung Joon
Kim, Jeong Han
Lee, Chan Uk
Yeon, Jong Eun
Suh, Sang Jun
Jung, Young Kul
Kim, Yun Soo
Kim, Ju Hyun
Kwon, Oh Sang
author_facet Shin, Seung Kak
Yim, Hyung Joon
Kim, Jeong Han
Lee, Chan Uk
Yeon, Jong Eun
Suh, Sang Jun
Jung, Young Kul
Kim, Yun Soo
Kim, Ju Hyun
Kwon, Oh Sang
author_sort Shin, Seung Kak
collection PubMed
description BACKGROUND/AIMS: The clinical significance of partial virological response (PVR) in patients undergoing antiviral therapy is not well known. This study investigated whether PVR after 2 years of entecavir (ETV) therapy is associated with hepatocellular carcinoma (HCC) development in cirrhotic patients. METHODS: A total of 472 naïve patients with hepatitis B virus (HBV)-associated cirrhosis who were treated with ETV for at least 2 years were retrospectively enrolled. Clinical characteristics, laboratory data, PVR, and noninvasive fibrosis markers (aspartate aminotransferase to platelet ratio and FIB-4 index) at 2 years after ETV commencement were analyzed for HCC risk. RESULTS: After excluding those who developed HCC within 2 years of ETV therapy, 359 patients (mean age, 51±10 years; male 64.3%) were examined. During a median follow-up of 82 months, 80 patients developed HCC. In the univariate analysis, older age (hazard ratio [HR], 1.056; p<0.001), PVR (HR, 2.536; p=0.002), higher aspartate aminotransferase (HR, 1.018; p=0.005), lower albumin level (HR, 0.463; p<0.001), lower platelet count (HR, 0.993; p=0.01), and higher FIB-4 index (HR, 1.141; p<0.001) at 2 years after ETV commencement were risk factors for HCC. In the multivariate analysis, older age (HR, 1.046; 95% confidence interval [CI], 1.022 to 1.072; p<0.001), PVR (HR, 2.358; 95% CI, 1.310 to 4.245; p=0.004), and higher FIB-4 index (HR, 1.103; 95% CI, 1.035 to 1.177; p=0.003) were independent risk factors. CONCLUSIONS: PVR and higher FIB-4 index after 2 years of ETV therapy were independent risk factors for HCC. Therefore, efforts to accomplish a complete virological response and reduce the FIB-4 index should be made. (Gut Liver 2021;15-439)
format Online
Article
Text
id pubmed-8129658
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Editorial Office of Gut and Liver
record_format MEDLINE/PubMed
spelling pubmed-81296582021-05-24 Partial Virological Response after 2 Years of Entecavir Therapy Increases the Risk of Hepatocellular Carcinoma in Patients with Hepatitis B Virus-Associated Cirrhosis Shin, Seung Kak Yim, Hyung Joon Kim, Jeong Han Lee, Chan Uk Yeon, Jong Eun Suh, Sang Jun Jung, Young Kul Kim, Yun Soo Kim, Ju Hyun Kwon, Oh Sang Gut Liver Original Article BACKGROUND/AIMS: The clinical significance of partial virological response (PVR) in patients undergoing antiviral therapy is not well known. This study investigated whether PVR after 2 years of entecavir (ETV) therapy is associated with hepatocellular carcinoma (HCC) development in cirrhotic patients. METHODS: A total of 472 naïve patients with hepatitis B virus (HBV)-associated cirrhosis who were treated with ETV for at least 2 years were retrospectively enrolled. Clinical characteristics, laboratory data, PVR, and noninvasive fibrosis markers (aspartate aminotransferase to platelet ratio and FIB-4 index) at 2 years after ETV commencement were analyzed for HCC risk. RESULTS: After excluding those who developed HCC within 2 years of ETV therapy, 359 patients (mean age, 51±10 years; male 64.3%) were examined. During a median follow-up of 82 months, 80 patients developed HCC. In the univariate analysis, older age (hazard ratio [HR], 1.056; p<0.001), PVR (HR, 2.536; p=0.002), higher aspartate aminotransferase (HR, 1.018; p=0.005), lower albumin level (HR, 0.463; p<0.001), lower platelet count (HR, 0.993; p=0.01), and higher FIB-4 index (HR, 1.141; p<0.001) at 2 years after ETV commencement were risk factors for HCC. In the multivariate analysis, older age (HR, 1.046; 95% confidence