Peginterferon alfa-2a for hepatitis C after liver transplantation: Two randomized, controlled trials

被引:185
作者
Chalasani, N
Manzarbeitia, C
Ferenci, P
Vogel, W
Fontana, RJ
Voigt, M
Riely, C
Martin, P
Teperman, L
Jiao, J
Lopez-Talavera, JC
机构
[1] Indiana Univ, Sch Med, Med Ctr, Indianapolis, IN 46202 USA
[2] Albert Einstein Med Ctr, Philadelphia, PA 19141 USA
[3] Univ Vienna, A-1010 Vienna, Austria
[4] Univ Innsbruck, A-6020 Innsbruck, Austria
[5] Univ Michigan, Med Ctr, Ann Arbor, MI 48109 USA
[6] Univ Iowa Hosp & Clin, Iowa City, IA 52242 USA
[7] Univ Tennessee, Memphis, TN 38163 USA
[8] Cedars Sinai Med Ctr, Los Angeles, CA 90048 USA
[9] NYU, Med Ctr, New York, NY 10016 USA
[10] Roche Labs Inc, Nutley, NJ USA
关键词
D O I
10.1002/hep.20560
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
There is currently no effective treatment for recurrent hepatitis C after orthotopic liver transplantation (OLT). We therefore performed two randomized, controlled trials-a prophylaxis trial and a treatment trial-to evaluate the safety and efficacy of peginterferon alfa-2a in patients who had undergone OLT. The prophylaxis trial enrolled 54 patients within 3 weeks after OLT, and the treatment trial enrolled 67 patients 6 to 60 months after OLT. In each trial, patients were randomized to treatment with once weekly injections of 180 jug peginterferon alfa-2a or no antiviral treatment for 48 weeks and were followed up for 24 weeks thereafter. Peginterferon alfa-2a treated patients had significantly lower hepatitis C virus RNA levels and more favorable changes in hepatic histological features compared with untreated controls. However, only 2 treated patients in the prophylaxis trial (8%) and 3 in the treatment trial (12%) achieved a sustained virological response. In the prophylaxis trial, 8 patients (31%) in the peginterferon alfa-2a group and 9 (32%) in the untreated group were withdrawn prematurely; whereas in the treatment trial, 10 patients (30%) in the peginterferon alfa-2a group and 6 (19%) in the untreated group were withdrawn prematurely. The incidence of acute rejection was similar in the treated and untreated groups in both the prophylaxis (12% vs. 21%; P = .5) and treatment (12% vs. 0%; P = .1) trials. In conclusion, peginterferon alfa-2a treatment for 48 weeks is safe and tolerable and offers some efficacy in the post-OLT setting. Randomized controlled studies are needed to establish the efficacy of pegylated interferon and ribavirin in patients who have undergone OLT.
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收藏
页码:289 / 298
页数:10
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