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dc.creatorPapatheodoridis G.V., Sypsa V., Dalekos G.N., Yurdaydin C., Van Boemmel F., Buti M., Calleja J.L., Chi H., Goulis J., Manolakopoulos S., Loglio A., Voulgaris T., Gatselis N., Keskin O., Veelken R., Lopez-Gomez M., Hansen B.E., Savvidou S., Kourikou A., Vlachogiannakos J., Galanis K., Idilman R., Esteban R., Janssen H.L.A., Berg T., Lampertico P.en
dc.date.accessioned2023-01-31T09:44:57Z
dc.date.available2023-01-31T09:44:57Z
dc.date.issued2020
dc.identifier10.1016/j.jhep.2020.01.007
dc.identifier.issn01688278
dc.identifier.urihttp://hdl.handle.net/11615/77866
dc.description.abstractBackground & Aims: Hepatocellular carcinoma (HCC) may develop in patients with chronic hepatitis (CHB) even after 5 years of oral therapy and cannot be easily predicted. We assessed predictors of HCC development and the need for HCC surveillance in this setting. Methods: Of 1,951 adult Caucasians with CHB included in the PAGE-B cohort, 1,427 (73%) had completed >5 years of follow-up under therapy without developing HCC by year 5. Median follow-up was 8.4 years from treatment onset. Points-based risk scores were developed to predict HCC risk after year 5. Results: In years 5–12, HCC was diagnosed in 33/1,427 (2.3%) patients with cumulative incidences of 2.4%, 3.2% and 3.8% at 8, 10 and 12 years, respectively. Older age or age >50 years, baseline cirrhosis and liver stiffness (LSM) ≥12 kPa at year 5 were independently associated with increased HCC risk. The HCC incidence was lower in non-cirrhotics than cirrhotics at baseline with year-5 LSM <12; among cirrhotics at baseline, it was lower in those with year-5 LSM <12 than ≥12 kPa. CAGE-B score was based on age at year 5 and baseline cirrhosis in relation to LSM at year 5 and SAGE-B score was based only on age and LSM at year 5 (c-index = 0.809–0.814, 0.805–0.806 after bootstrap validation). Both scores offered 100% negative predictive values for HCC development in their low risk groups. Conclusions: In Caucasians with CHB, the HCC risk after the first 5 years of antiviral therapy depends on age, baseline cirrhosis status and LSM at year 5. CAGE-B and particularly SAGE-B represent simple and reliable risk scores for HCC prediction and surveillance beyond year 5 of therapy. Lay summary: In Caucasians with chronic hepatitis B, the risk of hepatocellular carcinoma after the first 5 years of entecavir or tenofovir therapy depends on age, baseline cirrhosis status and liver stiffness at year 5, which can provide simple and reliable risk scores for hepatocellular carcinoma prediction and surveillance beyond year 5. In patients with cirrhosis at baseline, liver stiffness <12 kPa at year 5 is associated with lower HCC risk, but surveillance may be still required. © 2020 European Association for the Study of the Liveren
dc.language.isoenen
dc.sourceJournal of Hepatologyen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85081282634&doi=10.1016%2fj.jhep.2020.01.007&partnerID=40&md5=6c606b5692dfb744711a81e77ec5d048
dc.subjectadulten
dc.subjectArticleen
dc.subjectCAGE B scoreen
dc.subjectcancer risken
dc.subjectCaucasianen
dc.subjectchronic hepatitis Ben
dc.subjectfemaleen
dc.subjectfollow upen
dc.subjecthumanen
dc.subjectliver cell carcinomaen
dc.subjectliver cirrhosisen
dc.subjectliver stiffnessen
dc.subjectmajor clinical studyen
dc.subjectmaleen
dc.subjectmiddle ageden
dc.subjectpredictionen
dc.subjectpriority journalen
dc.subjectSAGE B scoreen
dc.subjectscoring systemen
dc.subjectageden
dc.subjectblooden
dc.subjectCaucasianen
dc.subjectchronic hepatitis Ben
dc.subjectclinical trialen
dc.subjectcomplicationen
dc.subjectethnologyen
dc.subjectgeneticsen
dc.subjectHepatitis B virusen
dc.subjectincidenceen
dc.subjectliver cell carcinomaen
dc.subjectliver tumoren
dc.subjectmulticenter studyen
dc.subjectoral drug administrationen
dc.subjectrisk factoren
dc.subjecttreatment outcomeen
dc.subjectvirologyen
dc.subjectyoung adulten
dc.subjectantivirus agenten
dc.subjectentecaviren
dc.subjectguanineen
dc.subjecthepatitis B surface antigenen
dc.subjecttenofoviren
dc.subjectvirus DNAen
dc.subjectAdministration, Oralen
dc.subjectAdulten
dc.subjectAgeden
dc.subjectAntiviral Agentsen
dc.subjectCarcinoma, Hepatocellularen
dc.subjectDNA, Viralen
dc.subjectEuropean Continental Ancestry Groupen
dc.subjectFemaleen
dc.subjectFollow-Up Studiesen
dc.subjectGuanineen
dc.subjectHepatitis B Surface Antigensen
dc.subjectHepatitis B virusen
dc.subjectHepatitis B, Chronicen
dc.subjectHumansen
dc.subjectIncidenceen
dc.subjectLiver Cirrhosisen
dc.subjectLiver Neoplasmsen
dc.subjectMaleen
dc.subjectMiddle Ageden
dc.subjectRisk Factorsen
dc.subjectTenofoviren
dc.subjectTreatment Outcomeen
dc.subjectYoung Adulten
dc.subjectElsevier B.V.en
dc.titleHepatocellular carcinoma prediction beyond year 5 of oral therapy in a large cohort of Caucasian patients with chronic hepatitis Ben
dc.typejournalArticleen


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