interval [CI], 1.022 to 1.072; p<0.001), PVR (HR, 2.358; 95% CI, 1.310 to 4.245; p=0.004), and higher FIB-4 index (HR, 1.103; 95% CI, 1.035 to 1.177; p=0.003) were independent risk factors. CONCLUSIONS: PVR and higher FIB-4 index after 2 years of ETV therapy were independent risk factors for HCC. Therefore, efforts to accomplish a complete virological response and reduce the FIB-4 index should be made. (Gut Liver 2021;15-439) Editorial Office of Gut and Liver 2021-05-15 2020-11-02 /pmc/articles/PMC8129658/ /pubmed/33115966 http://dx.doi.org/10.5009/gnl20074 Text en Copyright © Gut and Liver. https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0 (https://creativecommons.org/licenses/by-nc/4.0/) ) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Shin, Seung Kak
Yim, Hyung Joon
Kim, Jeong Han
Lee, Chan Uk
Yeon, Jong Eun
Suh, Sang Jun
Jung, Young Kul
Kim, Yun Soo
Kim, Ju Hyun
Kwon, Oh Sang
Partial Virological Response after 2 Years of Entecavir Therapy Increases the Risk of Hepatocellular Carcinoma in Patients with Hepatitis B Virus-Associated Cirrhosis
title Partial Virological Response after 2 Years of Entecavir Therapy Increases the Risk of Hepatocellular Carcinoma in Patients with Hepatitis B Virus-Associated Cirrhosis
title_full Partial Virological Response after 2 Years of Entecavir Therapy Increases the Risk of Hepatocellular Carcinoma in Patients with Hepatitis B Virus-Associated Cirrhosis
title_fullStr Partial Virological Response after 2 Years of Entecavir Therapy Increases the Risk of Hepatocellular Carcinoma in Patients with Hepatitis B Virus-Associated Cirrhosis
title_full_unstemmed Partial Virological Response after 2 Years of Entecavir Therapy Increases the Risk of Hepatocellular Carcinoma in Patients with Hepatitis B Virus-Associated Cirrhosis
title_short Partial Virological Response after 2 Years of Entecavir Therapy Increases the Risk of Hepatocellular Carcinoma in Patients with Hepatitis B Virus-Associated Cirrhosis
title_sort partial virological response after 2 years of entecavir therapy increases the risk of hepatocellular carcinoma in patients with hepatitis b virus-associated cirrhosis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8129658/
https://www.ncbi.nlm.nih.gov/pubmed/33115966
http://dx.doi.org/10.5009/gnl20074
work_keys_str_mv AT shinseungkak partialvirologicalresponseafter2yearsofentecavirtherapyincreasestheriskofhepatocellularcarcinomainpatientswithhepatitisbvirusassociatedcirrhosis
AT yimhyungjoon partialvirologicalresponseafter2yearsofentecavirtherapyincreasestheriskofhepatocellularcarcinomainpatientswithhepatitisbvirusassociatedcirrhosis
AT kimjeonghan partialvirologicalresponseafter2yearsofentecavirtherapyincreasestheriskofhepatocellularcarcinomainpatientswithhepatitisbvirusassociatedcirrhosis
AT leechanuk partialvirologicalresponseafter2yearsofentecavirtherapyincreasestheriskofhepatocellularcarcinomainpatientswithhepatitisbvirusassociatedcirrhosis
AT yeonjongeun partialvirologicalresponseafter2yearsofentecavirtherapyincreasestheriskofhepatocellularcarcinomainpatientswithhepatitisbvirusassociatedcirrhosis
AT suhsangjun partialvirologicalresponseafter2yearsofentecavirtherapyincreasestheriskofhepatocellularcarcinomainpatientswithhepatitisbvirusassociatedcirrhosis
AT jungyoungkul partialvirologicalresponseafter2yearsofentecavirtherapyincreasestheriskofhepatocellularcarcinomainpatientswithhepatitisbvirusassociatedcirrhosis
AT kimyunsoo partialvirologicalresponseafter2yearsofentecavirtherapyincreasestheriskofhepatocellularcarcinomainpatientswithhepatitisbvirusassociatedcirrhosis
AT kimjuhyun partialvirologicalresponseafter2yearsofentecavirtherapyincreasestheriskofhepatocellularcarcinomainpatientswithhepatitisbvirusassociatedcirrhosis
AT kwonohsang partialvirologicalresponseafter2yearsofentecavirtherapyincreasestheriskofhepatocellularcarcinomainpatientswithhepatitisbvirusassociatedcirrhosis