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Telbivudine and adefovir combination therapy for patients with chronic lamivudine-resistant hepatitis B virus infections

We evaluated second-line salvage therapy with adefovir + telbivudine (group 1), adefovir followed by adefovir + telbivudine (group 2), or lamivudine + adefovir followed by adefovir + telbivudine (group 3) in hepatitis B patients with an inadequate virologic response to lamivudine treatment. Simple l...

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Autores principales: Lin, Ming-Tsung, Chou, Yeh-Pin, Hu, Tsung-Hui, Yu, Hsien-Chung, Hsu, Yu-Chun, Tsai, Ming-Chao, Tseng, Po-Lin, Chang, Kuo-Chin, Yen, Yi-Hao, Chiu, King-Wah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Vienna 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3888503/
https://www.ncbi.nlm.nih.gov/pubmed/23857507
http://dx.doi.org/10.1007/s00705-013-1786-4
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author Lin, Ming-Tsung
Chou, Yeh-Pin
Hu, Tsung-Hui
Yu, Hsien-Chung
Hsu, Yu-Chun
Tsai, Ming-Chao
Tseng, Po-Lin
Chang, Kuo-Chin
Yen, Yi-Hao
Chiu, King-Wah
author_facet Lin, Ming-Tsung
Chou, Yeh-Pin
Hu, Tsung-Hui
Yu, Hsien-Chung
Hsu, Yu-Chun
Tsai, Ming-Chao
Tseng, Po-Lin
Chang, Kuo-Chin
Yen, Yi-Hao
Chiu, King-Wah
author_sort Lin, Ming-Tsung
collection PubMed
description We evaluated second-line salvage therapy with adefovir + telbivudine (group 1), adefovir followed by adefovir + telbivudine (group 2), or lamivudine + adefovir followed by adefovir + telbivudine (group 3) in hepatitis B patients with an inadequate virologic response to lamivudine treatment. Simple linear regression analysis showed that for each additional month of treatment, the most significant reduction in viral load occurred in group 1 (HBV DNA [Log(10) IU/mL]: group 1, −0.149; group 2, -0.081; group 3, −0.123). Generalized estimating equation analysis revealed that compared to group 1, hepatitis B virus (HBV) DNA levels were 1.203 and 0.443 Log(10) IU/mL higher in groups 2 and 3, respectively. Overall, a significant reduction in viral load (−0.060 Log(10) IU/mL) was observed for each additional month of treatment. Adefovir + telbivudine treatment resulted in a significant reduction in HBV DNA levels. Moreover, telbivudine treatment resulted in a significant reduction in viral load (−0.050 Log(10) IU/mL) compared to lamivudine treatment after the emergence of lamivudine resistance. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00705-013-1786-4) contains supplementary material, which is available to authorized users.
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spelling pubmed-38885032014-01-14 Telbivudine and adefovir combination therapy for patients with chronic lamivudine-resistant hepatitis B virus infections Lin, Ming-Tsung Chou, Yeh-Pin Hu, Tsung-Hui Yu, Hsien-Chung Hsu, Yu-Chun Tsai, Ming-Chao Tseng, Po-Lin Chang, Kuo-Chin Yen, Yi-Hao Chiu, King-Wah Arch Virol Original Article We evaluated second-line salvage therapy with adefovir + telbivudine (group 1), adefovir followed by adefovir + telbivudine (group 2), or lamivudine + adefovir followed by adefovir + telbivudine (group 3) in hepatitis B patients with an inadequate virologic response to lamivudine treatment. Simple linear regression analysis showed that for each additional month of treatment, the most significant reduction in viral load occurred in group 1 (HBV DNA [Log(10) IU/mL]: group 1, −0.149; group 2, -0.081; group 3, −0.123). Generalized estimating equation analysis revealed that compared to group 1, hepatitis B virus (HBV) DNA levels were 1.203 and 0.443 Log(10) IU/mL higher in groups 2 and 3, respectively. Overall, a significant reduction in viral load (−0.060 Log(10) IU/mL) was observed for each additional month of treatment. Adefovir + telbivudine treatment resulted in a significant reduction in HBV DNA levels. Moreover, telbivudine treatment resulted in a significant reduction in viral load (−0.050 Log(10) IU/mL) compared to lamivudine treatment after the emergence of lamivudine resistance. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00705-013-1786-4) contains supplementary material, which is available to authorized users. Springer Vienna 2013-07-16 2014 /pmc/articles/PMC3888503/ /pubmed/23857507 http://dx.doi.org/10.1007/s00705-013-1786-4 Text en © The Author(s) 2013 https://creativecommons.org/licenses/by/2.0/ Open AccessThis article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Original Article
Lin, Ming-Tsung
Chou, Yeh-Pin
Hu, Tsung-Hui
Yu, Hsien-Chung
Hsu, Yu-Chun
Tsai, Ming-Chao
Tseng, Po-Lin
Chang, Kuo-Chin
Yen, Yi-Hao
Chiu, King-Wah
Telbivudine and adefovir combination therapy for patients with chronic lamivudine-resistant hepatitis B virus infections
title Telbivudine and adefovir combination therapy for patients with chronic lamivudine-resistant hepatitis B virus infections
title_full Telbivudine and adefovir combination therapy for patients with chronic lamivudine-resistant hepatitis B virus infections
title_fullStr Telbivudine and adefovir combination therapy for patients with chronic lamivudine-resistant hepatitis B virus infections
title_full_unstemmed Telbivudine and adefovir combination therapy for patients with chronic lamivudine-resistant hepatitis B virus infections
title_short Telbivudine and adefovir combination therapy for patients with chronic lamivudine-resistant hepatitis B virus infections
title_sort telbivudine and adefovir combination therapy for patients with chronic lamivudine-resistant hepatitis b virus infections
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3888503/
https://www.ncbi.nlm.nih.gov/pubmed/23857507
http://dx.doi.org/10.1007/s00705-013-1786-4
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