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Long-term virological outcome in chronic hepatitis B patients with a partial virological response to entecavir

BACKGROUND/AIMS: The clinical outcome of patients with a partial virological response (PVR) to entecavir (ETV), in particular nucloes(t)ide analogue (NA)-experienced patients, has not been thoroughly investigated. The aim of the present study was to assess long-term outcomes in NA-naive and NA-exper...

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Autores principales: Jo, Yu Jung, Kim, Kyung-Ah, Lee, June Sung, Kim, Nam-Hoon, Bae, Won Ki, Song, Tae June, Kim, Jeong Wook
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Association of Internal Medicine 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4351323/
https://www.ncbi.nlm.nih.gov/pubmed/25750558
http://dx.doi.org/10.3904/kjim.2015.30.2.170
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author Jo, Yu Jung
Kim, Kyung-Ah
Lee, June Sung
Kim, Nam-Hoon
Bae, Won Ki
Song, Tae June
Kim, Jeong Wook
author_facet Jo, Yu Jung
Kim, Kyung-Ah
Lee, June Sung
Kim, Nam-Hoon
Bae, Won Ki
Song, Tae June
Kim, Jeong Wook
author_sort Jo, Yu Jung
collection PubMed
description BACKGROUND/AIMS: The clinical outcome of patients with a partial virological response (PVR) to entecavir (ETV), in particular nucloes(t)ide analogue (NA)-experienced patients, has not been thoroughly investigated. The aim of the present study was to assess long-term outcomes in NA-naive and NA-experienced chronic hepatitis B patients with a PVR to ETV. METHODS: Chronic hepatitis B patients treated with ETV (0.5 mg/day) for at least 1 year were enrolled retrospectively. PVR was defined as a decrease in hepatitis B virus (HBV) DNA titer of more than 2 log(10) IU/mL, yet with residual serum HBV DNA, as determined by real time-polymerase chain reaction, at week 48 of ETV therapy. RESULTS: A total of 202 patients (127 NA-naive and 75 NA-experienced, male 70.8%, antigen positive 53.2%, baseline serum HBV DNA 6.2 ± 1.5 log(10) IU/mL) were analyzed. Twenty-eight patients demonstrated a PVR. The PVR was associated with a high serum HBV DNA titer at baseline and at week 24. Virological response (< 60 IU/mL) was achieved in 46.2%, 61.5%, 77.6%, and 85% of patients with PVR at week 72, 96, 144, and 192, respectively. Resistance to antivirals developed in two NA-experienced patients. Failure of virological response (VR) in patients with PVR was associated with high levels of serum HBV DNA at week 48. CONCLUSIONS: Patients with PVR to ETV had favorable long-term virological outcomes. The low serum level of HBV DNA (< 200 IU/mL) at week 48 was associated with subsequent development of a VR in patients with PVR to ETV.
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spelling pubmed-43513232015-03-06 Long-term virological outcome in chronic hepatitis B patients with a partial virological response to entecavir Jo, Yu Jung Kim, Kyung-Ah Lee, June Sung Kim, Nam-Hoon Bae, Won Ki Song, Tae June Kim, Jeong Wook Korean J Intern Med Original Article BACKGROUND/AIMS: The clinical outcome of patients with a partial virological response (PVR) to entecavir (ETV), in particular nucloes(t)ide analogue (NA)-experienced patients, has not been thoroughly investigated. The aim of the present study was to assess long-term outcomes in NA-naive and NA-experienced chronic hepatitis B patients with a PVR to ETV. METHODS: Chronic hepatitis B patients treated with ETV (0.5 mg/day) for at least 1 year were enrolled retrospectively. PVR was defined as a decrease in hepatitis B virus (HBV) DNA titer of more than 2 log(10) IU/mL, yet with residual serum HBV DNA, as determined by real time-polymerase chain reaction, at week 48 of ETV therapy. RESULTS: A total of 202 patients (127 NA-naive and 75 NA-experienced, male 70.8%, antigen positive 53.2%, baseline serum HBV DNA 6.2 ± 1.5 log(10) IU/mL) were analyzed. Twenty-eight patients demonstrated a PVR. The PVR was associated with a high serum HBV DNA titer at baseline and at week 24. Virological response (< 60 IU/mL) was achieved in 46.2%, 61.5%, 77.6%, and 85% of patients with PVR at week 72, 96, 144, and 192, respectively. Resistance to antivirals developed in two NA-experienced patients. Failure of virological response (VR) in patients with PVR was associated with high levels of serum HBV DNA at week 48. CONCLUSIONS: Patients with PVR to ETV had favorable long-term virological outcomes. The low serum level of HBV DNA (< 200 IU/mL) at week 48 was associated with subsequent development of a VR in patients with PVR to ETV. The Korean Association of Internal Medicine 2015-03 2015-02-27 /pmc/articles/PMC4351323/ /pubmed/25750558 http://dx.doi.org/10.3904/kjim.2015.30.2.170 Text en Copyright © 2015 The Korean Association of Internal Medicine http://creativecommons.org/licenses/by-nc/3.0/ 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
Jo, Yu Jung
Kim, Kyung-Ah
Lee, June Sung
Kim, Nam-Hoon
Bae, Won Ki
Song, Tae June
Kim, Jeong Wook
Long-term virological outcome in chronic hepatitis B patients with a partial virological response to entecavir
title Long-term virological outcome in chronic hepatitis B patients with a partial virological response to entecavir
title_full Long-term virological outcome in chronic hepatitis B patients with a partial virological response to entecavir
title_fullStr Long-term virological outcome in chronic hepatitis B patients with a partial virological response to entecavir
title_full_unstemmed Long-term virological outcome in chronic hepatitis B patients with a partial virological response to entecavir
title_short Long-term virological outcome in chronic hepatitis B patients with a partial virological response to entecavir
title_sort long-term virological outcome in chronic hepatitis b patients with a partial virological response to entecavir
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4351323/
https://www.ncbi.nlm.nih.gov/pubmed/25750558
http://dx.doi.org/10.3904/kjim.2015.30.2.170
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