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240‐week entecavir maleate treatment in Chinese chronic hepatitis B predominantly genotype B or C

This study aimed to evaluate the efficacy and safety of entecavir(ETV) versus ETV maleate in Chinese patients with chronic hepatitis B(CHB). This was a randomized, double‐blind, double‐dummy, controlled, multicentre study. Patients were randomly assigned to receive 48 weeks of treatment with 0.5 mg/...

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Autores principales: Xu, Jing‐Hang, Fan, Ya‐Nan, Yu, Yan‐Yan, Si, Chong‐Wen, Zeng, Zheng, Xu, Zhong‐Nan, Li, Jun, Mao, Qing, Zhang, Da‐Zhi, Tang, Hong, Sheng, Ji‐Fang, Chen, Xin‐Yue, Ning, Qin, Shi, Guang‐Feng, Xie, Qing, Zhang, Xi‐Quan, Dai, Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9545224/
https://www.ncbi.nlm.nih.gov/pubmed/35737855
http://dx.doi.org/10.1111/jvh.13724
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author Xu, Jing‐Hang
Fan, Ya‐Nan
Yu, Yan‐Yan
Si, Chong‐Wen
Zeng, Zheng
Xu, Zhong‐Nan
Li, Jun
Mao, Qing
Zhang, Da‐Zhi
Tang, Hong
Sheng, Ji‐Fang
Chen, Xin‐Yue
Ning, Qin
Shi, Guang‐Feng
Xie, Qing
Zhang, Xi‐Quan
Dai, Jun
author_facet Xu, Jing‐Hang
Fan, Ya‐Nan
Yu, Yan‐Yan
Si, Chong‐Wen
Zeng, Zheng
Xu, Zhong‐Nan
Li, Jun
Mao, Qing
Zhang, Da‐Zhi
Tang, Hong
Sheng, Ji‐Fang
Chen, Xin‐Yue
Ning, Qin
Shi, Guang‐Feng
Xie, Qing
Zhang, Xi‐Quan
Dai, Jun
author_sort Xu, Jing‐Hang
collection PubMed
description This study aimed to evaluate the efficacy and safety of entecavir(ETV) versus ETV maleate in Chinese patients with chronic hepatitis B(CHB). This was a randomized, double‐blind, double‐dummy, controlled, multicentre study. Patients were randomly assigned to receive 48 weeks of treatment with 0.5 mg/day ETV (group A) or 0.5 mg/day ETV maleate (group B), then, all patients received treatment with 0.5 mg/day ETV maleate from week 49 onwards. Patients were regularly followed up. Serum hepatitis B virus (HBV) markers were detected. Adverse events (AE) were recorded. The primary endpoint was the decline in HBV DNA in each group at the end of treatment. Secondary endpoints included the rate of HBV DNA below the lower limit of detection (LLOD) (20 I U/ml) at the end of treatment, the rate of hepatitis B e antigen (HBeAg) loss, the rate of HBeAg seroconversion and serum alanine aminotransferase (ALT) normalization. One hundred and thirty‐seven (71 in group A) patients with HBeAg‐positive CHB and 46 (21 in group A) patients with HBeAg‐negative CHB completed the 240‐week treatment and follow‐up. Baseline characteristics were well balanced between the two groups. For the HBeAg‐positive CHB patients, the mean HBV DNA level had similarly decreased from baseline in both groups (A: by 6.67 log(10) IU/ml vs. B: by 6.74 log(10) IU/ml; p > .05) at Week 240. Patients who achieved undetectable levels of serum HBV DNA (<20 IU/ml) at Week 240 were similar between groups (A:91.55% vs. B:87.88%; p > .05). Both groups achieved similar HBeAg seroconversion rates at week 240 (A:26.98% vs. B:20.97%; p > .05). Both groups achieved similar normalization of ALT (A:87.32% vs. B:83.61%; p > .05) at Week 240 (p > .05). For the HBeAg‐negative CHB patients, the mean HBV DNA level had similarly decreased from baseline in both groups (A: by 6.05 log(10) IU/ml vs. B: by 6.10 log(10) IU/ml; p > .05) at Week 240. Patients who achieved undetectable levels of serum HBV DNA at Week 240 were similar between groups (A:100% vs. B:100%). Both groups achieved similar normalization rates (A:90.91% vs. B: 95.45%; p > .05) of ALT at Week 240 (p > .05). In conclusion, long‐term ETV maleate treatment was safe and efficient in Chinese CHB predominantly of genotype B or C.
