All‐cause hepatocellular carcinoma survival in the era of direct‐acting antiviral therapy

Background and Aim Hepatitis C virus (HCV) cure with direct‐acting antiviral (DAA) therapy improves survival in patients with HCV‐related hepatocellular carcinoma (HCC). We hypothesized that HCV‐HCC survival has increased in the DAA era, more than other aetiologies of HCC. We aimed to evaluate survi...

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Veröffentlicht in:Journal of gastroenterology and hepatology 2021-12, Vol.36 (12), p.3515-3523
Hauptverfasser: Lockart, Ian, Hajarizadeh, Behzad, Buckley, Niamh, Davison, Scott, Prakoso, Emilia, Levy, Miriam T, George, Jacob, Dore, Gregory J, Danta, Mark
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container_end_page 3523
container_issue 12
container_start_page 3515
container_title Journal of gastroenterology and hepatology
container_volume 36
creator Lockart, Ian
Hajarizadeh, Behzad
Buckley, Niamh
Davison, Scott
Prakoso, Emilia
Levy, Miriam T
George, Jacob
Dore, Gregory J
Danta, Mark
description Background and Aim Hepatitis C virus (HCV) cure with direct‐acting antiviral (DAA) therapy improves survival in patients with HCV‐related hepatocellular carcinoma (HCC). We hypothesized that HCV‐HCC survival has increased in the DAA era, more than other aetiologies of HCC. We aimed to evaluate survival following HCC diagnosis in the pre‐DAA and DAA eras, across each aetiology of HCC. Methods Patients with HCC at three tertiary referral hospitals were included retrospectively (January 2008 to December 2019). Patients were categorized as HCV‐HCC, hepatitis B virus (HBV)‐HCC, or non‐viral HCC. For each aetiology, the risk of death following incident HCC among patients diagnosed in the DAA era (2015–2019) was compared with patients diagnosed in the pre‐DAA era (2008–2014). Results Among 1161 patients, there were 422 (36%) patients with HCV‐HCC, 227 (20%) with HBV‐HCC, and 512 (44%) with non‐viral HCC. In adjusted analysis, the risk of death was lower in patients with HCV‐HCC diagnosed in 2015–2019, compared with patients diagnosed in 2008–2014 (adjusted hazard ratio [aHR]: 0.68; 95% confidence interval [CI]: 0.52–0.89; P = 0.005). In contrast, there was no difference in the risk of death between time periods for patients with HBV‐HCC (HR: 0.91; 95% CI: 0.64–1.29; P = 0.602) or non‐viral HCC on adjusted analysis (aHR: 0.92; 95% CI: 0.74–1.15; P = 0.476). Although patients with HBV‐HCC had better survival compared with patients with HCV‐HCC in 2008–2014 (aHR: 0.74; 95% CI: 0.55–0.98; P = 0.037), this difference disappeared in 2015–2019 (aHR: 1.26; 95% CI: 0.90–1.77; P = 0.175). Conclusions Hepatitis C virus‐related HCC survival has increased in the DAA era, whereas adjusted survival remained stable for HBV‐HCC and non‐viral HCC.
doi_str_mv 10.1111/jgh.15687
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We hypothesized that HCV‐HCC survival has increased in the DAA era, more than other aetiologies of HCC. We aimed to evaluate survival following HCC diagnosis in the pre‐DAA and DAA eras, across each aetiology of HCC. Methods Patients with HCC at three tertiary referral hospitals were included retrospectively (January 2008 to December 2019). Patients were categorized as HCV‐HCC, hepatitis B virus (HBV)‐HCC, or non‐viral HCC. For each aetiology, the risk of death following incident HCC among patients diagnosed in the DAA era (2015–2019) was compared with patients diagnosed in the pre‐DAA era (2008–2014). Results Among 1161 patients, there were 422 (36%) patients with HCV‐HCC, 227 (20%) with HBV‐HCC, and 512 (44%) with non‐viral HCC. In adjusted analysis, the risk of death was lower in patients with HCV‐HCC diagnosed in 2015–2019, compared with patients diagnosed in 2008–2014 (adjusted hazard ratio [aHR]: 0.68; 95% confidence interval [CI]: 0.52–0.89; P = 0.005). In contrast, there was no difference in the risk of death between time periods for patients with HBV‐HCC (HR: 0.91; 95% CI: 0.64–1.29; P = 0.602) or non‐viral HCC on adjusted analysis (aHR: 0.92; 95% CI: 0.74–1.15; P = 0.476). Although patients with HBV‐HCC had better survival compared with patients with HCV‐HCC in 2008–2014 (aHR: 0.74; 95% CI: 0.55–0.98; P = 0.037), this difference disappeared in 2015–2019 (aHR: 1.26; 95% CI: 0.90–1.77; P = 0.175). Conclusions Hepatitis C virus‐related HCC survival has increased in the DAA era, whereas adjusted survival remained stable for HBV‐HCC and non‐viral HCC.