The impact of HCV eradication by direct‐acting antivirals on the transition of precancerous hepatic nodules to HCC: A prospective observational study

Background & Aims It remains controversial whether the eradication of hepatitis C virus (HCV) by interferon (IFN)‐free anti‐HCV therapy using direct‐acting antivirals (DAAs) suppresses or promotes hepatocellular carcinoma (HCC) development. We investigated the influence of HCV eradication by DAA...

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Veröffentlicht in:Liver international 2019-03, Vol.39 (3), p.448-454
Hauptverfasser: Toyoda, Hidenori, Kumada, Takashi, Tada, Toshifumi, Mizuno, Kazuyuki, Sone, Yasuhiro, Akita, Tomoyuki, Tanaka, Junko, Johnson, Philip J.
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container_end_page 454
container_issue 3
container_start_page 448
container_title Liver international
container_volume 39
creator Toyoda, Hidenori
Kumada, Takashi
Tada, Toshifumi
Mizuno, Kazuyuki
Sone, Yasuhiro
Akita, Tomoyuki
Tanaka, Junko
Johnson, Philip J.
description Background & Aims It remains controversial whether the eradication of hepatitis C virus (HCV) by interferon (IFN)‐free anti‐HCV therapy using direct‐acting antivirals (DAAs) suppresses or promotes hepatocellular carcinoma (HCC) development. We investigated the influence of HCV eradication by DAA therapy on HCC development, by observing changes of non‐hypervascular hypointense nodules (NHHNs) by gadolinium‐ethoxybenzyl‐diethylenetriamine pentaacetic acid‐enhanced magnetic resonance imaging (EOB‐MRI). Methods A total of 401 patients treated with DAA therapy who did not have a history of HCC were enrolled in this prospective cohort study. All patients underwent EOB‐MRI prior to the start of DAA therapy and were followed up periodically after therapy. The progression of NHHNs detected at baseline to typical HCC, as indicated by hypervascularization and the incidence of newly emergent NHHNs, was analyzed. Results In comparison of patients who achieved sustained virologic response (SVR) with propensity score‐matched patients with persistent HCV infection, there was no difference in the incidence of hypervascularization of NHHNs to typical HCC among patients who had NHHNs at baseline. Among patients who did not have NHHNs at baseline, the incidence of the new emergence of NHHNs did not differ between study patients and propensity score–matched patients with persistent HCV infection. Conclusions During a 2‐year observation period after SVR, the eradication of HCV by IFN‐free DAA therapy did not suppress or enhance HCC development. (UMIN000017020). See Editorial on Page 446
doi_str_mv 10.1111/liv.13987
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We investigated the influence of HCV eradication by DAA therapy on HCC development, by observing changes of non‐hypervascular hypointense nodules (NHHNs) by gadolinium‐ethoxybenzyl‐diethylenetriamine pentaacetic acid‐enhanced magnetic resonance imaging (EOB‐MRI). Methods A total of 401 patients treated with DAA therapy who did not have a history of HCC were enrolled in this prospective cohort study. All patients underwent EOB‐MRI prior to the start of DAA therapy and were followed up periodically after therapy. The progression of NHHNs detected at baseline to typical HCC, as indicated by hypervascularization and the incidence of newly emergent NHHNs, was analyzed. Results In comparison of patients who achieved sustained virologic response (SVR) with propensity score‐matched patients with persistent HCV infection, there was no difference in the incidence of hypervascularization of NHHNs to typical HCC among patients who had NHHNs at baseline. Among patients who did not have NHHNs at baseline, the incidence of the new emergence of NHHNs did not differ between study patients and propensity score–matched patients with persistent HCV infection. Conclusions During a 2‐year observation period after SVR, the eradication of HCV by IFN‐free DAA therapy did not suppress or enhance HCC development. (UMIN000017020). 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We investigated the influence of HCV eradication by DAA therapy on HCC development, by observing changes of non‐hypervascular hypointense nodules (NHHNs) by gadolinium‐ethoxybenzyl‐diethylenetriamine pentaacetic acid‐enhanced magnetic resonance imaging (EOB‐MRI). Methods A total of 401 patients treated with DAA therapy who did not have a history of HCC were enrolled in this prospective cohort study. All patients underwent EOB‐MRI prior to the start of DAA therapy and were followed up periodically after therapy. The progression of NHHNs detected at baseline to typical HCC, as indicated by hypervascularization and the incidence of newly emergent NHHNs, was analyzed. Results In comparison of patients who achieved sustained virologic response (SVR) with propensity score‐matched patients with persistent HCV infection, there was no difference in the incidence of hypervascularization of NHHNs to typical HCC among patients who had NHHNs at baseline. Among patients who did not have NHHNs at baseline, the incidence of the new emergence of NHHNs did not differ between study patients and propensity score–matched patients with persistent HCV infection. Conclusions During a 2‐year observation period after SVR, the eradication of HCV by IFN‐free DAA therapy did not suppress or enhance HCC development. (UMIN000017020). 