Entecavir Reduced Serum Hepatitis B Core-Related Antigen in Chronic Hepatitis B Patients with Hepatocellular Carcinoma.


Journal

Gut and liver
ISSN: 2005-1212
Titre abrégé: Gut Liver
Pays: Korea (South)
ID NLM: 101316452

Informations de publication

Date de publication:
15 09 2020
Historique:
received: 13 12 2019
revised: 12 02 2020
accepted: 01 03 2020
pubmed: 28 5 2020
medline: 14 9 2021
entrez: 28 5 2020
Statut: ppublish

Résumé

Serum hepatitis B core-related antigen (HBcrAg) was shown to predict the risk of hepatocellular carcinoma (HCC) in chronic hepatitis B (CHB) patients undergoing treatment. We investigated the longitudinal profile of HBcrAg in entecavir (ETV)-treated CHB patients with subsequent HCC development. We identified HCC cases diagnosed at ≥1 year after ETV initiation. CHB patients without HCC (matched for age, sex, cirrhosis status, baseline hepatitis B virus [HBV] DNA level, and ETV treatment duration) were identified as controls at an HCC:non-HCC ratio of 1:2. Serum samples were retrieved at baseline (ETV initiation) and at 3 and 5 years of ETV therapy for HBcrAg measurement (log IU/mL). In total, 180 patients (60 HCC patients matched with 120 CHB patients without HCC; median age, 56.5 years; 80.6% male; baseline HBV DNA, 5.9 log IU/mL; median follow-up, 6.8 years) were recruited. The median time from ETV initiation to HCC development was 3.2 years. HBcrAg levels were higher in HCC cases than in controls at all three time points: 5.69 log IU/ mL versus 5.02 log IU/mL (p=0.025), 4.23 log IU/mL versus 3.36 log IU/mL (p=0.007), and 3.86 log IU/mL versus 3.36 log IU/mL (p=0.009), respectively. ETV led to similar rates of decline in HBcrAg from baseline to 3 years in both groups (0.34 log IU/mL/year vs 0.39 log IU/mL/year, p=0.774), although the decline from 3 to 5 years was slower in the non- HCC group (0.05 log IU/mL/year) than in the HCC group (0.09 log IU/mL/year, p=0.055). ETV time-dependently reduced HBcrAg in HCC and non-HCC patients. HBcrAg interpretation should consider the antiviral treatment duration.

Identifiants

pubmed: 32457279
pii: gnl19434
doi: 10.5009/gnl19434
pmc: PMC7492492
doi:

Substances chimiques

Antiviral Agents 0
Biomarkers 0
DNA, Viral 0
Hepatitis B Core Antigens 0
Hepatitis B e Antigens 0
entecavir 5968Y6H45M
Guanine 5Z93L87A1R

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

665-668

Références

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pubmed: 17483190
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pubmed: 17942661
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J Infect Dis. 2016 Apr 1;213(7):1096-106
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pubmed: 29072673
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pubmed: 15185311
J Hepatol. 2017 Feb;66(2):275-281
pubmed: 27639844
Clin Mol Hepatol. 2016 Sep;22(3):319-326
pubmed: 27729632
JAMA. 2006 Jan 4;295(1):65-73
pubmed: 16391218
Aliment Pharmacol Ther. 2019 Feb;49(4):457-471
pubmed: 30663078
J Viral Hepat. 2017 Aug;24(8):654-661
pubmed: 28185363
J Hepatol. 2015 Apr;62(4):956-67
pubmed: 25595883
Gut. 2011 Aug;60(8):1109-16
pubmed: 21270118
J Hepatol. 2017 Aug;67(2):370-398
pubmed: 28427875

Auteurs

Lung-Yi Mak (LY)

Department of Medicine, Queen Mary Hospital, The University of Hong Kong, China.

Kwan-Lung Ko (KL)

Department of Medicine, Queen Mary Hospital, The University of Hong Kong, China.

Wai-Pan To (WP)

Department of Medicine, Queen Mary Hospital, The University of Hong Kong, China.

Danny Ka-Ho Wong (DK)

Department of Medicine, Queen Mary Hospital, The University of Hong Kong, China.
State Key Laboratory of Liver Research, The University of Hong Kong, Hong Kong, China.

Wai-Kay Seto (WK)

Department of Medicine, Queen Mary Hospital, The University of Hong Kong, China.
State Key Laboratory of Liver Research, The University of Hong Kong, Hong Kong, China.
Department of Medicine, The University of Hong Kong-Shenzhen Hospital, Shenzhen, China.

James Fung (J)

Department of Medicine, Queen Mary Hospital, The University of Hong Kong, China.
State Key Laboratory of Liver Research, The University of Hong Kong, Hong Kong, China.

Man-Fung Yuen (MF)

Department of Medicine, Queen Mary Hospital, The University of Hong Kong, China.
State Key Laboratory of Liver Research, The University of Hong Kong, Hong Kong, China.

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Classifications MeSH