Cargando…

The efficacy of pegylated interferon alpha-2a and entecavir in HBeAg-positive children and adolescents with chronic hepatitis B

BACKGROUND AND OBJECTIVES: Pegylated interferon alpha-2a (peg-IFN α-2a) and entecavir (ETV) are both recommended as the first-line antiviral drugs for chronic hepatitis B (CHB) at present. We aimed to compare the efficacy and safety between peg-IFN α-2a and ETV initial therapy in children and adoles...

Descripción completa

Detalles Bibliográficos
Autores principales: He, Yi, Zhou, Yingzhi, Wang, Huimin, Peng, Xiaorong, Chang, Yunan, Hu, Peng, Ren, Hong, Xu, Hongmei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9297582/
https://www.ncbi.nlm.nih.gov/pubmed/35854256
http://dx.doi.org/10.1186/s12887-022-03482-0
_version_ 1784750504716271616
author He, Yi
Zhou, Yingzhi
Wang, Huimin
Peng, Xiaorong
Chang, Yunan
Hu, Peng
Ren, Hong
Xu, Hongmei
author_facet He, Yi
Zhou, Yingzhi
Wang, Huimin
Peng, Xiaorong
Chang, Yunan
Hu, Peng
Ren, Hong
Xu, Hongmei
author_sort He, Yi
collection PubMed
description BACKGROUND AND OBJECTIVES: Pegylated interferon alpha-2a (peg-IFN α-2a) and entecavir (ETV) are both recommended as the first-line antiviral drugs for chronic hepatitis B (CHB) at present. We aimed to compare the efficacy and safety between peg-IFN α-2a and ETV initial therapy in children and adolescents with CHB and investigate the potential factors affecting the treatment response during the first 48 weeks. METHODS: We retrospectively selected 70 treatment-naïve children and adolescents with CHB who received peg-IFN α-2a(n = 26) or ETV(n = 44) as initial therapy and completed 48-week follow-up for data analysis. Blood samples before treatment were collected from 26 patients of the cohort to assess the cytokine profiles. RESULTS: We found that initial peg-IFN therapy results in higher rates of hepatitis B surface antigen (HBsAg) serological response (SR) but lower rates of virological and biochemical response rates compared to ETV at week 48. As for achieving hepatitis B e antigen (HBeAg) SR, peg-IFN was comparable to ETV in the univariate analysis and turned out to be better than ETV after adjustment for important baseline factors. We also found that elevated pre-treatment IL-18 level was significantly associated with HBeAg SR, and remained as the only independent factor of predicting HBeAg SR after adjustment for other important factors. No serious adverse effects of the 2 drugs were reported during the 48-week follow-up. CONCLUSIONS: comparing to ETV, peg-IFN was superior in achieving HBsAg and HBeAg SR; higher baseline IL-18 levels were independently associated with HBeAg SR in this study of children and adolescents with CHB. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12887-022-03482-0.
format Online
Article
Text
id pubmed-9297582
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-92975822022-07-21 The efficacy of pegylated interferon alpha-2a and entecavir in HBeAg-positive children and adolescents with chronic hepatitis B He, Yi Zhou, Yingzhi Wang, Huimin Peng, Xiaorong Chang, Yunan Hu, Peng Ren, Hong Xu, Hongmei BMC Pediatr Research BACKGROUND AND OBJECTIVES: Pegylated interferon alpha-2a (peg-IFN α-2a) and entecavir (ETV) are both recommended as the first-line antiviral drugs for chronic hepatitis B (CHB) at present. We aimed to compare the efficacy and safety between peg-IFN α-2a and ETV initial therapy in children and adolescents with CHB and investigate the potential factors affecting the treatment response during the first 48 weeks. METHODS: We retrospectively selected 70 treatment-naïve children and adolescents with CHB who received peg-IFN α-2a(n = 26) or ETV(n = 44) as initial therapy and completed 48-week follow-up for data analysis. Blood samples before treatment were collected from 26 patients of the cohort to assess the cytokine profiles. RESULTS: We found that initial peg-IFN therapy results in higher rates of hepatitis B surface antigen (HBsAg) serological response (SR) but lower rates of virological and biochemical response rates compared to ETV at week 48. As for