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聚乙二醇化干扰素α-2a联合利巴韦林递增剂量方案在肝移植后丙型肝炎病毒再感染早期阶段的疗效

Efficacy of an escalating dose regimen of pegylated interferon alpha-2a plus ribavirin in the early phase of HCV reinfection after liver transplantation.

作者信息

Zimmermann Tim, Böcher Wulf O, Biesterfeld Stefan, Zimmermann Anca, Kanzler Stefan, Greif-Higer Gertrud, Barreiros Ana Paula, Sprinzl Martin F, Wörns Marcus A, Lohse Ansgar W, Mönch Christian, Otto Gerd, Galle Peter R, Schuchmann Marcus

机构信息

1st Department of Medicine, University of Mainz, Langenbeck Strasse 1, 55101 Mainz, Germany.

出版信息

Transpl Int. 2007 Jul;20(7):583-90. doi: 10.1111/j.1432-2277.2007.00481.x. Epub 2007 Apr 13.

Abstract

We evaluated the safety and efficacy of an escalating dose regimen of pegylated interferon alpha-2a (PEG-IFN(alpha-2a)) and ribavirin in the early phase of recurrent hepatitis C after orthotopic liver transplantation (OLT). In this prospective study, 26 patients transplanted for hepatitis C virus cirrhosis with recurrent hepatitis C were treated 3.4 +/- 3.6 months after OLT and compared with an untreated historical control. PEG-IFN(alpha-2a) was initiated as monotherapy, following stepwise dose escalation up to 180 mug/week and the addition of ribavirin up to 1200 mg/day or maximally tolerated doses for 48 weeks. In the intent-to-treat analysis, 38% showed an early virological response (EVR), 35% an end of treatment response (ETR) and 19% a sustained virological response (SVR). SVR was associated with EVR (P = 0.0001) and cumulative PEG-IFN(alpha-2a) dose (P = 0.04). There was no significant histological improvement compared with untreated patients. There were no treatment-related serious adverse events. Adverse events included leucopenia (77%) and thrombocytopenia (46%). Three patients discontinued therapy due to side effects, fourteen were nonresponders and four relapsers. Treatment with PEG-IFN(alpha-2a) and ribavirin in the acute phase of post-transplant recurrent hepatitis C yielded an EVR of 38% and an SVR of 19%. The combination was safe and well tolerated.

摘要

我们评估了聚乙二醇化干扰素α-2a(PEG-IFNα-2a)与利巴韦林递增剂量方案在原位肝移植(OLT)后复发性丙型肝炎早期阶段的安全性和疗效。在这项前瞻性研究中,26例因丙型肝炎病毒肝硬化接受移植且发生复发性丙型肝炎的患者在OLT后3.4±3.6个月接受治疗,并与未经治疗的历史对照进行比较。PEG-IFNα-2a开始作为单一疗法,逐步递增剂量至180μg/周,并加用利巴韦林至1200mg/天或最大耐受剂量,持续48周。在意向性治疗分析中,38%的患者表现出早期病毒学应答(EVR),35%表现出治疗结束时应答(ETR),19%表现出持续病毒学应答(SVR)。SVR与EVR(P = 0.0001)和累积PEG-IFNα-2a剂量(P = 0.04)相关。与未治疗的患者相比,组织学改善不显著。没有与治疗相关的严重不良事件。不良事件包括白细胞减少(77%)和血小板减少(46%)。3例患者因副作用停药,14例无应答,4例复发。在移植后复发性丙型肝炎急性期使用PEG-IFNα-2a和利巴韦林治疗,EVR为38%,SVR为19%。该联合治疗安全且耐受性良好。

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