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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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Vienna
2013
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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. |
format | Online Article Text |
id | pubmed-3888503 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Springer Vienna |
record_format | MEDLINE/PubMed |
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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