achieving hepatitis B e antigen (HBeAg) SR, peg-IFN was comparable to ETV in the univariate analysis and turned out to be better than ETV after adjustment for important baseline factors. We also found that elevated pre-treatment IL-18 level was significantly associated with HBeAg SR, and remained as the only independent factor of predicting HBeAg SR after adjustment for other important factors. No serious adverse effects of the 2 drugs were reported during the 48-week follow-up. CONCLUSIONS: comparing to ETV, peg-IFN was superior in achieving HBsAg and HBeAg SR; higher baseline IL-18 levels were independently associated with HBeAg SR in this study of children and adolescents with CHB. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12887-022-03482-0. BioMed Central 2022-07-20 /pmc/articles/PMC9297582/ /pubmed/35854256 http://dx.doi.org/10.1186/s12887-022-03482-0 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
He, Yi
Zhou, Yingzhi
Wang, Huimin
Peng, Xiaorong
Chang, Yunan
Hu, Peng
Ren, Hong
Xu, Hongmei
The efficacy of pegylated interferon alpha-2a and entecavir in HBeAg-positive children and adolescents with chronic hepatitis B
title The efficacy of pegylated interferon alpha-2a and entecavir in HBeAg-positive children and adolescents with chronic hepatitis B
title_full The efficacy of pegylated interferon alpha-2a and entecavir in HBeAg-positive children and adolescents with chronic hepatitis B
title_fullStr The efficacy of pegylated interferon alpha-2a and entecavir in HBeAg-positive children and adolescents with chronic hepatitis B
title_full_unstemmed The efficacy of pegylated interferon alpha-2a and entecavir in HBeAg-positive children and adolescents with chronic hepatitis B
title_short The efficacy of pegylated interferon alpha-2a and entecavir in HBeAg-positive children and adolescents with chronic hepatitis B
title_sort efficacy of pegylated interferon alpha-2a and entecavir in hbeag-positive children and adolescents with chronic hepatitis b
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9297582/
https://www.ncbi.nlm.nih.gov/pubmed/35854256
http://dx.doi.org/10.1186/s12887-022-03482-0
work_keys_str_mv AT heyi theefficacyofpegylatedinterferonalpha2aandentecavirinhbeagpositivechildrenandadolescentswithchronichepatitisb
AT zhouyingzhi theefficacyofpegylatedinterferonalpha2aandentecavirinhbeagpositivechildrenandadolescentswithchronichepatitisb
AT wanghuimin theefficacyofpegylatedinterferonalpha2aandentecavirinhbeagpositivechildrenandadolescentswithchronichepatitisb
AT pengxiaorong theefficacyofpegylatedinterferonalpha2aandentecavirinhbeagpositivechildrenandadolescentswithchronichepatitisb
AT changyunan theefficacyofpegylatedinterferonalpha2aandentecavirinhbeagpositivechildrenandadolescentswithchronichepatitisb
AT hupeng theefficacyofpegylatedinterferonalpha2aandentecavirinhbeagpositivechildrenandadolescentswithchronichepatitisb
AT renhong theefficacyofpegylatedinterferonalpha2aandentecavirinhbeagpositivechildrenandadolescentswithchronichepatitisb
AT xuhongmei theefficacyofpegylatedinterferonalpha2aandentecavirinhbeagpositivechildrenandadolescentswithchronichepatitisb
AT heyi efficacyofpegylatedinterferonalpha2aandentecavirinhbeagpositivechildrenandadolescentswithchronichepatitisb
AT zhouyingzhi efficacyofpegylatedinterferonalpha2aandentecavirinhbeagpositivechildrenandadolescentswithchronichepatitisb
AT wanghuimin efficacyofpegylatedinterferonalpha2aandentecavirinhbeagpositivechildrenandadolescentswithchronichepatitisb
AT pengxiaorong efficacyofpegylatedinterferonalpha2aandentecavirinhbeagpositivechildrenandadolescentswithchronichepatitisb
AT changyunan efficacyofpegylatedinterferonalpha2aandentecavirinhbeagpositivechildrenandadolescentswithchronichepatitisb
AT hupeng efficacyofpegylatedinterferonalpha2aandentecavirinhbeagpositivechildrenandadolescentswithchronichepatitisb
AT renhong efficacyofpegylatedinterferonalpha2aandentecavirinhbeagpositivechildrenandadolescentswithchronichepatitisb
AT xuhongmei efficacyofpegylatedinterferonalpha2aandentecavirinhbeagpositivechildrenandadolescentswithchronichepatitisb