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慢性丙型肝炎的再治疗:对象与方法?

Retreatment of chronic hepatitis C: who and how?

作者信息

Heathcote Jenny

机构信息

University of Toronto, Toronto, ON, Canada.

出版信息

Liver Int. 2009 Jan;29 Suppl 1:49-56. doi: 10.1111/j.1478-3231.2008.01932.x.

Abstract

All but about 10% of patients with chronic hepatitis C (CHC) (predominantly those infected with genotype 1) can respond to some degree to 'combination' therapy with interferon (IFN) and ribavirin. The slower the virological response to treatment, the less likely sustained viral clearance will take place. Many factors influence response to antiviral therapy; most cannot be reversed (e.g. sex, age, cirrhosis, genotype and viral load). A sustained viral clearance is considerably facilitated by compliance with full-dose therapy for the prescribed time. The potential cause(s) for non-response need(s) to be ascertained before attempting retreatment. The 10% of patients who are true 'null' responders may respond to the new specifically targeted antiviral therapies but whether the response can be sustained off-therapy is unclear. Adjunctive therapies may facilitate response to retreatment if intolerance to treatment leading to diminished or absent doses was problematic in the past. Retreatment with a long-acting IFN and an adequate ribavirin dose (15 mg/kg), but given for 72 weeks in prior relapsers following 48 weeks of treatment, will enhance sustained virological response (SVR) rates. No benefit is gained from changing one pegylated IFNalpha (PEG IFNalpha) to another unless the treatment duration is extended. Only alpha-interferons are effective. For those individuals who still fail to achieve SVR, recruitment to trials of new treatments should be encouraged particularly for those with advanced liver disease. Lifestyle modification may be appropriate in attempt to reduce the chance of complications of liver disease, namely hepatocellular carcinoma, by smoking cessation, eliminating obesity and increasing coffee consumption.

摘要

除了约10%的慢性丙型肝炎(CHC)患者(主要是感染基因1型的患者)外,所有患者都能对干扰素(IFN)和利巴韦林的“联合”疗法产生一定程度的反应。治疗的病毒学反应越慢,持续病毒清除的可能性就越小。许多因素会影响对抗病毒治疗的反应;大多数因素无法逆转(如性别、年龄、肝硬化、基因型和病毒载量)。在规定时间内坚持全剂量治疗可大大促进持续病毒清除。在尝试再次治疗之前,需要确定无反应的潜在原因。10%的真正“无反应”患者可能对新的特异性靶向抗病毒疗法有反应,但停药后反应能否持续尚不清楚。如果过去因不耐受治疗导致剂量减少或未用药是个问题,辅助治疗可能有助于再次治疗的反应。对于先前复发的患者,在治疗48周后用长效IFN和足够剂量的利巴韦林(15mg/kg)再治疗72周,将提高持续病毒学应答(SVR)率。除非延长治疗时间,否则将一种聚乙二醇化干扰素α(PEG IFNα)换成另一种没有益处。只有α干扰素是有效的。对于那些仍未实现SVR的个体,应鼓励他们参加新治疗方法的试验,特别是对于那些患有晚期肝病的患者。通过戒烟、消除肥胖和增加咖啡摄入量来改变生活方式,可能有助于降低肝病并发症(即肝细胞癌)的发生几率。

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