Baseline serum HBV RNA is associated with the risk of hepatitis flare after stopping nucleoside analog therapy in HBeAg-negative participants.


Journal

Hepatology communications
ISSN: 2471-254X
Titre abrégé: Hepatol Commun
Pays: United States
ID NLM: 101695860

Informations de publication

Date de publication:
01 08 2023
Historique:
received: 06 12 2022
accepted: 11 04 2023
medline: 19 7 2023
pubmed: 17 7 2023
entrez: 17 7 2023
Statut: epublish

Résumé

HBV RNA in peripheral blood reflects HBV cccDNA transcriptional activity and may predict clinical outcomes. The prospective Melbourne HBV-STOP trial studied nucleot(s)ide analog discontinuation in HBeAg-negative non-cirrhotic participants with long-term virological suppression. Ninety-six weeks after stopping treatment, the proportion of participants with virological relapse (HBV DNA > 2000 IU/mL), biochemical relapse (ALT > 2 × ULN and HBV DNA > 2000 IU/mL), or hepatitis flare (ALT > 5 × ULN and HBV DNA > 2000 IU/mL) was 89%, 58%, and 38%, respectively. We evaluated the ability of serum HBV RNA levels to predict these outcomes. HBV RNA levels were measured using the Roche cobas 6800/8800 HBV RNA Investigational Assay. Sixty-five participants had baseline and longitudinal off-treatment specimens available for RNA testing. HBV RNA was detectable at baseline in 25% of participants and was associated with a higher risk of biochemical relapse (81% vs. 51%, p value 0.04) and hepatitis flare (63% vs. 31%, p value 0.04). Participants who had undetectable serum HBV RNA as well as HBsAg ≤ 100 IU/mL at baseline were less likely to experience virological relapse (4 of 9, 44%) than participants with detectable HBV RNA and HBsAg level > 100 IU/mL (15/15, 100%; p value 0.0009). Off-treatment levels of HBV RNA were correlated with HBV DNA and were associated with the risk of hepatitis flare. Serum HBV RNA may be a useful biomarker for guiding clinical decision-making before stopping nucleot(s)ide analog therapy. Baseline HBV RNA and HBsAg levels are associated with the risk of clinical relapse, hepatitis flare, and disease remission off-treatment.

Sections du résumé

BACKGROUND AND AIMS
HBV RNA in peripheral blood reflects HBV cccDNA transcriptional activity and may predict clinical outcomes. The prospective Melbourne HBV-STOP trial studied nucleot(s)ide analog discontinuation in HBeAg-negative non-cirrhotic participants with long-term virological suppression. Ninety-six weeks after stopping treatment, the proportion of participants with virological relapse (HBV DNA > 2000 IU/mL), biochemical relapse (ALT > 2 × ULN and HBV DNA > 2000 IU/mL), or hepatitis flare (ALT > 5 × ULN and HBV DNA > 2000 IU/mL) was 89%, 58%, and 38%, respectively. We evaluated the ability of serum HBV RNA levels to predict these outcomes.
APPROACH RESULTS
HBV RNA levels were measured using the Roche cobas 6800/8800 HBV RNA Investigational Assay. Sixty-five participants had baseline and longitudinal off-treatment specimens available for RNA testing. HBV RNA was detectable at baseline in 25% of participants and was associated with a higher risk of biochemical relapse (81% vs. 51%, p value 0.04) and hepatitis flare (63% vs. 31%, p value 0.04). Participants who had undetectable serum HBV RNA as well as HBsAg ≤ 100 IU/mL at baseline were less likely to experience virological relapse (4 of 9, 44%) than participants with detectable HBV RNA and HBsAg level > 100 IU/mL (15/15, 100%; p value 0.0009). Off-treatment levels of HBV RNA were correlated with HBV DNA and were associated with the risk of hepatitis flare.
CONCLUSIONS
Serum HBV RNA may be a useful biomarker for guiding clinical decision-making before stopping nucleot(s)ide analog therapy. Baseline HBV RNA and HBsAg levels are associated with the risk of clinical relapse, hepatitis flare, and disease remission off-treatment.

Identifiants

pubmed: 37459199
doi: 10.1097/HC9.0000000000000188
pii: 02009842-202308010-00004
pmc: PMC10351945
pii:
doi:

Substances chimiques

Antiviral Agents 0
DNA, Viral 0
Hepatitis B e Antigens 0
Hepatitis B Surface Antigens 0
Nucleosides 0
RNA 63231-63-0

Types de publication

Clinical Trial Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2023 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Association for the Study of Liver Diseases.

