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Excellent safety and effectiveness of high-dose myrcludex-B monotherapy administered for 48 weeks in HDV-related compensated cirrhosis: A case report of 3 patients.
- Source :
-
Journal of hepatology [J Hepatol] 2019 Oct; Vol. 71 (4), pp. 834-839. Date of Electronic Publication: 2019 Jul 11. - Publication Year :
- 2019
-
Abstract
- Short-term administration of the entry inhibitor myrcludex-B (MyrB) has been shown to be safe and effective in phase II studies in patients coinfected with hepatitis B virus (HBV) and hepatitis delta virus (HDV). However, its effectiveness and safety are unknown during long-term and high-dose treatment of patients with compensated cirrhosis in real-life settings. Herein, we describe the first 3 European patients with HDV-related compensated cirrhosis who were treated with MyrB 10 mg/day for 48 weeks as a compassionate therapy. Liver function tests, bile acids, and virological markers were monitored every 4 weeks. HBV/HDV-specific T cell quantity (up to 48 and 36 weeks) and HBV RNA levels were also assessed in 2 cases. During MyrB treatment, HDV RNA levels progressively declined from 4.4 and 5.6 logs IU/ml to undetectability in 2 cases, and from 6.8 log copies/ml to 500 copies/ml for the other patient. Alanine aminotransferase normalised after 20, 12 and 28 weeks, respectively. A significant improvement in features of portal hypertension, liver function tests and alpha-fetoprotein levels were documented in 2 cases. In the male patient with histological and clinical stigmata of autoimmune hepatitis, IgG and immunoglobulins rapidly normalised. No significant changes in HBV surface antigen levels and circulating HBV/HDV-specific T cells were demonstrated; HBV DNA and HBV RNA levels remained undetectable throughout the study period. MyrB was well tolerated; patients remained fully asymptomatic despite a significant increase of bile acids. In conclusion, this report shows excellent safety and effectiveness of a 48-week course of MyrB 10 mg/day, combined with tenofovir disoproxil fumarate, for the treatment of HDV-related compensated cirrhosis.<br /> (Copyright © 2019 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.)
- Subjects :
- Aged
Antiviral Agents administration & dosage
Antiviral Agents adverse effects
Coinfection drug therapy
Dose-Response Relationship, Drug
Drug Monitoring methods
Drug Therapy, Combination
Duration of Therapy
Female
Humans
Liver Function Tests methods
Male
Middle Aged
Patient Acuity
RNA, Viral isolation & purification
Treatment Outcome
Hepatitis B virus drug effects
Hepatitis B virus genetics
Hepatitis B virus isolation & purification
Hepatitis B, Chronic blood
Hepatitis B, Chronic physiopathology
Hepatitis B, Chronic therapy
Hepatitis D blood
Hepatitis D physiopathology
Hepatitis D therapy
Hepatitis D virology
Hepatitis Delta Virus drug effects
Hepatitis Delta Virus genetics
Hepatitis Delta Virus isolation & purification
Lipopeptides administration & dosage
Liver Cirrhosis blood
Liver Cirrhosis therapy
Liver Cirrhosis virology
Tenofovir administration & dosage
Tenofovir adverse effects
Subjects
Details
- Language :
- English
- ISSN :
- 1600-0641
- Volume :
- 71
- Issue :
- 4
- Database :
- MEDLINE
- Journal :
- Journal of hepatology
- Publication Type :
- Academic Journal
- Accession number :
- 31302176
- Full Text :
- https://doi.org/10.1016/j.jhep.2019.07.003