The risk of hepatocellular carcinoma within and beyond the first 5 years of entecavir in Korean patients with chronic hepatitis B

Background & Aims The development of hepatocellular carcinoma (HCC) in patients with chronic hepatitis B (CHB) has decreased due to potent antiviral agents. However, it remains uncertain whether the risk of HCC will diminish after long‐term antiviral therapy in Asia, where CHB is endemic and ver...

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Veröffentlicht in:Liver international 2018-12, Vol.38 (12), p.2269-2276
Hauptverfasser: Kim, Byung Gyu, Park, Neung Hwa, Lee, Seung Bum, Jeon, Soyoung, Park, Jae Ho, Jung, Seok Won, Jeong, In Du, Bang, Sung‐Jo, Shin, Jung Woo
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container_end_page 2276
container_issue 12
container_start_page 2269
container_title Liver international
container_volume 38
creator Kim, Byung Gyu
Park, Neung Hwa
Lee, Seung Bum
Jeon, Soyoung
Park, Jae Ho
Jung, Seok Won
Jeong, In Du
Bang, Sung‐Jo
Shin, Jung Woo
description Background & Aims The development of hepatocellular carcinoma (HCC) in patients with chronic hepatitis B (CHB) has decreased due to potent antiviral agents. However, it remains uncertain whether the risk of HCC will diminish after long‐term antiviral therapy in Asia, where CHB is endemic and vertical transmission is common. This study aimed to compare the incidence of HCC within and beyond the first 5 years of entecavir (ETV) in treatment‐naïve Korean patients with CHB. Methods We performed a retrospective observational analysis of data from 894 consecutive, adult patients with CHB undergoing ETV treatment at a tertiary referral hospital in Ulsan, Korea from January 1, 2007 through April 31, 2017. We compared the HCC incidence rates per 100 person‐years within and beyond the first 5 years. Univariate and multivariate analyses for factors predictive of HCC were performed. Results The incidence rate of HCC in patients with CHB did not differ statistically when we compared within and beyond the first 5 years of ETV therapy (2.29% vs 1.66% per person‐year, P = 0.217). Failure to achieve maintained virological response (MVR) was a major independent risk factor for HCC in patients at a follow‐up of
doi_str_mv 10.1111/liv.13938
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However, it remains uncertain whether the risk of HCC will diminish after long‐term antiviral therapy in Asia, where CHB is endemic and vertical transmission is common. This study aimed to compare the incidence of HCC within and beyond the first 5 years of entecavir (ETV) in treatment‐naïve Korean patients with CHB. Methods We performed a retrospective observational analysis of data from 894 consecutive, adult patients with CHB undergoing ETV treatment at a tertiary referral hospital in Ulsan, Korea from January 1, 2007 through April 31, 2017. We compared the HCC incidence rates per 100 person‐years within and beyond the first 5 years. Univariate and multivariate analyses for factors predictive of HCC were performed. Results The incidence rate of HCC in patients with CHB did not differ statistically when we compared within and beyond the first 5 years of ETV therapy (2.29% vs 1.66% per person‐year, P = 0.217). Failure to achieve maintained virological response (MVR) was a major independent risk factor for HCC in patients at a follow‐up of &lt;5 years. In contrast, in patients with a follow‐up of ≥5 years, achieving MVR was not significantly associated with HCC development. Conclusions The incidence rate of HCC may not change significantly before and after 5 years of ETV therapy in Korean CHB patients. The risk of HCC in Asian CHB patients may remain in the long‐term.