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干扰素 -γ联合聚乙二醇干扰素α-2a 和利巴韦林治疗慢性丙型肝炎无应答患者(ANRS HC16 GAMMATRI)。

Interferon-gamma with peginterferon alpha-2a and ribavirin in nonresponder patients with chronic hepatitis C (ANRS HC16 GAMMATRI).

机构信息

CHU de Bordeaux, Pessac, France.

出版信息

J Gastroenterol Hepatol. 2013 Feb;28(2):329-34. doi: 10.1111/jgh.12060.

Abstract

BACKGROUND AND AIM

Interferon-gamma-1b (IFN-γ-1b) improves alpha interferon (IFN-α) inhibition of hepatitis C virus (HCV) replication in replicon system. We described virological response after addition of IFN-γ to a combination of ribavirin/peginterferon (PEG-IFN)-α-2a or α-2b.

METHODS

In this non-comparative, multicenter trial, patients chronically infected by HCV who were nonresponders to a previous treatment by PEG-IFN and ribavirin were restarted on a regimen of PEG-IFN-α-2a (180 μg/week) + ribavirin (1000-1200 mg/day) for 16 weeks. If HCV-RNA decreased less than 2 log(10) copies/mL (nonresponders), and if PEG-IFN-α-2a and ribavirin dosages were unchanged while tolerance was good, IFNγ-1b (100 μg three times per week) was added for the last 32 weeks of treatment. Virological response was evaluated at week 28 (12 weeks after initiation of IFN-γ-1b).

RESULTS

Among the 48 patients started on dual therapy, 23 patients (47%) were nonresponders at week 12 and received IFN-γ-1b from week 16 onward. Their mean HCV-RNA (log(10) IU/mL) was 6.83 at baseline, 5.81 at week 12, and 5.63 at week 28. No patient reached undetectable HCV-RNA at week 28 (upper bound of 95% confidence interval: 14.8%); none had a decrease > 1 log(10) IU/mL. One case of grade 4 neutropenia was reported.

CONCLUSION

Among the strictly selected nonresponders, IFN-γ-1b (at a dosage of 100 μg thrice a week) in combination with PEG-IFN-α-2a and ribavirin failed to show virological efficacy.

摘要

背景与目的

γ干扰素-1b(IFN-γ-1b)可增强α干扰素(IFN-α)对复制子系统中丙型肝炎病毒(HCV)复制的抑制作用。我们描述了在利巴韦林/聚乙二醇干扰素(PEG-IFN)-α-2a 或 α-2b 联合治疗中添加 IFN-γ 后的病毒学应答。

方法

在这项非对照、多中心试验中,对先前接受 PEG-IFN 和利巴韦林治疗无应答的慢性 HCV 感染患者,重新开始使用 PEG-IFN-α-2a(180μg/周)+利巴韦林(1000-1200mg/天)治疗 16 周。如果 HCV-RNA 下降小于 2log10 拷贝/ml(无应答者),并且在耐受性良好的情况下 PEG-IFN-α-2a 和利巴韦林剂量不变,则在治疗的最后 32 周添加 IFN-γ-1b(每周 3 次,每次 100μg)。在开始 IFN-γ-1b 治疗后的第 28 周(12 周后)评估病毒学应答。

结果

在开始双重治疗的 48 例患者中,有 23 例(47%)在第 12 周时无应答,并从第 16 周开始接受 IFN-γ-1b 治疗。他们的平均 HCV-RNA(log10IU/mL)基线时为 6.83,第 12 周时为 5.81,第 28 周时为 5.63。第 28 周时没有患者达到 HCV-RNA 不可检测(95%置信区间上限:14.8%);无一例患者的下降超过 1log10IU/mL。报告了 1 例 4 级中性粒细胞减少症。

结论

在严格选择的无应答者中,PEG-IFN-α-2a 和利巴韦林联合 IFN-γ-1b(剂量为每周 3 次,每次 100μg)未能显示病毒学疗效。

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