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Rapid monophasic HBsAg decline during nucleic-acid polymer–based therapy predicts functional cure

Analyzing the interplay among serum HBV DNA, HBsAg, anti-HBs, and alanine aminotransferase (ALT) during nucleic-acid polymer (NAP)-based therapy for chronic hepatitis B provides a unique opportunity to identify kinetic patterns associated with functional cure. METHODS: All participants with HBeAg-ne...

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Autores principales: Hershkovich, Leeor, Shekhtman, Louis, Bazinet, Michel, Pântea, Victor, Placinta, Gheorge, Cotler, Scott J., Vaillant, Andrew, Dahari, Harel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10351942/
https://www.ncbi.nlm.nih.gov/pubmed/37458583
http://dx.doi.org/10.1097/HC9.0000000000000205
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author Hershkovich, Leeor
Shekhtman, Louis
Bazinet, Michel
Pântea, Victor
Placinta, Gheorge
Cotler, Scott J.
Vaillant, Andrew
Dahari, Harel
author_facet Hershkovich, Leeor
Shekhtman, Louis
Bazinet, Michel
Pântea, Victor
Placinta, Gheorge
Cotler, Scott J.
Vaillant, Andrew
Dahari, Harel
author_sort Hershkovich, Leeor
collection PubMed
description Analyzing the interplay among serum HBV DNA, HBsAg, anti-HBs, and alanine aminotransferase (ALT) during nucleic-acid polymer (NAP)-based therapy for chronic hepatitis B provides a unique opportunity to identify kinetic patterns associated with functional cure. METHODS: All participants with HBeAg-negative chronic HBV infection in the REP 401 study (NCT02565719) first received 24 weeks of tenofovir-disoproxil-fumarate (TDF) monotherapy. The early triple therapy group (n = 20) next received 48 weeks of TDF+pegylated interferon-α2a (pegIFN)+NAPs. In contrast, the delayed triple therapy group (n = 20) next received 24 weeks of TDF+pegIFN before 48 weeks of triple therapy. Three participants discontinued treatment and were excluded. Functional cure (HBsAg and HBV DNA not detectable with normal ALT) was assessed at 48 weeks post-treatment. Different kinetic phases were defined by at least a 2-fold change in slope. A single-phase decline was categorized as monophasic, and 2-phase declines were categorized as biphasic. RESULTS: Fourteen (35%) participants achieved a functional cure. HBV DNA remained below or near undetectable for all participants by the end of TDF monotherapy and during subsequent combination therapies. Three HBsAg kinetic patterns were found in both the early and delayed groups, nonresponders (n = 4 and n = 4), monophasic (n = 11 and n = 11), and biphasic (n = 4 and n = 3), respectively. All participants who achieved a functional cure had a monophasic HBsAg kinetic pattern during triple therapy. Among participants with a monophasic HBsAg decline, those who had a functional cure had a shorter median time to HBsAg loss of 21 (interquartile range=11) weeks compared with those who did not achieve functional cure [median: 27 (7) weeks] (p = 0.012). CONCLUSIONS: Functional cure was associated with a rapid monophasic HBsAg decline during NAP-based therapy. A nonmonophasic HBsAg kinetic pattern had a 100% negative predictive value (NPV) for a functional cure.
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spelling pubmed-103519422023-07-18 Rapid monophasic HBsAg decline during nucleic-acid polymer–based therapy predicts functional cure Hershkovich, Leeor Shekhtman, Louis Bazinet, Michel Pântea, Victor Placinta, Gheorge Cotler, Scott J. Vaillant, Andrew Dahari, Harel Hepatol Commun Original Article Analyzing the interplay among serum HBV DNA, HBsAg, anti-HBs, and alanine aminotransferase (ALT) during nucleic-acid polymer (NAP)-based therapy for chronic hepatitis B provides a unique opportunity to identify kinetic patterns associated with functional cure. METHODS: All participants with HBeAg-negative chronic HBV infection in the REP 401 study (NCT02565719) first received 24 weeks of tenofovir-disoproxil-fumarate (TDF) monotherapy. The early triple therapy group (n = 20) next received 48 weeks of TDF+pegylated interferon-α2a (pegIFN)+NAPs. In contrast, the delayed triple therapy group (n = 20) next received 24 weeks of TDF+pegIFN before 48 weeks of triple therapy. Three participants discontinued treatment and were excluded. Functional cure (HBsAg and HBV DNA not detectable with normal ALT) was assessed at 48 weeks post-treatment. Different kinetic phases were defined by at least a 2-fold change in slope. A single-phase decline was categorized as monophasic, and 2-phase declines were categorized as biphasic. RESULTS: Fourteen (35%) participants achieved a functional cure. HBV DNA remained below or near undetectable for all participants by the end of TDF monotherapy and during subsequent combination therapies. Three HBsAg kinetic patterns were found in both the early and delayed groups, nonresponders (n = 4 and n = 4), monophasic (n = 11 and n = 11), and biphasic (n = 4 and n = 3), respectively. All participants who achieved a functional cure had a monophasic HBsAg kinetic pattern during triple therapy. Among participants with a monophasic HBsAg decline, those who had a functional cure had a shorter median time to HBsAg loss of 21 (interquartile range=11) weeks compared with those who did not achieve functional cure [median: 27 (7) weeks] (p = 0.012). CONCLUSIONS: Functional cure was associated with a rapid monophasic HBsAg decline during NAP-based therapy. A nonmonophasic HBsAg kinetic pattern had a 100% negative predictive value (NPV) for a functional cure. Lippincott Williams & Wilkins 2023-07-17 /pmc/articles/PMC10351942/ /pubmed/37458583 http://dx.doi.org/10.1097/HC9.0000000000000205 Text en Copyright © 2023 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Association for the Study of Liver Diseases. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/)
spellingShingle Original Article
Hershkovich, Leeor
Shekhtman, Louis
Bazinet, Michel
Pântea, Victor
Placinta, Gheorge
Cotler, Scott J.
Vaillant, Andrew
Dahari, Harel
Rapid monophasic HBsAg decline during nucleic-acid polymer–based therapy predicts functional cure
title Rapid monophasic HBsAg decline during nucleic-acid polymer–based therapy predicts functional cure
title_full Rapid monophasic HBsAg decline during nucleic-acid polymer–based therapy predicts functional cure
title_fullStr Rapid monophasic HBsAg decline during nucleic-acid polymer–based therapy predicts functional cure
title_full_unstemmed Rapid monophasic HBsAg decline during nucleic-acid polymer–based therapy predicts functional cure
title_short Rapid monophasic HBsAg decline during nucleic-acid polymer–based therapy predicts functional cure
title_sort rapid monophasic hbsag decline during nucleic-acid polymer–based therapy predicts functional cure
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10351942/
https://www.ncbi.nlm.nih.gov/pubmed/37458583
http://dx.doi.org/10.1097/HC9.0000000000000205
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