</description><identifier>ISSN: 1478-3223</identifier><identifier>EISSN: 1478-3231</identifier><identifier>DOI: 10.1111/liv.13938</identifier><identifier>PMID: 30052303</identifier><language>eng</language><publisher>United States: Wiley Subscription Services, Inc</publisher><subject>Adult ; Antiviral agents ; Antiviral Agents - therapeutic use ; antiviral therapy ; Carcinoma, Hepatocellular - epidemiology ; Carcinoma, Hepatocellular - etiology ; cirrhosis ; Data processing ; Disease transmission ; DNA, Viral - blood ; Female ; Guanine - analogs &amp; derivatives ; Guanine - therapeutic use ; Hepatitis ; Hepatitis B ; hepatitis B virus ; Hepatitis B virus - genetics ; Hepatitis B, Chronic - complications ; Hepatitis B, Chronic - drug therapy ; Hepatocellular carcinoma ; Humans ; Incidence ; Interferon ; Liver cancer ; Liver Cirrhosis - etiology ; Liver Neoplasms - epidemiology ; Liver Neoplasms - etiology ; Longitudinal Studies ; Male ; Middle Aged ; Multivariate Analysis ; Patients ; Performance prediction ; Republic of Korea - epidemiology ; Retrospective Studies ; Risk analysis ; Risk Factors ; Sustained Virologic Response ; Therapy ; Treatment Failure ; Viral Load</subject><ispartof>Liver international, 2018-12, Vol.38 (12), p.2269-2276</ispartof><rights>2018 John Wiley &amp; Sons A/S. Published by John Wiley &amp; Sons Ltd</rights><rights>2018 John Wiley &amp; Sons A/S. 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However, it remains uncertain whether the risk of HCC will diminish after long‐term antiviral therapy in Asia, where CHB is endemic and vertical transmission is common. This study aimed to compare the incidence of HCC within and beyond the first 5 years of entecavir (ETV) in treatment‐naïve Korean patients with CHB. Methods We performed a retrospective observational analysis of data from 894 consecutive, adult patients with CHB undergoing ETV treatment at a tertiary referral hospital in Ulsan, Korea from January 1, 2007 through April 31, 2017. We compared the HCC incidence rates per 100 person‐years within and beyond the first 5 years. Univariate and multivariate analyses for factors predictive of HCC were performed. Results The incidence rate of HCC in patients with CHB did not differ statistically when we compared within and beyond the first 5 years of ETV therapy (2.29% vs 1.66% per person‐year, P = 0.217). Failure to achieve maintained virological response (MVR) was a major independent risk factor for HCC in patients at a follow‐up of &lt;5 years. In contrast, in patients with a follow‐up of ≥5 years, achieving MVR was not significantly associated with HCC development. Conclusions The incidence rate of HCC may not change significantly before and after 5 years of ETV therapy in Korean CHB patients. 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Park, Neung Hwa ; Lee, Seung Bum ; Jeon, Soyoung ; Park, Jae Ho ; Jung, Seok Won ; Jeong, In Du ; Bang, Sung‐Jo ; Shin, Jung Woo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3538-cdb43cf634dd5a93a35248fb67358d6f7518bc7230c521408b429701bc21bcb73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Adult</topic><topic>Antiviral agents</topic><topic>Antiviral Agents - therapeutic use</topic><topic>antiviral therapy</topic><topic>Carcinoma, Hepatocellular - epidemiology</topic><topic>Carcinoma, Hepatocellular - etiology</topic><topic>cirrhosis</topic><topic>Data processing</topic><topic>Disease transmission</topic><topic>DNA, Viral - blood</topic><topic>Female</topic><topic>Guanine - analogs &amp; derivatives</topic><topic>Guanine - therapeutic use</topic><topic>Hepatitis</topic><topic>Hepatitis B</topic><topic>hepatitis B virus</topic><topic>Hepatitis B virus - genetics</topic><topic>Hepatitis B, Chronic - complications</topic><topic>Hepatitis B, Chronic - drug therapy</topic><topic>Hepatocellular carcinoma</topic><topic>Humans</topic><topic>Incidence</topic><topic>Interferon</topic><topic>Liver cancer</topic><topic>Liver Cirrhosis - etiology</topic><topic>Liver Neoplasms - epidemiology</topic><topic>Liver Neoplasms - etiology</topic><topic>Longitudinal Studies</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Multivariate Analysis</topic><topic>Patients</topic><topic>Performance prediction</topic><topic>Republic of Korea - epidemiology</topic><topic>Retrospective Studies</topic><topic>Risk analysis</topic><topic>Risk Factors</topic><topic>Sustained Virologic Response</topic><topic>Therapy</topic><topic>Treatment Failure</topic><topic>Viral Load</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kim, Byung