Zhang Jing-Hao, Zhang Xin, Zhou Zhen-Hua, Zhu Xiao-Jun, Zheng Chao, Li Man, Jin Shu-Gen, Mao De-Wen, Xue Jing-Dong, Shi Wei-Bing, Chi Xiao-Ling, Wang Xian-Bo, Li Xiao-Dong, Li Yong, Wang Hui, Li Qin, Zhou Da-Qiao, Wang Cheng-Bao, Shi Chang-He, Li Cheng-Zhong, Wu Jian-Hua, Kong Xiao-Ni, Sun Xue-Hua, Gao Yue-Qiu
Department of Hepatopathy, Shuguang Hospital, Affiliated to Shanghai University of Traditional Chinese Medicine, Shanghai 201203, China.
Laboratory of Cellular Immunity, Shanghai Key Laboratory of Traditional Chinese Medicine, Affiliated to Shanghai University of Traditional Chinese Medicine, Shanghai 201203, China.
Evid Based Complement Alternat Med. 2022 Mar 25;2022:6097221. doi: 10.1155/2022/6097221. eCollection 2022.
Bushen Jianpi formula (BSJPF, also known as Lingmao formula) is a traditional Chinese medicine for chronic hepatitis B (CHB). The previous study has suggested that the treatment combination of BSJPF and entecavir (ETV) can achieve a significant loss of hepatitis B e antigen (HBeAg) and a significant decrease in serum level of hepatitis B virus (HBV) DNA in HBeAg-positive CHB patients with mildly elevated alanine aminotransferase.
This study aimed to evaluate the efficacy and safety of BSJPF combined with ETV for treating HBeAg-negative CHB patients.
A total of 640 patients were assigned randomly to the treatment group (receiving BSJPF combined with ETV for 96 weeks) or the control group (receiving a placebo combined with ETV for 96 weeks) in a 1 : 1 ratio. The primary endpoints are the rate of loss of hepatitis B surface antigen (HBsAg). The secondary outcomes included the rate of decrease in the HBsAg concentration to ≥1 lg·IU/mL, the HBV DNA suppression, the decline of the level of covalently closed circular DNA (cccDNA) in the liver, histological improvements, and the rate of ALT normalization.
The rate of HBsAg loss in the treatment group was significantly higher than that of the control group (5.5% 1.8%, =0.031). There were 11.1% of patients in the treatment group who recorded a reduction in HBsAg ≥1 lg·IU/mL, which is better than 5.9% of patients in the control group (=0.043). There was no significant difference between the two groups with regard to the rate of HBV DNA clearance, the reduction in intrahepatic cccDNA, and the rate of ALT normalization ( > 0.05). The rate of liver fibrosis improvement in the treatment group was better than that of the control group (35.5% 11.8%, =0.031), but there was no difference in necroinflammatory improvement ( > 0.05). The adverse events (AEs) were similar between the two groups, except for the abnormal kidney function, with 2.2% in the control group and 0.0% in the treatment group (=0.028).
The combination of BSJPF and ETV can increase the rate of HBsAg loss and the rate of histological fibrosis improvement without serious adverse events in CHB patients. . This trial is registered with ChiCTR-IOR-16009880 on November 16, 2016-retrospectively registered, http://www.chictr.org.cn/showproj.aspx?proj=16836.
补肾健脾方(BSJPF,亦称灵猫方)是一种用于治疗慢性乙型肝炎(CHB)的中药。先前的研究表明,补肾健脾方与恩替卡韦(ETV)联合治疗可使丙氨酸氨基转移酶轻度升高的HBeAg阳性CHB患者的乙肝e抗原(HBeAg)显著转阴,血清乙肝病毒(HBV)DNA水平显著下降。
本研究旨在评估补肾健脾方联合ETV治疗HBeAg阴性CHB患者的疗效和安全性。
总共640例患者按1∶1比例随机分为治疗组(接受补肾健脾方联合ETV治疗96周)或对照组(接受安慰剂联合ETV治疗96周)。主要终点为乙肝表面抗原(HBsAg)转阴率。次要结局包括HBsAg浓度下降至≥1 log₁₀IU/mL的比例、HBV DNA抑制情况、肝脏中cccDNA水平的下降、组织学改善情况以及谷丙转氨酶(ALT)复常率。
治疗组的HBsAg转阴率显著高于对照组(5.5%对1.8%,P = 0.031)。治疗组有11.1%的患者HBsAg下降≥1 log₁₀IU/mL,优于对照组的5.9%(P = 0.043)。两组在HBV DNA清除率、肝内cccDNA下降以及ALT复常率方面无显著差异(P>0.05)。治疗组的肝纤维化改善率优于对照组(35.5%对11.8%,P = 0.031),但在坏死性炎症改善方面无差异(P>0.05)。除肾功能异常外,两组的不良事件(AE)相似,对照组为2.2%,治疗组为0.0%(P = 0.028)。
补肾健脾方联合ETV可提高CHB患者的HBsAg转阴率和组织学纤维化改善率,且无严重不良事件。本试验于2016年11月16日在中国临床试验注册中心注册(ChiCTR - IOR - 16009880,回顾性注册),http://www.chictr.org.cn/showproj.aspx?proj = 16836 。