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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.
Afiliação
  • Xu JH; Department of Infectious Diseases, Center for Liver Diseases, Peking University First Hospital, Beijing, China.
  • Fan YN; Department of Infectious Diseases, Center for Liver Diseases, Peking University First Hospital, Beijing, China.
  • Yu YY; Department of Infectious Diseases, Center for Liver Diseases, Peking University First Hospital, Beijing, China.
  • Si CW; Department of Infectious Diseases, Center for Liver Diseases, Peking University First Hospital, Beijing, China.
  • Zeng Z; Department of Infectious Diseases, Center for Liver Diseases, Peking University First Hospital, Beijing, China.
  • Xu ZN; Jiangsu Chia-tai Tianqing Pharmaceutical Co, Ltd, Nanjing, China.
  • Li J; Department of Infectious Diseases, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
  • Mao Q; Department of Infectious Diseases, Southwest China Hospital, Chongqing, China.
  • Zhang DZ; Department of Infectious Diseases, The Second Affiliated Hospital of Chongqing Medical University, Chongqing, China.
  • Tang H; Department of Infectious Diseases, West China Hospital, Chengdu, China.
  • Sheng JF; Department of Infectious Diseases, The First Affiliated Hospital of Zhejiang University, Hangzhou, China.
  • Chen XY; Department of International Medicine, Beijing Youan Hospital, Capital Medical University, Beijing, China.
  • Ning Q; Department and Institute of Infectious Diseases, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
  • Shi GF; Department of Infectious Diseases, Huashan Hospital, Fudan University, Shanghai, China.
  • Xie Q; Department of Infectious Diseases, Ruijin Hospital, Jiaotong University School of Medicine, Shanghai, China.
  • Zhang XQ; Jiangsu Chia-tai Tianqing Pharmaceutical Co, Ltd, Nanjing, China.
  • Dai J; Jiangsu Chia-tai Tianqing Pharmaceutical Co, Ltd, Nanjing, China.
J Viral Hepat ; 29(10): 862-867, 2022 Oct.
Article em En | MEDLINE | ID: mdl-35737855
ABSTRACT
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 log10 IU/ml vs. B by 6.74 log10 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 (A91.55% vs. B87.88%; p > .05). Both groups achieved similar HBeAg seroconversion rates at week 240 (A26.98% vs. B20.97%; p > .05). Both groups achieved similar normalization of ALT (A87.32% vs. B83.61%; 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 log10 IU/ml vs. B by 6.10 log10 IU/ml; p > .05) at Week 240. Patients who achieved undetectable levels of serum HBV DNA at Week 240 were similar between groups (A100% vs. B100%). Both groups achieved similar normalization rates (A90.91% 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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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Hepatite B Crônica Tipo de estudo: Clinical_trials Limite: Humans País/Região como assunto: Asia Idioma: En Revista: J Viral Hepat Assunto da revista: GASTROENTEROLOGIA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Hepatite B Crônica Tipo de estudo: Clinical_trials Limite: Humans País/Região como assunto: Asia Idioma: En Revista: J Viral Hepat Assunto da revista: GASTROENTEROLOGIA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: China