{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,18]],"date-time":"2026-08-18T01:13:58Z","timestamp":1787015638015,"version":"build-2736575974"},"reference-count":32,"publisher":"Wiley","issue":"12","license":[{"start":{"date-parts":[[2016,10,4]],"date-time":"2016-10-04T00:00:00Z","timestamp":1475539200000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"funder":[{"DOI":"10.13039\/100001009","name":"Bristol-Myers Squibb Foundation","doi-asserted-by":"publisher","id":[{"id":"10.13039\/100001009","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/501100004737","name":"National Health Research Institutes","doi-asserted-by":"publisher","award":["NHRI\u2010EX103\u201010319PC"],"award-info":[{"award-number":["NHRI\u2010EX103\u201010319PC"]}],"id":[{"id":"10.13039\/501100004737","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Liver International"],"published-print":{"date-parts":[[2016,12]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:sec>\n                    <jats:title>Background &amp; Aims<\/jats:title>\n                    <jats:p>\n                      Oral antiviral therapy may reduce the disease progression of chronic hepatitis B (\n                      <jats:styled-content style=\"fixed-case\">CHB<\/jats:styled-content>\n                      ) patients. We aimed to further investigate the efficacy of long\u2010term entecavir therapy in reduction of the risk of hepatocellular carcinoma (\n                      <jats:styled-content style=\"fixed-case\">HCC<\/jats:styled-content>\n                      ), cirrhotic events and mortality in a large group of\n                      <jats:styled-content style=\"fixed-case\">CHB<\/jats:styled-content>\n                      \u2010related cirrhosis patients.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methods<\/jats:title>\n                    <jats:p>\n                      The C\u2010\n                      <jats:styled-content style=\"fixed-case\">TEAM<\/jats:styled-content>\n                      (Cirrhosis\u2010Taiwanese EntecAvir Multicenter) study was a nationwide, multicenter, retrospective\u2013prospective cohort study in Taiwan. We enrolled treatment\u2010na\u00efve patients with\n                      <jats:styled-content style=\"fixed-case\">CHB<\/jats:styled-content>\n                      \u2010related cirrhosis and baseline\n                      <jats:styled-content style=\"fixed-case\">HBV<\/jats:styled-content>\n                      \u2010\n                      <jats:styled-content style=\"fixed-case\">DNA<\/jats:styled-content>\n                      \u22652000\u00a0IU\/mL receiving long\u2010term entecavir therapy and compared the development of\n                      <jats:styled-content style=\"fixed-case\">HCC<\/jats:styled-content>\n                      , cirrhotic events and mortality with that of a historical untreated cohort.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      In total, 1315 entecavir\u2010treated and 503 untreated patients with cirrhosis were enrolled, with median treatment and follow\u2010up durations of 4 and 6\u00a0years respectively. Compared with the untreated cohort, entecavir therapy was associated with a 60%\n                      <jats:styled-content style=\"fixed-case\">HCC<\/jats:styled-content>\n                      risk reduction [hazard ratio (\n                      <jats:styled-content style=\"fixed-case\">HR<\/jats:styled-content>\n                      ): 0.40, 95% confidence interval (\n                      <jats:styled-content style=\"fixed-case\">CI<\/jats:styled-content>\n                      ): 0.28\u20100.57]. Additionally, an older age, the male gender,\n                      <jats:styled-content style=\"fixed-case\">HBeA<\/jats:styled-content>\n                      g positivity, alpha\u2010fetoprotein (\n                      <jats:styled-content style=\"fixed-case\">AFP<\/jats:styled-content>\n                      )\u22657\u00a0ng\/mL before therapy were independent predictors of\n                      <jats:styled-content style=\"fixed-case\">HCC<\/jats:styled-content>\n                      development. Further analysis showed that entecavir therapy significantly reduced risks of variceal bleeding, spontaneous bacterial peritonitis, and liver\u2010related and all\u2010cause mortality. These findings were confirmed by propensity score\u2010matched cohorts in sensitivity analysis. In patients under entecavir therapy, an older age, the male gender,\n                      <jats:styled-content style=\"fixed-case\">HBeA<\/jats:styled-content>\n                      g positivity,\n                      <jats:styled-content style=\"fixed-case\">AFP<\/jats:styled-content>\n                      level \u22657\u00a0ng\/mL before therapy, and 1\u2010year virological response were predictive of\n                      <jats:styled-content style=\"fixed-case\">HCC<\/jats:styled-content>\n                      development.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusions<\/jats:title>\n                    <jats:p>\n                      Four\u2010year entecavir therapy significantly reduces the risk of\n                      <jats:styled-content style=\"fixed-case\">HCC<\/jats:styled-content>\n                      , cirrhotic events and mortality in patients with\n                      <jats:styled-content style=\"fixed-case\">CHB<\/jats:styled-content>\n                      \u2010related cirrhosis.\n                    <\/jats:p>\n                  <\/jats:sec>","DOI":"10.1111\/liv.13253","type":"journal-article","created":{"date-parts":[[2016,9,16]],"date-time":"2016-09-16T05:29:49Z","timestamp":1474003789000},"page":"1755-1764","source":"Crossref","is-referenced-by-count":196,"title":["Four\u2010year entecavir therapy reduces hepatocellular carcinoma, cirrhotic events and mortality in chronic hepatitis B patients"],"prefix":"10.1111","volume":"36","author":[{"given":"Tung\u2010Hung","family":"Su","sequence":"first","affiliation":[{"name":"Department of Internal Medicine National Taiwan University Hospital  Taipei Taiwan"},{"name":"Graduate Institute of Clinical Medicine National Taiwan University College of Medicine  Taipei 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