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通过联合诱导治疗和延长维持治疗实现慢性丙型肝炎的高持续病毒学应答

High sustained virological response in chronic hepatitis C by combining induction and prolonged maintenance therapy.

作者信息

Vrolijk J M, Bekkering F C, Brouwer J T, Hansen B E, Schalm S W

机构信息

Dept of Hepatology & Gastroenterology, Erasmus MC/University Medical Centre Rotterdam, 3000 CA Rotterdam, the Netherlands.

出版信息

J Viral Hepat. 2003 May;10(3):205-9. doi: 10.1046/j.1365-2893.2003.00408.x.

Abstract

Chronic hepatitis C patients with genotype 1 infection, liver cirrhosis, high viral load, or those who have not responded to anti-viral treatment in the past have limited chances of clearing the virus, even with pegylated interferon-ribavirin therapy. In this study we treated such patients with a treatment schedule that combines high dose induction Interferon (IFN), prolonged daily IFN and ribavirin treatment. Twenty-four consecutive patients were included in this study with either genotype 1 infection, cirrhosis, previous non-response to IFN or a combination of these poor-response characteristics. Patients were treated with 10 million units (MU) of IFN daily for 4 weeks followed by 5 MU/day until week 24, 3 MU/day until week 52 and 3 MU thrice weekly until week 76 in combination with 1-1.2 g ribavirin daily. HCV RNA levels were assessed weekly until week 4 and at least once every 3 months thereafter, by a validated assay with a detection limit below 500 copies/mL. Both intention to treat (ITT) and per protocol (PP) analysis showed a high sustained virological response (ITT 67%, PP 80%). A virological response occurred rapidly (before 8 weeks of treatment) in all patients with a sustained response. Relapse after stopping therapy was observed in only 5%. Side-effects were observed frequently, and six patients had to be hospitalized. With this new treatment regimen that combines induction- and prolonged daily interferon treatment with ribavirin it seems possible to eliminate hepatitis C virus in the majority of patients that have an a priori limited chance of sustained response. Further clinical evaluation of intensive interferon and ribavirin combination therapy (now also including PEG-interferon) is recommended in centres that can provide close patient monitoring and experienced hepatological support.

摘要

基因1型感染、肝硬化、病毒载量高的慢性丙型肝炎患者,或过去对抗病毒治疗无反应的患者,即使采用聚乙二醇化干扰素-利巴韦林治疗,清除病毒的机会也有限。在本研究中,我们采用高剂量诱导干扰素(IFN)、延长每日IFN和利巴韦林治疗相结合的治疗方案治疗此类患者。本研究纳入了24例连续的患者,他们要么是基因1型感染,要么是肝硬化,要么既往对IFN无反应,或者具有这些不良反应特征的组合。患者先接受每日1000万单位(MU)的IFN治疗4周,然后每日5 MU直至第24周,每日3 MU直至第52周,每周三次3 MU直至第76周,同时每日联合使用1-1.2 g利巴韦林。每周评估HCV RNA水平直至第4周,此后每3个月至少评估一次,采用检测限低于500拷贝/mL的经过验证的检测方法。意向性分析(ITT)和符合方案分析(PP)均显示出高持续病毒学应答率(ITT为67%,PP为80%)。所有获得持续应答的患者均在治疗8周前迅速出现病毒学应答。仅5%的患者在停药后出现复发。副作用频繁出现,6例患者需要住院治疗。采用这种将诱导和延长每日干扰素治疗与利巴韦林相结合的新治疗方案,似乎有可能在大多数一开始持续应答机会有限的患者中消除丙型肝炎病毒。建议在能够提供密切患者监测和经验丰富的肝病学支持的中心,对强化干扰素和利巴韦林联合治疗(现在也包括聚乙二醇化干扰素)进行进一步的临床评估。

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