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spelling pubmed-95452242022-10-14 240‐week entecavir maleate treatment in Chinese chronic hepatitis B predominantly genotype B or C Xu, Jing‐Hang Fan, Ya‐Nan Yu, Yan‐Yan Si, Chong‐Wen Zeng, Zheng Xu, Zhong‐Nan Li, Jun Mao, Qing Zhang, Da‐Zhi Tang, Hong Sheng, Ji‐Fang Chen, Xin‐Yue Ning, Qin Shi, Guang‐Feng Xie, Qing Zhang, Xi‐Quan Dai, Jun J Viral Hepat Original Articles This study aimed to evaluate the efficacy and safety of entecavir(ETV) versus ETV maleate in Chinese patients with chronic hepatitis B(CHB). This was a randomized, double‐blind, double‐dummy, controlled, multicentre study. Patients were randomly assigned to receive 48 weeks of treatment with 0.5 mg/day ETV (group A) or 0.5 mg/day ETV maleate (group B), then, all patients received treatment with 0.5 mg/day ETV maleate from week 49 onwards. Patients were regularly followed up. Serum hepatitis B virus (HBV) markers were detected. Adverse events (AE) were recorded. The primary endpoint was the decline in HBV DNA in each group at the end of treatment. Secondary endpoints included the rate of HBV DNA below the lower limit of detection (LLOD) (20 I U/ml) at the end of treatment, the rate of hepatitis B e antigen (HBeAg) loss, the rate of HBeAg seroconversion and serum alanine aminotransferase (ALT) normalization. One hundred and thirty‐seven (71 in group A) patients with HBeAg‐positive CHB and 46 (21 in group A) patients with HBeAg‐negative CHB completed the 240‐week treatment and follow‐up. Baseline characteristics were well balanced between the two groups. For the HBeAg‐positive CHB patients, the mean HBV DNA level had similarly decreased from baseline in both groups (A: by 6.67 log(10) IU/ml vs. B: by 6.74 log(10) IU/ml; p > .05) at Week 240. Patients who achieved undetectable levels of serum HBV DNA (<20 IU/ml) at Week 240 were similar between groups (A:91.55% vs. B:87.88%; p > .05). Both groups achieved similar HBeAg seroconversion rates at week 240 (A:26.98% vs. B:20.97%; p > .05). Both groups achieved similar normalization of ALT (A:87.32% vs. B:83.61%; p > .05) at Week 240 (p > .05). For the HBeAg‐negative CHB patients, the mean HBV DNA level had similarly decreased from baseline in both groups (A: by 6.05 log(10) IU/ml vs. B: by 6.10 log(10) IU/ml; p > .05) at Week 240. Patients who achieved undetectable levels of serum HBV DNA at Week 240 were similar between groups (A:100% vs. B:100%). Both groups achieved similar normalization rates (A:90.91% vs. B: 95.45%; p > .05) of ALT at Week 240 (p > .05). In conclusion, long‐term ETV maleate treatment was safe and efficient in Chinese CHB predominantly of genotype B or C. John Wiley and Sons Inc. 2022-07-06 2022-10 /pmc/articles/PMC9545224/ /pubmed/35737855 http://dx.doi.org/10.1111/jvh.13724 Text en © 2022 The Authors. Journal of Viral Hepatitis published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Xu, Jing‐Hang
Fan, Ya‐Nan
Yu, Yan‐Yan
Si, Chong‐Wen
Zeng, Zheng
Xu, Zhong‐Nan
Li, Jun
Mao, Qing
Zhang, Da‐Zhi
Tang, Hong
Sheng, Ji‐Fang
Chen, Xin‐Yue
Ning, Qin
Shi, Guang‐Feng
Xie, Qing
Zhang, Xi‐Quan
Dai, Jun
240‐week entecavir maleate treatment in Chinese chronic hepatitis B predominantly genotype B or C
title 240‐week entecavir maleate treatment in Chinese chronic hepatitis B predominantly genotype B or C
title_full 240‐week entecavir maleate treatment in Chinese chronic hepatitis B predominantly genotype B or C
title_fullStr 240‐week entecavir maleate treatment in Chinese chronic hepatitis B predominantly genotype B or C
title_full_unstemmed 240‐week entecavir maleate treatment in Chinese chronic hepatitis B predominantly genotype B or C
title_short 240‐week entecavir maleate treatment in Chinese chronic hepatitis B predominantly genotype B or C
title_sort 240‐week entecavir maleate treatment in chinese chronic hepatitis b predominantly genotype b or c
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9545224/
https://www.ncbi.nlm.nih.gov/pubmed/35737855
http://dx.doi.org/10.1111/jvh.13724
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