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一项关于重组人白细胞介素12治疗既往治疗无反应的慢性丙型肝炎病毒感染患者的多中心研究。

A multicenter study of recombinant human interleukin 12 for the treatment of chronic hepatitis C virus infection in patients nonresponsive to previous therapy.

作者信息

Pockros Paul J, Patel Keyvr, O'Brien Christopher, Tong Myron, Smith Coleman, Rustgi Vinod, Carithers Robert L, McHutchison John G, Olek Elizabeth, Debruin Michael F

机构信息

Division of Gastroenterology and Hepatology, Scripps Clinic, La Jolla, CA, USA.

出版信息

Hepatology. 2003 Jun;37(6):1368-74. doi: 10.1053/jhep.2003.50242.

Abstract

Recombinant human interleukin 12 (IL-12) is an immunomodulatory cytokine that is active against several viruses. Treatment options in patients with chronic hepatitis C with nonresponse to interferon (IFN)-based therapy are limited. Prior dose-ranging studies have indicated drug tolerability and transient suppression of hepatitis C virus (HCV) RNA by IL-12. The aim of this study was to determine the safety and efficacy of prolonged IL-12 therapy in patients who have failed treatment with IFN-alpha +/- ribavirin. A total of 225 patients at 21 U.S. sites who had a history of nonresponse to IFN-alpha or combination IFN-alpha plus ribavirin for treatment of HCV were randomized to 500 ng/kg IL-12 or placebo subcutaneously twice weekly for 12 weeks. The groups were then unblinded; patients receiving IL-12 continued for another 36 weeks, and the placebo group received 48 weeks of treatment with IL-12 in an open-label fashion. HCV RNA, serum alanine aminotransferase (ALT) level, and a repeat liver biopsy were assessed at 24 weeks following therapy. Approximately 1% (2 of 160) of nonresponsive patients enrolled for treatment had a sustained virologic response to IL-12 therapy, but 3% (7 of 225) developed severe adverse events probably related to treatment, resulting in early termination of the trial. Common adverse effects reported by most patients included chills, fever, fatigue, headache, and arthralgia. At termination of the study, 160 patients had received at least 8 weeks of treatment with IL-12. Paired liver biopsy specimens were available for evaluation in 54 patients, but there were no significant changes in Knodell fibrosis or histologic activity index (HAI) scores. In conclusion, IL-12 as monotherapy at the doses used in this trial for chronic hepatitis C has low efficacy, was poorly tolerated, and is unlikely to provide an alternative to conventional IFN-based therapy.

摘要

重组人白细胞介素12(IL-12)是一种免疫调节细胞因子,对多种病毒具有活性。对基于干扰素(IFN)的治疗无反应的慢性丙型肝炎患者的治疗选择有限。先前的剂量范围研究表明IL-12具有药物耐受性并能短暂抑制丙型肝炎病毒(HCV)RNA。本研究的目的是确定在接受IFN-α±利巴韦林治疗失败的患者中延长IL-12治疗的安全性和有效性。在美国21个地点的总共225例有对IFN-α或IFN-α联合利巴韦林治疗HCV无反应病史的患者被随机分为皮下注射500 ng/kg IL-12或安慰剂,每周两次,共12周。然后对分组进行揭盲;接受IL-12治疗的患者继续治疗另外36周,安慰剂组以开放标签方式接受48周的IL-12治疗。在治疗后24周评估HCV RNA、血清丙氨酸氨基转移酶(ALT)水平和重复肝活检。纳入治疗的无反应患者中约1%(160例中的2例)对IL-12治疗有持续病毒学应答,但3%(225例中的7例)发生可能与治疗相关的严重不良事件,导致试验提前终止。大多数患者报告的常见不良反应包括寒战、发热、疲劳、头痛和关节痛。在研究结束时,160例患者接受了至少8周的IL-12治疗。54例患者有配对的肝活检标本可供评估,但Knodell纤维化或组织学活动指数(HAI)评分无显著变化。总之,本试验中用于慢性丙型肝炎的剂量的IL-12单药治疗疗效低、耐受性差,不太可能替代传统的基于IFN的治疗。

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