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Daring-B: Discontinuation of effective entecavir or tenofovir disoproxil fumarate long-term therapy before HBsAg loss in non-cirrhotic HBeAg-negative chronic hepatitis B

Thumbnail
Autore
Papatheodoridis G.V., Rigopoulou E.I., Papatheodoridi M., Zachou K., Xourafas V., Gatselis N., Hadziyannis E., Vlachogiannakos J., Manolakopoulos S., Dalekos G.N.
Data
2018
Language
en
DOI
10.3851/IMP3256
Soggetto
alanine aminotransferase
entecavir
hepatitis B surface antigen
hepatitis B(e) antigen
tenofovir disoproxil
virus DNA
entecavir
guanine
hepatitis B surface antigen
hepatitis B(e) antigen
tenofovir
adult
Article
chronic drug administration
chronic hepatitis B
controlled study
death
decompensated liver cirrhosis
disease severity
drug efficacy
drug withdrawal
female
follow up
human
human cell
human tissue
jaundice
liver cirrhosis
liver fibrosis
major clinical study
male
prediction
priority journal
probability
prospective study
recurrence risk
reference value
relapse
remission
retreatment
treatment response
aged
blood
chronic hepatitis B
Hepatitis B virus
immunology
liver function test
middle aged
proportional hazards model
recurrent disease
treatment outcome
virology
virus load
Adult
Aged
Female
Follow-Up Studies
Guanine
Hepatitis B e Antigens
Hepatitis B Surface Antigens
Hepatitis B virus
Hepatitis B, Chronic
Humans
Liver Function Tests
Male
Middle Aged
Proportional Hazards Models
Recurrence
Retreatment
Tenofovir
Treatment Outcome
Viral Load
International Medical Press Ltd
Mostra tutti i dati dell'item
Abstract
Background: The remission rates after stopping antivirals in hepatitis B e antigen (HBeAg)-negative chronic hepatitis B (CHB) vary among studies, while reliable predictors of relapse have not been identified. This prospective study assessed rates and predictors of relapse and retreatment in 57 non-cirrhotic hepatitis B surface antigen (HBsAg)positive patients with HBeAg-negative CHB who discontinued effective ≥4-year entecavir or tenofovir disoproxil fumarate (TDF) therapy. Methods: A total of 57 patients discontinued therapy after median virological remission of 5.3 years and remained under close follow-up. They were retreated with entecavir/TDF if they fulfilled predetermined criteria. Results: During median follow-up of 18 months, no patient died, developed jaundice or liver decompensation. The cumulative relapse rates varied according to HBV DNA and alanine aminotransferase cutoffs; for HBV DNA >2,000 IU/ml, they were 56%, 70% and 72% at 3, 12 and 18 months after stopping entecavir/TDF. The cumulative probability of retreatment was 18% and 26% at 3 and 12 months being significantly affected only by pretreatment fibrosis severity (adjusted relative hazard: 3.43; P=0.015). Cumulative rates of HBsAg loss were 5%, 16% and 25% at 6, 12 and 18 months being higher in patients with lower HBsAg levels at treatment discontinuation. Conclusions: Our prospective study shows that effective ≥4-year entecavir/TDF therapy can be safely discontinued in non-cirrhotic HBeAg-negative CHB patients. The probability of relapse decreased after month 6. Despite common virological relapses, most patients, particularly those with mild–moderate pretreatment fibrosis, remain without retreatment, at least in the first 18 months, as a substantial proportion of them clear HBsAg and the majority eventually enters into an inactive carrier state. ©2018 International Medical Press.
URI
http://hdl.handle.net/11615/77864
Collections
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ. [19735]

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