</description><identifier>ISSN: 0815-9319</identifier><identifier>EISSN: 1440-1746</identifier><identifier>DOI: 10.1111/jgh.15687</identifier><identifier>PMID: 34520088</identifier><language>eng</language><publisher>Australia: Wiley Subscription Services, Inc</publisher><subject>Antiviral agents ; Antiviral Agents - therapeutic use ; Carcinoma, Hepatocellular - mortality ; Carcinoma, Hepatocellular - virology ; Death ; Hepatitis B ; Hepatitis C ; Hepatitis C, Chronic - complications ; Hepatitis C, Chronic - drug therapy ; Hepatocellular carcinoma ; Humans ; Liver cancer ; Liver Neoplasms - mortality ; Liver Neoplasms - virology ; Patients ; Retrospective Studies ; Survival ; Survival Analysis ; Viruses</subject><ispartof>Journal of gastroenterology and hepatology, 2021-12, Vol.36 (12), p.3515-3523</ispartof><rights>2021 Journal of Gastroenterology and Hepatology Foundation and John Wiley &amp; Sons Australia, Ltd</rights><rights>2021 Journal of Gastroenterology and Hepatology Foundation and John Wiley &amp; Sons Australia, Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3537-77017cf44e92c18b01e11235ae5dd5a9be9d85de183ba4d936ac86dbb9b009c13</citedby><cites>FETCH-LOGICAL-c3537-77017cf44e92c18b01e11235ae5dd5a9be9d85de183ba4d936ac86dbb9b009c13</cites><orcidid>0000-0003-3031-5655 ; 0000-0001-5551-6811</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fjgh.15687$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fjgh.15687$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34520088$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lockart, Ian</creatorcontrib><creatorcontrib>Hajarizadeh, Behzad</creatorcontrib><creatorcontrib>Buckley, Niamh</creatorcontrib><creatorcontrib>Davison, Scott</creatorcontrib><creatorcontrib>Prakoso, Emilia</creatorcontrib><creatorcontrib>Levy, Miriam T</creatorcontrib><creatorcontrib>George, Jacob</creatorcontrib><creatorcontrib>Dore, Gregory J</creatorcontrib><creatorcontrib>Danta, Mark</creatorcontrib><title>All‐cause hepatocellular carcinoma survival in the era of direct‐acting antiviral therapy</title><title>Journal of gastroenterology and hepatology</title><addtitle>J Gastroenterol Hepatol</addtitle><description>Background and Aim Hepatitis C virus (HCV) cure with direct‐acting antiviral (DAA) therapy improves survival in patients with HCV‐related hepatocellular carcinoma (HCC). We hypothesized that HCV‐HCC survival has increased in the DAA era, more than other aetiologies of HCC. We aimed to evaluate survival following HCC diagnosis in the pre‐DAA and DAA eras, across each aetiology of HCC. Methods Patients with HCC at three tertiary referral hospitals were included retrospectively (January 2008 to December 2019). Patients were categorized as HCV‐HCC, hepatitis B virus (HBV)‐HCC, or non‐viral HCC. For each aetiology, the risk of death following incident HCC among patients diagnosed in the DAA era (2015–2019) was compared with patients diagnosed in the pre‐DAA era (2008–2014). Results Among 1161 patients, there were 422 (36%) patients with HCV‐HCC, 227 (20%) with HBV‐HCC, and 512 (44%) with non‐viral HCC. In adjusted analysis, the risk of death was lower in patients with HCV‐HCC diagnosed in 2015–2019, compared with patients diagnosed in 2008–2014 (adjusted hazard ratio [aHR]: 0.68; 95% confidence interval [CI]: 0.52–0.89; P = 0.005). In contrast, there was no difference in the risk of death between time periods for patients with HBV‐HCC (HR: 0.91; 95% CI: 0.64–1.29; P = 0.602) or non‐viral HCC on adjusted analysis (aHR: 0.92; 95% CI: 0.74–1.15; P = 0.476). Although patients with HBV‐HCC had better survival compared with patients with HCV‐HCC in 2008–2014 (aHR: 0.74; 95% CI: 0.55–0.98; P = 0.037), this difference disappeared in 2015–2019 (aHR: 1.26; 95% CI: 0.90–1.77; P = 0.175). 