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Differences in background characteristics of patients with chronic hepatitis C who achieved sustained virologic response with interferon‐free versus interferon‐based therapy and the risk of developing hepatocellular carcinoma after eradication of hepatitis C virus in Japan

Summary We compared the background characteristics of patients with chronic hepatitis C who achieved eradication of hepatitis C virus (HCV), that is sustained virologic response (SVR), with interferon (IFN)‐based versus IFN‐free antiviral therapy in Japan. In addition, we used a previously reported...

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Published in:Journal of viral hepatitis 2017-06, Vol.24 (6), p.472-476
Main Authors: Toyoda, H., Tada, T., Takaguchi, K., Senoh, T., Shimada, N., Hiraoka, A., Michitaka, K., Ishikawa, T., Kumada, T.
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cited_by cdi_FETCH-LOGICAL-c3535-6f78bd5359007b227c885a54fa68b295143e0377363143dc1b3eaaa9e89f6c513
cites cdi_FETCH-LOGICAL-c3535-6f78bd5359007b227c885a54fa68b295143e0377363143dc1b3eaaa9e89f6c513
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container_issue 6
container_start_page 472
container_title Journal of viral hepatitis
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creator Toyoda, H.
Tada, T.
Takaguchi, K.
Senoh, T.
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Kumada, T.
description Summary We compared the background characteristics of patients with chronic hepatitis C who achieved eradication of hepatitis C virus (HCV), that is sustained virologic response (SVR), with interferon (IFN)‐based versus IFN‐free antiviral therapy in Japan. In addition, we used a previously reported risk assessment model to compare the incidence of hepatocellular carcinoma (HCC) after SVR by treatment type. Pretreatment characteristics of 1533 patients who achieved SVR with IFN‐based therapy and 1086 patients with IFN‐free therapy from five institutions across Japan were compared. The risk of HCC after SVR was assessed based on pretreatment characteristics, and the incidence of HCC after SVR was estimated in both groups. Age and serum alpha‐fetoprotein levels were higher, platelet count was lower, and liver fibrosis was more advanced in patients who achieved SVR with IFN‐free therapy compared with IFN‐based therapy. The incidence of HCC after SVR in the IFN‐free group was estimated to be more than twofold higher than in the IFN‐based therapy group (7.29% vs. 3.09%, and 6.23% vs. 3.01% when excluding patients who have underwent curative treatment for HCC). There are large differences in pretreatment characteristics between patients who achieved SVR with IFN‐based and IFN‐free therapies in Japan, which are associated with differential risk of HCC after SVR. These differences can influence the incidence of HCC after SVR and should be taken into consideration when comparing IFN‐based and IFN‐free therapies in terms of hepatocarcinogenesis suppression with HCV eradication.
doi_str_mv 10.1111/jvh.12665
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In addition, we used a previously reported risk assessment model to compare the incidence of hepatocellular carcinoma (HCC) after SVR by treatment type. Pretreatment characteristics of 1533 patients who achieved SVR with IFN‐based therapy and 1086 patients with IFN‐free therapy from five institutions across Japan were compared. The risk of HCC after SVR was assessed based on pretreatment characteristics, and the incidence of HCC after SVR was estimated in both groups. Age and serum alpha‐fetoprotein levels were higher, platelet count was lower, and liver fibrosis was more advanced in patients who achieved SVR with IFN‐free therapy compared with IFN‐based therapy. The incidence of HCC after SVR in the IFN‐free group was estimated to be more than twofold higher than in the IFN‐based therapy group (7.29% vs. 3.09%, and 6.23% vs. 3.01% when excluding patients who have underwent curative treatment for HCC). There are large differences in pretreatment characteristics between patients who achieved SVR with IFN‐based and IFN‐free therapies in Japan, which are associated with differential risk of HCC after SVR. These differences can influence the incidence of HCC after SVR and should be taken into consideration when comparing IFN‐based and IFN‐free therapies in terms of hepatocarcinogenesis suppression with HCV eradication.</description><identifier>ISSN: 1352-0504</identifier><identifier>EISSN: 1365-2893</identifier><identifier>DOI: 10.1111/jvh.12665</identifier><identifier>PMID: 27983762</identifier><language>eng</language><publisher>England: Wiley Subscription Services, Inc</publisher><subject>Adult ; Aged ; Aged, 80 and over ; Antiviral agents ; Antiviral Agents - therapeutic use ; Carcinoma, Hepatocellular - epidemiology ; chronic hepatitis C ; Female ; Fibrosis ; Hepatitis ; Hepatitis C ; Hepatitis C, Chronic - complications ; Hepatitis C, Chronic - drug therapy ; Hepatitis C, Chronic - pathology ; Hepatocellular carcinoma ; Humans ; IFN‐based therapy ; IFN‐free therapy ; Incidence ; Interferon ; Interferons - therapeutic use ; Japan - epidemiology ; Liver cancer ; Liver Neoplasms - epidemiology ; Male ; Middle Aged ; Risk Assessment ; risk score ; Sustained Virologic Response ; α-Fetoprotein</subject><ispartof>Journal of viral hepatitis, 2017-06, Vol.24 (6), p.472-476</ispartof><rights>2017 John Wiley &amp; Sons Ltd</rights><rights>2017 John Wiley &amp; Sons Ltd.