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首页> 外文期刊>Transplantation: Official Journal of the Transplantation Society >Treatment of recurrent hepatitis C infection after liver transplantation with combination of pegylated interferon alpha2b and ribavirin: an open-label series.
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Treatment of recurrent hepatitis C infection after liver transplantation with combination of pegylated interferon alpha2b and ribavirin: an open-label series.

机译:聚乙二醇化干扰素α2b和利巴韦林联合治疗肝移植后复发的丙型肝炎感染:开放标签系列。

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BACKGROUND: Hepatitis C virus (HCV) recurrence after orthotopic liver transplantation (OLT) is universal. We aimed to evaluate the efficacy and safety of pegylated interferon (PEG-IFN) and ribavirin (RIB) in the treatment of post-OLT HCV recurrence. METHODS: Thirty-seven patients with recurrent HCV after OLT were screened and began treatment. Nineteen patients have completed therapy. PEG-IFN was started at a dose of 0.5 microg/kg per week and titrated toward a maximum dose of 1.5 microg/kg per week. RIB was started at a dose of 400 mg per day and titrated toward a maximum of 1000 mg per day, as tolerated. Therapy continued for 1 year after HCV replication was undetectable by reverse transcriptase-polymerase chain reaction and was discontinued if there was no virologic clearance at 48 weeks. RESULTS: Twelve patients (63%) completed the combination regimen. Therapy was discontinued in seven (37%) patients. Seven patients (37%) had undetectable viral load at the end of treatment. Of those, five patients (26%) had sustained viral response 6 months after discontinuation of therapy. Five patients (26%) had no virologic response. Necro-inflammatory score declined from 5.22 to 2.89 (P=0.05) in nonresponders versus 6.8 to 2.6 (P<0.01) in responders. Fibrosis stage did not change in either group. Genotype 1-infected patients had a lower likelihood of attaining end of treatment or sustained viral response (P<0.05 for both). CONCLUSIONS: Post-OLT HCV recurrence can be safely treated with PEG-IFN and RIB. Bone marrow toxicity, depression, and rejection are limiting factors that require aggressive management. There was short-term histologic benefit to the use of this regimen, even in those patients without viral clearance.
机译:背景:原位肝移植(OLT)后丙型肝炎病毒(HCV)复发是普遍的。我们旨在评估聚乙二醇干扰素(PEG-IFN)和利巴韦林(RIB)在OLT后HCV复发中的疗效和安全性。方法:对37例OLT术后复发的HCV患者进行筛查并开始治疗。 19位患者已完成治疗。 PEG-IFN以每周0.5微克/千克的剂量开始,并朝着每周1.5微克/千克的最大剂量滴定。 RIB以每天400 mg的剂量开始,并按耐受的最大每日1000 mg滴定。 HCV复制不能通过逆转录酶-聚合酶链反应检测到后继续治疗1年,如果在48周内没有病毒清除,则停止治疗。结果:十二名患者(63%)完成了联合治疗方案。七名(37%)患者停止治疗。 7名患者(37%)在治疗结束时具有无法检测到的病毒载量。其中,五名患者(26%)在停止治疗后六个月持续病毒反应。五名患者(26%)没有病毒学应答。无反应者的炎症反应评分从5.22降至2.89(P = 0.05),而反应者则为6.8至2.6(P <0.01)。两组的纤维化阶段均未改变。被基因型1感染的患者达到治疗终止或持续病毒应答的可能性较低(两者均P均<0.05)。结论:PEG-IFN和RIB可安全治疗OLT后HCV复发。骨髓毒性,抑郁和排斥是需要积极治疗的限制因素。即使没有病毒清除的患者,使用该方案也有短期的组织学益处。

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