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Auteurs

Alexander J Thompson (AJ)

Department of Gastroenterology, St Vincent's Hospital Melbourne, Melbourne, Victoria, Australia.
Immunology Research Centre, Department of Medicine (St Vincent's Hospital), The University of Melbourne, Melbourne, Victoria, Australia.

Kathy Jackson (K)

Victorian Infectious Diseases Reference Laboratory, Royal Melbourne Hospital, Doherty Institute for Infection and Immunity, Melbourne, Victoria, Australia.

Sara Bonanzinga (S)

Victorian Infectious Diseases Reference Laboratory, Royal Melbourne Hospital, Doherty Institute for Infection and Immunity, Melbourne, Victoria, Australia.

Sam A L Hall (SAL)

Department of Gastroenterology, St Vincent's Hospital Melbourne, Melbourne, Victoria, Australia.
Immunology Research Centre, Department of Medicine (St Vincent's Hospital), The University of Melbourne, Melbourne, Victoria, Australia.

Simon Hume (S)

Department of Gastroenterology, St Vincent's Hospital Melbourne, Melbourne, Victoria, Australia.
Immunology Research Centre, Department of Medicine (St Vincent's Hospital), The University of Melbourne, Melbourne, Victoria, Australia.

Gareth S Burns (GS)

Department of Gastroenterology, St Vincent's Hospital Melbourne, Melbourne, Victoria, Australia.
Immunology Research Centre, Department of Medicine (St Vincent's Hospital), The University of Melbourne, Melbourne, Victoria, Australia.

Vijaya Sundararajan (V)

Immunology Research Centre, Department of Medicine (St Vincent's Hospital), The University of Melbourne, Melbourne, Victoria, Australia.
Department of Public Health, La Trobe University, Melbourne, Victoria, Australia.

Dilip Ratnam (D)

Gastroenterology & Hepatology Unit, Monash Health, Melbourne, Victoria, Australia.
Monash University, Melbourne, Victoria, Australia.

Miriam T Levy (MT)

Department of Gastroenterology and Hepatology, Liverpool Hospital, Sydney, Australia.

John Lubel (J)

Department of Gastroenterology, Alfred Health, Melbourne, Victoria, Australia.
Central Clinical School, Monash University, The Alfred Centre, Melbourne, Victoria, Australia.

Amanda J Nicoll (AJ)

Gastroenterology Department of Eastern Health, Melbourne, Victoria, Australia.

Simone I Strasser (SI)

AW Morrow Gastroenterology and Liver Centre, Royal Prince Alfred Hospital, Sydney, Australia.
University of Sydney, Sydney, Australia.

William Sievert (W)

Gastroenterology & Hepatology Unit, Monash Health, Melbourne, Victoria, Australia.
Monash University, Melbourne, Victoria, Australia.

Paul V Desmond (PV)

Department of Gastroenterology, St Vincent's Hospital Melbourne, Melbourne, Victoria, Australia.

Meng C Ngu (MC)

Department of Gastroenterology, Concord Repatriation General Hospital, Sydney, Australia.

Marie Sinclair (M)

Department of Gastroenterology and Hepatology, Austin Health, Melbourne, Victoria, Australia.

Christopher Meredith (C)

Department of Gastroenterology, Bankstown-Lidcombe Hospital, Sydney, Australia.

Gail Matthews (G)

Department of Infectious Disease, St Vincent's Hospital Sydney, Sydney, Australia.

Peter A Revill (PA)

Victorian Infectious Diseases Reference Laboratory, Royal Melbourne Hospital, Doherty Institute for Infection and Immunity, Melbourne, Victoria, Australia.

Margaret Littlejohn (M)

Victorian Infectious Diseases Reference Laboratory, Royal Melbourne Hospital, Doherty Institute for Infection and Immunity, Melbourne, Victoria, Australia.

D Scott Bowden (DS)

Victorian Infectious Diseases Reference Laboratory, Royal Melbourne Hospital, Doherty Institute for Infection and Immunity, Melbourne, Victoria, Australia.

Jesse A Canchola (JA)

Roche Molecular Systems, Inc., Pleasanton, California, USA.

Jason Torres (J)

Roche Molecular Systems, Inc., Pleasanton, California, USA.

Philip Siew (P)

Roche Diagnostics, Pty Ltd, North Ryde, Australia.

Jasmin Lau (J)

Roche Molecular Systems, Inc., Pleasanton, California, USA.

Benjamin La Brot (B)

Roche Molecular Systems, Inc., Pleasanton, California, USA.

Alison Kuchta (A)

Roche Molecular Systems, Inc., Pleasanton, California, USA.

Kumar Visvanathan (K)

Victorian Infectious Diseases Reference Laboratory, Royal Melbourne Hospital, Doherty Institute for Infection and Immunity, Melbourne, Victoria, Australia.

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