TY - JOUR
T1 - Effectiveness and Safety of Entecavir or Tenofovir in a Spanish Cohort of Chronic Hepatitis B Patients: Validation of the Page-B Score to Predict Hepatocellular Carcinoma
AU - Riveiro-Barciela, Mar
AU - Tabernero, David
AU - Calleja, José L.
AU - Lens, Sabela
AU - Manzano, María L.
AU - Rodríguez, Francisco Gea
AU - Crespo, Javier
AU - Piqueras, Belén
AU - Pascasio, Juan M.
AU - Comas, Carmen
AU - Gutierrez, Maria L.
AU - Aguirre, Alberto
AU - Suárez, Emilio
AU - García-Samaniego, Javier
AU - Rivero, Miguel
AU - Acero, Doroteo
AU - Fernandez-Bermejo, Miguel
AU - Moreno, Diego
AU - Sánchez-Pobre, Pilar
AU - de Cuenca, Beatriz
AU - Moreno-Palomares, J. J.
AU - Esteban, Rafael
AU - Buti, Maria
PY - 2017/3/1
Y1 - 2017/3/1
N2 - © 2017, Springer Science+Business Media New York. Background: Long-term antiviral therapy has resulted in viral suppression and biochemical response in chronic hepatitis B, although the risk of hepatocellular carcinoma has not been abolished. The Page-B score could be useful to estimate the probability of HCC. Aims: To analyze the effectiveness and safety of entecavir or tenofovir for more than 4 years and the usefulness of Page-B score in the real-world setting. Methods: Analysis of Caucasian chronic hepatitis B subjects treated with entecavir or tenofovir from the prospective, multicenter database CIBERHEP. Results: A total of 611 patients were enrolled: 187 received entecavir and 424 tenofovir. Most were men, mean age 50 years, 32% cirrhotic and 16.5% HBeAg-positive. Mean follow-up was 55 (entecavir) and 49 (tenofovir) months. >90% achieved HBV DNA <69 IU/mL and biochemical normalization by months 12 and 36, respectively. Cumulative HBeAg loss and anti-HBe seroconversion were achieved by 33.7 and 23.8%. Four patients lost HBsAg; three HBeAg-positive. Renal function remained stable on long-term follow-up. Fourteen (2.29%) developed HCC during follow-up all of them with baseline Page-B ≥10. Nine were diagnosed within the first 5 years of therapy. This contrasts with the 27 estimated by Page-B, a difference that highlights the importance of regular HCC surveillance even in patients with virological suppression. Conclusions: Entecavir and tenofovir achieved high biochemical and virological response. Renal function remained stable with both drugs. A Page-B cut-off ≥10 selected all patients at risk of HCC development.
AB - © 2017, Springer Science+Business Media New York. Background: Long-term antiviral therapy has resulted in viral suppression and biochemical response in chronic hepatitis B, although the risk of hepatocellular carcinoma has not been abolished. The Page-B score could be useful to estimate the probability of HCC. Aims: To analyze the effectiveness and safety of entecavir or tenofovir for more than 4 years and the usefulness of Page-B score in the real-world setting. Methods: Analysis of Caucasian chronic hepatitis B subjects treated with entecavir or tenofovir from the prospective, multicenter database CIBERHEP. Results: A total of 611 patients were enrolled: 187 received entecavir and 424 tenofovir. Most were men, mean age 50 years, 32% cirrhotic and 16.5% HBeAg-positive. Mean follow-up was 55 (entecavir) and 49 (tenofovir) months. >90% achieved HBV DNA <69 IU/mL and biochemical normalization by months 12 and 36, respectively. Cumulative HBeAg loss and anti-HBe seroconversion were achieved by 33.7 and 23.8%. Four patients lost HBsAg; three HBeAg-positive. Renal function remained stable on long-term follow-up. Fourteen (2.29%) developed HCC during follow-up all of them with baseline Page-B ≥10. Nine were diagnosed within the first 5 years of therapy. This contrasts with the 27 estimated by Page-B, a difference that highlights the importance of regular HCC surveillance even in patients with virological suppression. Conclusions: Entecavir and tenofovir achieved high biochemical and virological response. Renal function remained stable with both drugs. A Page-B cut-off ≥10 selected all patients at risk of HCC development.
KW - Effectiveness
KW - Entecavir
KW - Hepatitis B
KW - Hepatocellular carcinoma
KW - Page-B
KW - Safety
KW - Tenofovir
U2 - 10.1007/s10620-017-4448-7
DO - 10.1007/s10620-017-4448-7
M3 - Article
SN - 0163-2116
VL - 62
SP - 784
EP - 793
JO - Digestive Diseases and Sciences
JF - Digestive Diseases and Sciences
IS - 3
ER -