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PAGE-B predicts the risk of developing hepatocellular carcinoma in Caucasians with chronic hepatitis B on 5-year antiviral therapy

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Autor
Papatheodoridis G., Dalekos G., Sypsa V., Yurdaydin C., Buti M., Goulis J., Calleja J.L., Chi H., Manolakopoulos S., Mangia G., Gatselis N., Keskin O., Savvidou S., De La Revilla J., Hansen B.E., Vlachogiannakos I., Galanis K., Idilman R., Colombo M., Esteban R., Janssen H.L.A., Lampertico P.
Fecha
2016
Language
en
DOI
10.1016/j.jhep.2015.11.035
Materia
entecavir
tenofovir
antivirus agent
entecavir
guanine
tenofovir
adult
age
antiviral therapy
Article
cancer incidence
cancer risk
Caucasian
chronic hepatitis B
controlled study
digestive system disease assessment
female
gender
human
liver cell carcinoma
liver cirrhosis
major clinical study
male
PAGE B score
priority journal
risk assessment
treatment duration
validation process
aged
analogs and derivatives
Carcinoma, Hepatocellular
clinical trial
cohort analysis
complication
Hepatitis B, Chronic
Liver Neoplasms
middle aged
multicenter study
proportional hazards model
risk
Adult
Aged
Antiviral Agents
Carcinoma, Hepatocellular
Cohort Studies
Female
Guanine
Hepatitis B, Chronic
Humans
Liver Neoplasms
Male
Middle Aged
Proportional Hazards Models
Risk
Tenofovir
Elsevier B.V.
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Resumen
Background & Aims Risk scores for hepatocellular carcinoma (HCC) developed in Asians offer poor-moderate predictability in Caucasian patients with chronic hepatitis B (CHB). This nine center cohort study aimed to develop and validate an accurate HCC risk score in Caucasian CHB patients treated with the current oral antivirals, entecavir/tenofovir. Methods We included 1815 adult Caucasians with CHB and no HCC at baseline who received entecavir/tenofovir for ≥12 months. Using data from eight centers (derivation dataset, n = 1325), a HCC risk score was developed based on multivariable Cox models and points system for simplification. Harrell's c-index was used as discrimination, bootstrap for internal validation and the data from the 9th and largest center (validation dataset, n = 490) for external validation. Results The 5-year cumulative HCC incidence rates were 5.7% and 8.4% in the derivation and validation dataset, respectively. In the derivation dataset, age, gender, platelets and cirrhosis were independently associated with HCC. The PAGE-B score was developed based on age, gender and platelets (c-index = 0.82, 0.81 after bootstrap validation). The addition of cirrhosis did not substantially improve the discrimination (c-index = 0.84). The predictability of PAGE-B score was similar (c-index = 0.82) in the validation dataset. Patients with PAGE-B ≤9, 10-17, ≥18 had 5-year cumulative HCC incidence rates of 0%, 3%, 17% in the derivation and 0%, 4%, 16% in the validation dataset. Conclusion PAGE-B, which is based only on baseline patients' age, gender and platelets, represents a simple and reliable score for prediction of the 5-year HCC risk in Caucasian CHB patients under entecavir/tenofovir. © 2015 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.
URI
http://hdl.handle.net/11615/77858
Colecciones
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ. [19735]
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