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Peginterferon and Entecavir Combination Therapy Improves Outcome of Non–Early Response Hepatitis B e Antigen–Positive Patients
BACKGROUND: The efficacy of nucleot(s)ide analogs (NAs) and pegylated interferon (PegIFN) combination therapy for hepatitis B e antigen–positive (HBeAg(+)) patients is still controversial. Whether PegIFN and entecavir (ETV) combination therapy could provide a greater benefit for HBeAg(+) patients wa...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8050793/ https://www.ncbi.nlm.nih.gov/pubmed/33889654 http://dx.doi.org/10.1093/ofid/ofaa462 |
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author | Chen, Lu Lin, Lanyi Zhou, Huijuan Tang, Weiliang Wang, Hui Cai, Wei Bao, Shisan Guo, Simin Xie, Qing |
author_facet | Chen, Lu Lin, Lanyi Zhou, Huijuan Tang, Weiliang Wang, Hui Cai, Wei Bao, Shisan Guo, Simin Xie, Qing |
author_sort | Chen, Lu |
collection | PubMed |
description | BACKGROUND: The efficacy of nucleot(s)ide analogs (NAs) and pegylated interferon (PegIFN) combination therapy for hepatitis B e antigen–positive (HBeAg(+)) patients is still controversial. Whether PegIFN and entecavir (ETV) combination therapy could provide a greater benefit for HBeAg(+) patients was assessed. METHODS: Treatment-naïve HBeAg(+) patients initiated on PegIFN alfa-2a (PegIFNα-2a) for 24 weeks without early response (early response: HBsAg <1500 IU/mL and hepatitis B virus [HBV] DNA <10(5) copies/mL) were recruited in the current study. Among total of 94 patients, 51 were continued on PegIFNα-2a monotherapy, and 43 were offered PegIFNα-2a and ETV combined therapy. RESULTS: Better outcomes in response to the combined therapy, compared with that of the monotherapy, were demonstrated, including more HBsAg decline and loss and HBV DNA decline and HBeAg clearance. Importantly, the patients with HBsAg levels between 1500 and 20( )000 IU/mL initially or between 5000 and 20( )000 IU/mL after 24 weeks of PegIFNα-2a benefitted more from the combined therapy, compared with those on monotherapy. CONCLUSIONS: Combined therapy of PegIFNα-2a and ETV is more efficacious for HBeAg(+) patients without early response to PegIFN monotherapy, and HBsAg levels are a good predictor of treatment outcomes. |
format | Online Article Text |
id | pubmed-8050793 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-80507932021-04-21 Peginterferon and Entecavir Combination Therapy Improves Outcome of Non–Early Response Hepatitis B e Antigen–Positive Patients Chen, Lu Lin, Lanyi Zhou, Huijuan Tang, Weiliang Wang, Hui Cai, Wei Bao, Shisan Guo, Simin Xie, Qing Open Forum Infect Dis Major Articles BACKGROUND: The efficacy of nucleot(s)ide analogs (NAs) and pegylated interferon (PegIFN) combination therapy for hepatitis B e antigen–positive (HBeAg(+)) patients is still controversial. Whether PegIFN and entecavir (ETV) combination therapy could provide a greater benefit for HBeAg(+) patients was assessed. METHODS: Treatment-naïve HBeAg(+) patients initiated on PegIFN alfa-2a (PegIFNα-2a) for 24 weeks without early response (early response: HBsAg <1500 IU/mL and hepatitis B virus [HBV] DNA <10(5) copies/mL) were recruited in the current study. Among total of 94 patients, 51 were continued on PegIFNα-2a monotherapy, and 43 were offered PegIFNα-2a and ETV combined therapy. RESULTS: Better outcomes in response to the combined therapy, compared with that of the monotherapy, were demonstrated, including more HBsAg decline and loss and HBV DNA decline and HBeAg clearance. Importantly, the patients with HBsAg levels between 1500 and 20( )000 IU/mL initially or between 5000 and 20( )000 IU/mL after 24 weeks of PegIFNα-2a benefitted more from the combined therapy, compared with those on monotherapy. CONCLUSIONS: Combined therapy of PegIFNα-2a and ETV is more efficacious for HBeAg(+) patients without early response to PegIFN monotherapy, and HBsAg levels are a good predictor of treatment outcomes. Oxford University Press 2020-09-30 /pmc/articles/PMC8050793/ /pubmed/33889654 http://dx.doi.org/10.1093/ofid/ofaa462 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of Infectious Diseases Society of America. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Major Articles Chen, Lu Lin, Lanyi Zhou, Huijuan Tang, Weiliang Wang, Hui Cai, Wei Bao, Shisan Guo, Simin Xie, Qing Peginterferon and Entecavir Combination Therapy Improves Outcome of Non–Early Response Hepatitis B e Antigen–Positive Patients |
title | Peginterferon and Entecavir Combination Therapy Improves Outcome of Non–Early Response Hepatitis B e Antigen–Positive Patients |
title_full | Peginterferon and Entecavir Combination Therapy Improves Outcome of Non–Early Response Hepatitis B e Antigen–Positive Patients |
title_fullStr | Peginterferon and Entecavir Combination Therapy Improves Outcome of Non–Early Response Hepatitis B e Antigen–Positive Patients |
title_full_unstemmed | Peginterferon and Entecavir Combination Therapy Improves Outcome of Non–Early Response Hepatitis B e Antigen–Positive Patients |
title_short | Peginterferon and Entecavir Combination Therapy Improves Outcome of Non–Early Response Hepatitis B e Antigen–Positive Patients |
title_sort | peginterferon and entecavir combination therapy improves outcome of non–early response hepatitis b e antigen–positive patients |
topic | Major Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8050793/ https://www.ncbi.nlm.nih.gov/pubmed/33889654 http://dx.doi.org/10.1093/ofid/ofaa462 |
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