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Clinical characteristics of patients with chronic hepatitis B who developed genotypic resistance to entecavir: Real-life experience

BACKGROUND/AIMS: Clinical characteristics of patients with chronic hepatitis B (CHB) who developed genotypic resistance to entecavir (ETV) were compared to those without resistance. METHODS: Two hundred fifty eight CHB patients who underwent ETV treatment in our institution from July 2007 to May 201...

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Autores principales: Kim, Hong Joo, Cho, Yong Kyun, Jeon, Woo Kyu, Kim, Byung Ik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Association for the Study of the Liver 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5760008/
https://www.ncbi.nlm.nih.gov/pubmed/28870025
http://dx.doi.org/10.3350/cmh.2017.0005
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author Kim, Hong Joo
Cho, Yong Kyun
Jeon, Woo Kyu
Kim, Byung Ik
author_facet Kim, Hong Joo
Cho, Yong Kyun
Jeon, Woo Kyu
Kim, Byung Ik
author_sort Kim, Hong Joo
collection PubMed
description BACKGROUND/AIMS: Clinical characteristics of patients with chronic hepatitis B (CHB) who developed genotypic resistance to entecavir (ETV) were compared to those without resistance. METHODS: Two hundred fifty eight CHB patients who underwent ETV treatment in our institution from July 2007 to May 2013 were included. RESULTS: Eight (3.1%) patients developed genotypic resistance to ETV during the follow-up period. The patterns of genotypic resistance to ETV were as follows: L180M + M204V + S202G (n=3); M204I + V173M (n=1); I169V + V173M (n=1); L180M + M204V + V173L (n=1); L180M + M204V + V173L + M250V (n=1); M204I + V214A + P237H (n=1). The cumulative occurrence rates of genotypic resistance to ETV were not significantly different between CHB patients with prior nucleos(t)tide analogues (NA) exposure (NA experienced, n=56) and NA naïve patients (n=202, P=0.823 by log rank comparison). Older age, higher baseline log(10)hepatitis B virus-deoxynucleic acid (log(10)HBV-DNA), higher log(10)HBV-DNA at 3, 6, 12 and 24 months after baseline, and complete virologic response (CVR, undetectable serum HBV-DNA by polymerase chain reaction 6 months after ETV treatment) were significant contributors to the development of genotypic resistance to ETV. Multivariate analyses showed higher log(10)HBV-DNA 6 months after baseline and absence of CVR were independent and significant contributors to the development of ETV resistance. CONCLUSIONS: Clinical characteristics of patients who developed ETV resistance were higher log(10)HBV-DNA 6 months after baseline and absence of CVR during the ETV treatment.
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spelling pubmed-57600082018-01-12 Clinical characteristics of patients with chronic hepatitis B who developed genotypic resistance to entecavir: Real-life experience Kim, Hong Joo Cho, Yong Kyun Jeon, Woo Kyu Kim, Byung Ik Clin Mol Hepatol Original Article BACKGROUND/AIMS: Clinical characteristics of patients with chronic hepatitis B (CHB) who developed genotypic resistance to entecavir (ETV) were compared to those without resistance. METHODS: Two hundred fifty eight CHB patients who underwent ETV treatment in our institution from July 2007 to May 2013 were included. RESULTS: Eight (3.1%) patients developed genotypic resistance to ETV during the follow-up period. The patterns of genotypic resistance to ETV were as follows: L180M + M204V + S202G (n=3); M204I + V173M (n=1); I169V + V173M (n=1); L180M + M204V + V173L (n=1); L180M + M204V + V173L + M250V (n=1); M204I + V214A + P237H (n=1). The cumulative occurrence rates of genotypic resistance to ETV were not significantly different between CHB patients with prior nucleos(t)tide analogues (NA) exposure (NA experienced, n=56) and NA naïve patients (n=202, P=0.823 by log rank comparison). Older age, higher baseline log(10)hepatitis B virus-deoxynucleic acid (log(10)HBV-DNA), higher log(10)HBV-DNA at 3, 6, 12 and 24 months after baseline, and complete virologic response (CVR, undetectable serum HBV-DNA by polymerase chain reaction 6 months after ETV treatment) were significant contributors to the development of genotypic resistance to ETV. Multivariate analyses showed higher log(10)HBV-DNA 6 months after baseline and absence of CVR were independent and significant contributors to the development of ETV resistance. CONCLUSIONS: Clinical characteristics of patients who developed ETV resistance were higher log(10)HBV-DNA 6 months after baseline and absence of CVR during the ETV treatment. The Korean Association for the Study of the Liver 2017-12 2017-09-05 /pmc/articles/PMC5760008/ /pubmed/28870025 http://dx.doi.org/10.3350/cmh.2017.0005 Text en Copyright © 2017 by The Korean Association for the Study of the Liver This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Kim, Hong Joo
Cho, Yong Kyun
Jeon, Woo Kyu
Kim, Byung Ik
Clinical characteristics of patients with chronic hepatitis B who developed genotypic resistance to entecavir: Real-life experience
title Clinical characteristics of patients with chronic hepatitis B who developed genotypic resistance to entecavir: Real-life experience
title_full Clinical characteristics of patients with chronic hepatitis B who developed genotypic resistance to entecavir: Real-life experience
title_fullStr Clinical characteristics of patients with chronic hepatitis B who developed genotypic resistance to entecavir: Real-life experience
title_full_unstemmed Clinical characteristics of patients with chronic hepatitis B who developed genotypic resistance to entecavir: Real-life experience
title_short Clinical characteristics of patients with chronic hepatitis B who developed genotypic resistance to entecavir: Real-life experience
title_sort clinical characteristics of patients with chronic hepatitis b who developed genotypic resistance to entecavir: real-life experience
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5760008/
https://www.ncbi.nlm.nih.gov/pubmed/28870025
http://dx.doi.org/10.3350/cmh.2017.0005
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