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Telbivudine: a review of its use in compensated chronic hepatitis B.

机译:替比夫定:综述其在代偿性慢性乙型肝炎中的用途。

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摘要

Telbivudine (Sebivo(R); Tyzeka(R)) is a synthetic nucleoside analogue that inhibits replication of hepatitis B virus (HBV). It is used in the treatment of adults with chronic hepatitis B (CHB) with evidence of viral replication and persistently elevated serum ALT and/or AST levels, and/or histological evidence of active disease. Telbivudine is a potent antiviral that provides effective and sustained viral suppression in patients with compensated CHB. In clinical trials, treatment outcomes were improved significantly more with telbivudine 600 mg once daily than with lamivudine 100 mg or adefovir 10 mg once daily, and telbivudine-treated patients had significantly less viral resistance than lamivudine-treated patients. Increasing rates of hepatitis B e antigen (HBeAg) seroconversion were achieved in HBeAg-positive patients during periods of up to 4 years continuous telbivudine treatment, and seroconversion was durable in most patients throughout a 2-year, off-treatment follow-up, indicating the potential for a finite treatment period in this group of patients. Telbivudine is associated with a medium genetic barrier to resistance and, as patients with undetectable HBV DNA levels have significantly improved outcomes, it is recommended that HBV DNA levels are monitored at week 24 (and 6 monthly thereafter), with the addition of a nucleosideucleotide analogue without cross resistance (such as adefovir dipivoxil) if viraemia is present to reduce the risk of resistance (Roadmap concept). Telbivudine was generally well tolerated in clinical trials for periods of up to 4 years, and has a similar tolerability profile to that of lamivudine. A minority of telbivudine-treated patients experience creatinine kinase elevation, usually transient, and myopathy occurs rarely. In modelled cost effectiveness studies in several Asian countries, treatment with telbivudine Roadmap was cost effective in HBeAg-positive patients. Thus, telbivudine provides a valuable treatment option in CHB, particularly when administered using the Roadmap concept in HbeAg-positive patients.
机译:替比夫定(Sebivo®;Tyzeka®)是一种合成的核苷类似物,可抑制乙型肝炎病毒(HBV)的复制。它用于治疗具有病毒复制和血清ALT和/或AST水平持续升高和/或活动性疾病的组织学证据的慢性乙型肝炎(CHB)成人。替比夫定是一种有效的抗病毒药,可为代偿性CHB患者提供有效和持续的病毒抑制。在临床试验中,每日一次600mg替比夫定的治疗效果比每日一次拉米夫定100mg或阿德福韦10mg的治疗效果明显改善,并且替比夫定治疗的患者的病毒抵抗力明显低于拉米夫定治疗的患者。在长达4年的连续替比夫定治疗期间,HBeAg阳性患者的乙型肝炎e抗原(HBeAg)血清转化率增加,并且在整个2年的非治疗随访中,大多数患者的血清转化率持久。该组患者有限治疗期的潜力。替比夫定与抵抗力的中等遗传障碍有关,并且由于无法检测到的HBV DNA水平具有明显改善的结局,建议在第24周(此后每月6个月)监测HBV DNA水平,并添加核苷/如果存在病毒血症以降低耐药风险,则无交叉耐药的核苷酸类似物(例如阿德福韦酯)。替比夫定在临床试验中通常可以耐受长达4年,并且具有与拉米夫定相似的耐受性。少数接受替比夫定治疗的患者的肌酐激酶升高,通常是短暂的,肌病很少发生。在几个亚洲国家进行的成本效益模型研究中,替比夫定路线图治疗对HBeAg阳性患者具有成本效益。因此,替比夫定在CHB中提供了一种有价值的治疗选择,尤其是在HbeAg阳性患者中使用Roadmap概念给药时。

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