Taylor & Francis Group
Browse
ierz_a_1760843_sm9119.docx (499.77 kB)

Nucleos(t)ide analogues for the treatment of chronic hepatitis B: a systematic review with network meta-analysis

Download (499.77 kB)
journal contribution
posted on 2020-05-12, 09:52 authored by JinSong Geng, HaiNi Bao, YaLan Chen, LiLi Shi, Jing Geng, Qing Wang, Hao Yu

Chronic hepatitis B (CHB) is a major global health problem caused by hepatitis B virus (HBV) infection, and can put patients at high risk of death from cirrhosis and liver cancer. However, CHB can be treated with nucleos(t)ide analogues. We aimed to evaluate the effectiveness and safety of nucleos(t)ide analogues for the treatment of CHB patients.

A systematic literature search was performed. Direct comparison meta-analyses and network meta-analysis (NMA) were carried out.

Thirty-six randomized controlled trials (RCTs) met inclusion criteria. Compared with placebo, the nucleos(t)ide analogues were all effective in HBeAg seroconversion, HBeAg loss, and achieving undetectable HBV DNA. Telbivudine was associated with higher HBeAg seroconversion compared with entecavir. For HBeAg loss rate and proportion of achieving undetectable HBV DNA, tenofovir ranked as the best. Entecavir might be the most potent in the normalization of alanine aminotransferase (ALT). The nucleos(t)ide analogues did not have higher serious adverse events rate as compared with placebo.

The nucleos(t)ide analogues are all effective for HBeAg seroconversion, HBeAg loss, undetectable HBV DNA, and most are effective for ALT normalization in adults with CHB. RCTs of multi-center, low risk of bias, and long-term follow-up are still needed.

Funding

This paper was funded by the National Natural Science Foundation of China (Project No. 71603138); Jiangsu Overseas Visiting Scholar Program for University Prominent Young & Middle-aged Teachers and Presidents; Bristol-Myers Squibb Shanghai Pharmaceutical Co., Ltd.

History