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Hajarizadeh, Behzad ; Buckley, Niamh ; Davison, Scott ; Prakoso, Emilia ; Levy, Miriam T ; George, Jacob ; Dore, Gregory J ; Danta, Mark</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3537-77017cf44e92c18b01e11235ae5dd5a9be9d85de183ba4d936ac86dbb9b009c13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Antiviral agents</topic><topic>Antiviral Agents - therapeutic use</topic><topic>Carcinoma, Hepatocellular - mortality</topic><topic>Carcinoma, Hepatocellular - virology</topic><topic>Death</topic><topic>Hepatitis B</topic><topic>Hepatitis C</topic><topic>Hepatitis C, Chronic - complications</topic><topic>Hepatitis C, Chronic - drug therapy</topic><topic>Hepatocellular carcinoma</topic><topic>Humans</topic><topic>Liver cancer</topic><topic>Liver Neoplasms - mortality</topic><topic>Liver Neoplasms - virology</topic><topic>Patients</topic><topic>Retrospective Studies</topic><topic>Survival</topic><topic>Survival Analysis</topic><topic>Viruses</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lockart, Ian</creatorcontrib><creatorcontrib>Hajarizadeh, Behzad</creatorcontrib><creatorcontrib>Buckley, Niamh</creatorcontrib><creatorcontrib>Davison, Scott</creatorcontrib><creatorcontrib>Prakoso, Emilia</creatorcontrib><creatorcontrib>Levy, Miriam T</creatorcontrib><creatorcontrib>George, Jacob</creatorcontrib><creatorcontrib>Dore, Gregory J</creatorcontrib><creatorcontrib>Danta, Mark</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of gastroenterology and hepatology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lockart, Ian</au><au>Hajarizadeh, Behzad</au><au>Buckley, Niamh</au><au>Davison, Scott</au><au>Prakoso, Emilia</au><au>Levy, Miriam T</au><au>George, Jacob</au><au>Dore, Gregory J</au><au>Danta, Mark</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>All‐cause hepatocellular carcinoma survival in the era of direct‐acting antiviral therapy</atitle><jtitle>Journal of gastroenterology and hepatology</jtitle><addtitle>J Gastroenterol Hepatol</addtitle><date>2021-12</date><risdate>2021</risdate><volume>36</volume><issue>12</issue><spage>3515</spage><epage>3523</epage><pages>3515-3523</pages><issn>0815-9319</issn><eissn>1440-1746</eissn><abstract>Background and Aim Hepatitis C virus (HCV) cure with direct‐acting antiviral (DAA) therapy improves survival in patients with HCV‐related hepatocellular carcinoma (HCC). We hypothesized that HCV‐HCC survival has increased in the DAA era, more than other aetiologies of HCC. We aimed to evaluate survival following HCC diagnosis in the pre‐DAA and DAA eras, across each aetiology of HCC. Methods Patients with HCC at three tertiary referral hospitals were included retrospectively (January 2008 to December 2019). Patients were categorized as HCV‐HCC, hepatitis B virus (HBV)‐HCC, or non‐viral HCC. For each aetiology, the risk of death following incident HCC among patients diagnosed in the DAA era (2015–2019) was compared with patients diagnosed in the pre‐DAA era (2008–2014). Results Among 1161 patients, there were 422 (36%) patients with HCV‐HCC, 227 (20%) with HBV‐HCC, and 512 (44%) with non‐viral HCC. In adjusted analysis, the risk of death was lower in patients with HCV‐HCC diagnosed in 2015–2019, compared with patients diagnosed in 2008–2014 (adjusted hazard ratio [aHR]: 0.68; 95% confidence interval [CI]: 0.52–0.89; P = 0.005). In contrast, there was no difference in the risk of death between time periods for patients with HBV‐HCC (HR: 0.91; 95% CI: 0.64–1.29; P = 0.602) or non‐viral HCC on adjusted analysis (aHR: 0.92; 95% CI: 0.74–1.15; P = 0.476). Although patients with HBV‐HCC had better survival compared with patients with HCV‐HCC in 2008–2014 (aHR: 0.74; 95% CI: 0.55–0.98; P = 0.037), this difference disappeared in 2015–2019 (aHR: 1.26; 95% CI: 0.90–1.77; P = 0.175). Conclusions Hepatitis C virus‐related HCC survival has increased in the DAA era, whereas adjusted survival remained stable for HBV‐HCC and non‐viral HCC.</abstract><cop>Australia</cop><pub>Wiley Subscription Services, Inc</pub><pmid>34520088</pmid><doi>10.1111/jgh.15687</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0003-3031-5655</orcidid><orcidid>https://orcid.org/0000-0001-5551-6811</orcidid></addata></record>
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subjects Antiviral agents
Antiviral Agents - therapeutic use
Carcinoma, Hepatocellular - mortality
Carcinoma, Hepatocellular - virology
Death
Hepatitis B
Hepatitis C
Hepatitis C, Chronic - complications
Hepatitis C, Chronic - drug therapy
Hepatocellular carcinoma
Humans
Liver cancer
Liver Neoplasms - mortality
Liver Neoplasms - virology
Patients
Retrospective Studies
Survival
Survival Analysis
Viruses
title All‐cause hepatocellular carcinoma survival in the era of direct‐acting antiviral therapy
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