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Telbivudine versus lamivudine in Chinese patients with chronic hepatitis B: Results at 1 year of a randomized, double-blind trial

替比夫定 拉米夫定 医学 胃肠病学 HBeAg 内科学 乙型肝炎病毒 乙型肝炎 核苷类似物 血清转化 免疫学 病毒 乙型肝炎表面抗原 核苷 生物 生物化学
作者
Jinlin Hou,You-Kuan Yin,Dao-zhen Xu,Deming Tan,Junqi Niu,Xia-Qiu Zhou,Yuming Wang,Li-Min Zhu,Yong-Wen He,Hong Ren,Mobin Wan,Cheng-Wei Chen,Shanming Wu,Ya-gang Chen,Jia-Zhang Xu,Qinhuan Wang,Lai Wei,George Y. Chao,Barbara Fielman Constance,George Harb,Nathaniel A. Brown,Jidong Jia
出处
期刊:Hepatology [Lippincott Williams & Wilkins]
卷期号:47 (2): 447-454 被引量:149
标识
DOI:10.1002/hep.22075
摘要

Chronic hepatitis B and its life-threatening sequelae are highly prevalent in China. There is a need for effective new therapies to suppress hepatitis B virus (HBV) replication and ameliorate liver disease. In this study, we compared the efficacy of telbivudine, a nucleoside analogue, with lamivudine in Chinese patients. In this phase III, double-blind, multicenter trial conducted in China, 332 patients with compensated hepatitis B e antigen (HBeAg)-positive or HBeAg-negative chronic hepatitis B were randomly assigned to treatment with 600 mg of telbivudine or 100 mg of lamivudine daily for 104 weeks. The primary efficacy endpoint was reduction in serum HBV DNA levels at week 52 of treatment. Secondary endpoints included clearance of HBV DNA to undetectable levels, HBeAg loss and seroconversion, therapeutic response, and alanine aminotransferase (ALT) normalization. Viral resistance and safety were assessed. At week 52, among 290 HBeAg-positive patients, mean reductions of serum HBV DNA were significantly greater in telbivudine recipients than lamivudine recipients (6.3 log(10) versus 5.5 log(10), P < 0.001), and HBV DNA was polymerase chain reaction-negative in significantly more telbivudine recipients than lamivudine recipients (67% versus 38%, P < 0.001). ALT normalization (87% versus 75%, P = 0.007), therapeutic response (85% versus 62%, P = 0.001), and HBeAg loss (31% versus 20%, P = 0.047) were also significantly more common in the telbivudine group. Treatment effects showed similar patterns in the smaller HBeAg-negative group (n = 42). Viral resistance in telbivudine recipients was approximately half that observed with lamivudine; however, this difference was not statistically significant. Clinical adverse events were similar in the two treatment groups.In Chinese patients with chronic hepatitis B, telbivudine treatment for 52 weeks provided greater antiviral and clinical efficacy than lamivudine, with less resistance.
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