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  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
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  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
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Hepatocellular carcinoma prediction beyond year 5 of oral therapy in a large cohort of Caucasian patients with chronic hepatitis B

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Auteur
Papatheodoridis 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.
Date
2020
Language
en
DOI
10.1016/j.jhep.2020.01.007
Sujet
adult
Article
CAGE B score
cancer risk
Caucasian
chronic hepatitis B
female
follow up
human
liver cell carcinoma
liver cirrhosis
liver stiffness
major clinical study
male
middle aged
prediction
priority journal
SAGE B score
scoring system
aged
blood
Caucasian
chronic hepatitis B
clinical trial
complication
ethnology
genetics
Hepatitis B virus
incidence
liver cell carcinoma
liver tumor
multicenter study
oral drug administration
risk factor
treatment outcome
virology
young adult
antivirus agent
entecavir
guanine
hepatitis B surface antigen
tenofovir
virus DNA
Administration, Oral
Adult
Aged
Antiviral Agents
Carcinoma, Hepatocellular
DNA, Viral
European Continental Ancestry Group
Female
Follow-Up Studies
Guanine
Hepatitis B Surface Antigens
Hepatitis B virus
Hepatitis B, Chronic
Humans
Incidence
Liver Cirrhosis
Liver Neoplasms
Male
Middle Aged
Risk Factors
Tenofovir
Treatment Outcome
Young Adult
Elsevier B.V.
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Résumé
Background & 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 Liver
URI
http://hdl.handle.net/11615/77866
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  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ. [19735]

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