Gyu</creatorcontrib><creatorcontrib>Park, Neung Hwa</creatorcontrib><creatorcontrib>Lee, Seung Bum</creatorcontrib><creatorcontrib>Jeon, Soyoung</creatorcontrib><creatorcontrib>Park, Jae Ho</creatorcontrib><creatorcontrib>Jung, Seok Won</creatorcontrib><creatorcontrib>Jeong, In Du</creatorcontrib><creatorcontrib>Bang, Sung‐Jo</creatorcontrib><creatorcontrib>Shin, Jung Woo</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Immunology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Liver international</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kim, Byung Gyu</au><au>Park, Neung Hwa</au><au>Lee, Seung Bum</au><au>Jeon, Soyoung</au><au>Park, Jae Ho</au><au>Jung, Seok Won</au><au>Jeong, In Du</au><au>Bang, Sung‐Jo</au><au>Shin, Jung Woo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The risk of hepatocellular carcinoma within and beyond the first 5 years of entecavir in Korean patients with chronic hepatitis B</atitle><jtitle>Liver international</jtitle><addtitle>Liver Int</addtitle><date>2018-12</date><risdate>2018</risdate><volume>38</volume><issue>12</issue><spage>2269</spage><epage>2276</epage><pages>2269-2276</pages><issn>1478-3223</issn><eissn>1478-3231</eissn><abstract>Background &amp; Aims The development of hepatocellular carcinoma (HCC) in patients with chronic hepatitis B (CHB) has decreased due to potent antiviral agents. However, it remains uncertain whether the risk of HCC will diminish after long‐term antiviral therapy in Asia, where CHB is endemic and vertical transmission is common. This study aimed to compare the incidence of HCC within and beyond the first 5 years of entecavir (ETV) in treatment‐naïve Korean patients with CHB. Methods We performed a retrospective observational analysis of data from 894 consecutive, adult patients with CHB undergoing ETV treatment at a tertiary referral hospital in Ulsan, Korea from January 1, 2007 through April 31, 2017. We compared the HCC incidence rates per 100 person‐years within and beyond the first 5 years. Univariate and multivariate analyses for factors predictive of HCC were performed. Results The incidence rate of HCC in patients with CHB did not differ statistically when we compared within and beyond the first 5 years of ETV therapy (2.29% vs 1.66% per person‐year, P = 0.217). Failure to achieve maintained virological response (MVR) was a major independent risk factor for HCC in patients at a follow‐up of &lt;5 years. In contrast, in patients with a follow‐up of ≥5 years, achieving MVR was not significantly associated with HCC development. Conclusions The incidence rate of HCC may not change significantly before and after 5 years of ETV therapy in Korean CHB patients. The risk of HCC in Asian CHB patients may remain in the long‐term.</abstract><cop>United States</cop><pub>Wiley Subscription Services, Inc</pub><pmid>30052303</pmid><doi>10.1111/liv.13938</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0002-5880-5659</orcidid></addata></record>
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source MEDLINE; Wiley Online Library Journals Frontfile Complete
subjects Adult
Antiviral agents
Antiviral Agents - therapeutic use
antiviral therapy
Carcinoma, Hepatocellular - epidemiology
Carcinoma, Hepatocellular - etiology
cirrhosis
Data processing
Disease transmission
DNA, Viral - blood
Female
Guanine - analogs & derivatives
Guanine - therapeutic use
Hepatitis
Hepatitis B
hepatitis B virus
Hepatitis B virus - genetics
Hepatitis B, Chronic - complications
Hepatitis B, Chronic - drug therapy
Hepatocellular carcinoma
Humans
Incidence
Interferon
Liver cancer
Liver Cirrhosis - etiology
Liver Neoplasms - epidemiology
Liver Neoplasms - etiology
Longitudinal Studies
Male
Middle Aged
Multivariate Analysis
Patients
Performance prediction
Republic of Korea - epidemiology
Retrospective Studies
Risk analysis
Risk Factors
Sustained Virologic Response
Therapy
Treatment Failure
Viral Load
title The risk of hepatocellular carcinoma within and beyond the first 5 years of entecavir in Korean patients with chronic hepatitis B
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