</rights><rights>Copyright © 2017 John Wiley &amp; Sons Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3535-6f78bd5359007b227c885a54fa68b295143e0377363143dc1b3eaaa9e89f6c513</citedby><cites>FETCH-LOGICAL-c3535-6f78bd5359007b227c885a54fa68b295143e0377363143dc1b3eaaa9e89f6c513</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27983762$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Toyoda, H.</creatorcontrib><creatorcontrib>Tada, T.</creatorcontrib><creatorcontrib>Takaguchi, K.</creatorcontrib><creatorcontrib>Senoh, T.</creatorcontrib><creatorcontrib>Shimada, N.</creatorcontrib><creatorcontrib>Hiraoka, A.</creatorcontrib><creatorcontrib>Michitaka, K.</creatorcontrib><creatorcontrib>Ishikawa, T.</creatorcontrib><creatorcontrib>Kumada, T.</creatorcontrib><title>Differences in background characteristics of patients with chronic hepatitis C who achieved sustained virologic response with interferon‐free versus interferon‐based therapy and the risk of developing hepatocellular carcinoma after eradication of hepatitis C virus in Japan</title><title>Journal of viral hepatitis</title><addtitle>J Viral Hepat</addtitle><description>Summary We compared the background characteristics of patients with chronic hepatitis C who achieved eradication of hepatitis C virus (HCV), that is sustained virologic response (SVR), with interferon (IFN)‐based versus IFN‐free antiviral therapy in Japan. In addition, we used a previously reported risk assessment model to compare the incidence of hepatocellular carcinoma (HCC) after SVR by treatment type. Pretreatment characteristics of 1533 patients who achieved SVR with IFN‐based therapy and 1086 patients with IFN‐free therapy from five institutions across Japan were compared. The risk of HCC after SVR was assessed based on pretreatment characteristics, and the incidence of HCC after SVR was estimated in both groups. Age and serum alpha‐fetoprotein levels were higher, platelet count was lower, and liver fibrosis was more advanced in patients who achieved SVR with IFN‐free therapy compared with IFN‐based therapy. The incidence of HCC after SVR in the IFN‐free group was estimated to be more than twofold higher than in the IFN‐based therapy group (7.29% vs. 3.09%, and 6.23% vs. 3.01% when excluding patients who have underwent curative treatment for HCC). There are large differences in pretreatment characteristics between patients who achieved SVR with IFN‐based and IFN‐free therapies in Japan, which are associated with differential risk of HCC after SVR. 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In addition, we used a previously reported risk assessment model to compare the incidence of hepatocellular carcinoma (HCC) after SVR by treatment type. Pretreatment characteristics of 1533 patients who achieved SVR with IFN‐based therapy and 1086 patients with IFN‐free therapy from five institutions across Japan were compared. The risk of HCC after SVR was assessed based on pretreatment characteristics, and the incidence of HCC after SVR was estimated in both groups. Age and serum alpha‐fetoprotein levels were higher, platelet count was lower, and liver fibrosis was more advanced in patients who achieved SVR with IFN‐free therapy compared with IFN‐based therapy. The incidence of HCC after SVR in the IFN‐free group was estimated to be more than twofold higher than in the IFN‐based therapy group (7.29% vs. 3.09%, and 6.23% vs. 3.01% when excluding patients who have underwent curative treatment for HCC). There are large differences in pretreatment characteristics between patients who achieved SVR with IFN‐based and IFN‐free therapies in Japan, which are associated with differential risk of HCC after SVR. These differences can influence the incidence of HCC after SVR and should be taken into consideration when comparing IFN‐based and IFN‐free therapies in terms of hepatocarcinogenesis suppression with HCV eradication.</abstract><cop>England</cop><pub>Wiley Subscription Services, Inc</pub><pmid>27983762</pmid><doi>10.1111/jvh.12665</doi><tpages>5</tpages></addata></record>
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source Wiley-Blackwell Read & Publish Collection
subjects Adult
Aged
Aged, 80 and over
Antiviral agents
Antiviral Agents - therapeutic use
Carcinoma, Hepatocellular - epidemiology
chronic hepatitis C
Female
Fibrosis
Hepatitis
Hepatitis C
Hepatitis C, Chronic - complications
Hepatitis C, Chronic - drug therapy
Hepatitis C, Chronic - pathology
Hepatocellular carcinoma
Humans
IFN‐based therapy
IFN‐free therapy
Incidence
Interferon
Interferons - therapeutic use
Japan - epidemiology
Liver cancer
Liver Neoplasms - epidemiology
Male
Middle Aged
Risk Assessment
risk score
Sustained Virologic Response
α-Fetoprotein
title Differences in background characteristics of patients with chronic hepatitis C who achieved sustained virologic response with interferon‐free versus interferon‐based therapy and the risk of developing hepatocellular carcinoma after eradication of hepatitis C virus in Japan
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