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Adefovir Dipivoxil plus Chinese Medicine in HBeAg-Positive Chronic Hepatitis B Patients: A Randomized Controlled 48-Week Trial

Objective To evaluate the effects of a 48-week course of adefovir dipivoxil (ADV) plus Chinese medicine (CM) therapy, namely Tiaogan Jianpi Hexue (调肝健脾和血) and Tiaogan Jiedu Huashi (调肝解毒化湿) fomulae, in hepatitis B e antigen (HBeAg)-positive Chinese patients. Methods A total of 605 HBeAg-positive Chin...

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Published in:Chinese journal of integrative medicine 2020-05, Vol.26 (5), p.330-338
Main Authors: Li, Xiao-ke, Zhang, Ming-xiang, Shao, Feng-zhen, Zhou, Da-qiao, Xue, Jing-dong, Liu, Tie-jun, Chi, Xiao-ling, Lu, Bing-jiu, Wang, Xian-bo, Li, Qin, Li, Jun, Mao, De-wen, Yang, Hua-sheng, Yang, Hong-zhi, Zhao, Wen-xia, Li, Yong, Zhang, Guo-liang, Zhao, Yi-ming, Zou, Jian-dong, Liu, Meng-yang, Zhang, Ke-ke, Yang, Xian-zhao, Gan, Da-nan, Li, Ying, Zhang, Peng, Li, Zhi-guo, Li, Shuo, Ye, Yong-an
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Language:English
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Summary:Objective To evaluate the effects of a 48-week course of adefovir dipivoxil (ADV) plus Chinese medicine (CM) therapy, namely Tiaogan Jianpi Hexue (调肝健脾和血) and Tiaogan Jiedu Huashi (调肝解毒化湿) fomulae, in hepatitis B e antigen (HBeAg)-positive Chinese patients. Methods A total of 605 HBeAg-positive Chinese CHB patients were screened and 590 eligible participants were randomly assigned to 2 groups in 1:1 ratio including experimental group (EG, received ADV plus CM) and control group (CG, received ADV plus CM-placebo) for 48 weeks. The major study outcomes were the rates of HBeAg and HBV-DNA loss on week 12, 24, 36, 48, respectively. Secondary endpoints including liver functions (enzymes and bilirubin readings) were evaluated every 4 weeks at the beginning of week 24, 36, and 48. Routine blood, urine, and stool analyses in addition to electrocardiogram and abdominal B scan were monitored as safety evaluations. Adverse events (AEs) were documented. Results The combination therapy demonstrated superior HBeAg loss at 48 weeks, without additional AEs. The full analysis population was 560 and 280 in each group. In the EG, population achieved HBeAg loss on week 12, 24, 36, and 48 were 25 (8.90%), 34 (12.14%), 52 (18.57%), and 83 (29.64%), respectively; the equivalent numbers in the CG were 20 (7.14%), 41 (14.64%), 54 (19.29%), and 50 (17.86%), respectively. There was a statistically significant difference between these group values on week 48 (P
ISSN:1672-0415
1993-0402
DOI:10.1007/s11655-020-3250-0