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dosage</topic><topic>Hepatitis</topic><topic>Hepatitis C</topic><topic>hepatitis C virus</topic><topic>Hepatitis C, Chronic - diagnosis</topic><topic>Hepatitis C, Chronic - drug therapy</topic><topic>Hepatitis C, Chronic - epidemiology</topic><topic>Hepatitis C, Chronic - virology</topic><topic>Hepatocellular carcinoma</topic><topic>Humans</topic><topic>Incidence</topic><topic>Interferon</topic><topic>Liver - diagnostic imaging</topic><topic>Liver - drug effects</topic><topic>Liver - virology</topic><topic>Liver Neoplasms - diagnosis</topic><topic>Liver Neoplasms - epidemiology</topic><topic>Liver Neoplasms - virology</topic><topic>Magnetic Resonance Imaging</topic><topic>Male</topic><topic>Middle Aged</topic><topic>NMR</topic><topic>Nodules</topic><topic>non‐hypervascular hypointense nodules</topic><topic>Nuclear magnetic resonance</topic><topic>Observational studies</topic><topic>Patients</topic><topic>Persistent infection</topic><topic>Precancerous Conditions - diagnostic imaging</topic><topic>Precancerous Conditions - drug therapy</topic><topic>Precancerous Conditions - epidemiology</topic><topic>Precancerous Conditions - virology</topic><topic>Prospective Studies</topic><topic>Risk Factors</topic><topic>Sustained Virologic Response</topic><topic>Therapy</topic><topic>Time Factors</topic><topic>Treatment Outcome</topic><topic>Viruses</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Toyoda, Hidenori</creatorcontrib><creatorcontrib>Kumada, Takashi</creatorcontrib><creatorcontrib>Tada, Toshifumi</creatorcontrib><creatorcontrib>Mizuno, Kazuyuki</creatorcontrib><creatorcontrib>Sone, Yasuhiro</creatorcontrib><creatorcontrib>Akita, Tomoyuki</creatorcontrib><creatorcontrib>Tanaka, Junko</creatorcontrib><creatorcontrib>Johnson, Philip J.</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>Toyoda, Hidenori</au><au>Kumada, Takashi</au><au>Tada, Toshifumi</au><au>Mizuno, Kazuyuki</au><au>Sone, Yasuhiro</au><au>Akita, Tomoyuki</au><au>Tanaka, Junko</au><au>Johnson, Philip J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The impact of HCV eradication by direct‐acting antivirals on the transition of precancerous hepatic nodules to HCC: A prospective observational study</atitle><jtitle>Liver international</jtitle><addtitle>Liver Int</addtitle><date>2019-03</date><risdate>2019</risdate><volume>39</volume><issue>3</issue><spage>448</spage><epage>454</epage><pages>448-454</pages><issn>1478-3223</issn><eissn>1478-3231</eissn><abstract>Background &amp; Aims It remains controversial whether the eradication of hepatitis C virus (HCV) by interferon (IFN)‐free anti‐HCV therapy using direct‐acting antivirals (DAAs) suppresses or promotes hepatocellular carcinoma (HCC) development. We investigated the influence of HCV eradication by DAA therapy on HCC development, by observing changes of non‐hypervascular hypointense nodules (NHHNs) by gadolinium‐ethoxybenzyl‐diethylenetriamine pentaacetic acid‐enhanced magnetic resonance imaging (EOB‐MRI). Methods A total of 401 patients treated with DAA therapy who did not have a history of HCC were enrolled in this prospective cohort study. All patients underwent EOB‐MRI prior to the start of DAA therapy and were followed up periodically after therapy. The progression of NHHNs detected at baseline to typical HCC, as indicated by hypervascularization and the incidence of newly emergent NHHNs, was analyzed. Results In comparison of patients who achieved sustained virologic response (SVR) with propensity score‐matched patients with persistent HCV infection, there was no difference in the incidence of hypervascularization of NHHNs to typical HCC among patients who had NHHNs at baseline. Among patients who did not have NHHNs at baseline, the incidence of the new emergence of NHHNs did not differ between study patients and propensity score–matched patients with persistent HCV infection. Conclusions During a 2‐year observation period after SVR, the eradication of HCV by IFN‐free DAA therapy did not suppress or enhance HCC development. (UMIN000017020). See Editorial on Page 446</abstract><cop>United States</cop><pub>Wiley Subscription Services, Inc</pub><pmid>30312003</pmid><doi>10.1111/liv.13987</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0002-0976-6761</orcidid><orcidid>https://orcid.org/0000-0002-1652-6168</orcidid></addata></record>
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subjects Aged
Aged, 80 and over
Antiviral agents
Antiviral Agents - adverse effects
Antiviral Agents - therapeutic use
Carcinoma, Hepatocellular - diagnosis
Carcinoma, Hepatocellular - epidemiology
Carcinoma, Hepatocellular - virology
Case-Control Studies
Cell Transformation, Viral
Contrast Media - administration & dosage
Diethylenetriamine pentaacetic acid
direct‐acting antiviral therapy
Female
Gadolinium
Gadolinium DTPA - administration & dosage
Hepatitis
Hepatitis C
hepatitis C virus
Hepatitis C, Chronic - diagnosis
Hepatitis C, Chronic - drug therapy
Hepatitis C, Chronic - epidemiology
Hepatitis C, Chronic - virology
Hepatocellular carcinoma
Humans
Incidence
Interferon
Liver - diagnostic imaging
Liver - drug effects
Liver - virology
Liver Neoplasms - diagnosis
Liver Neoplasms - epidemiology
Liver Neoplasms - virology
Magnetic Resonance Imaging
Male
Middle Aged
NMR
Nodules
non‐hypervascular hypointense nodules
Nuclear magnetic resonance
Observational studies
Patients
Persistent infection
Precancerous Conditions - diagnostic imaging
Precancerous Conditions - drug therapy
Precancerous Conditions - epidemiology
Precancerous Conditions - virology
Prospective Studies
Risk Factors
Sustained Virologic Response
Therapy
Time Factors
Treatment Outcome
Viruses
title The impact of HCV eradication by direct‐acting antivirals on the transition of precancerous hepatic nodules to HCC: A prospective observational study
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