对聚乙二醇化干扰素和利巴韦林无反应的患者每日高剂量一致干扰素的再治疗。

Hepatitis research and treatment Pub Date : 2010-01-01 Epub Date: 2010-10-10 DOI:10.1155/2010/537827
Douglas F Meyer, Hillel Tobias, Albert D Min, Arathi Rajendra, Ivanka Zic, Edward Brettholz, David J Clain, Franklin Klion, David Bernstein, Henry C Bodenheimer
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引用次数: 2

摘要

背景。目前使用聚乙二醇化干扰素和利巴韦林治疗慢性丙型肝炎能够消除大约一半的治疗患者的病毒感染。在未来出现新的抗病毒药物之前,对剩余慢性肝炎患者的治疗选择仍然有限。共识干扰素目前可用,并已证明具有优异的体外抗病毒活性的临床疗效,但最大耐受剂量尚未确定。方法。我们评估了每日高剂量(24 ug)共识干扰素与基于体重的(1000-1200 mg /天)利巴韦林在HCV基因型1感染无应答患者中的疗效。结果。在5名患者中记录了6个不良事件,试验在没有受试者达到病毒清除的情况下终止。结论。严重不良事件的发生有效地确定了可接受剂量的上限,同时也揭示了该剂量不能提供增强的持续病毒清除。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Retreatment of patients nonresponsive to pegylated interferon and ribavirin with daily high-dose consensus interferon.

Retreatment of patients nonresponsive to pegylated interferon and ribavirin with daily high-dose consensus interferon.

Background. Current treatment of chronic hepatitis C with pegylated interferon and ribavirin has the ability to eliminate viral infection in about half of the patients treated. Therapeutic options, for those with remaining chronic hepatitis, will remain limited until novel antivirals become available in the future. Consensus interferon is currently available and has demonstrated clinical efficacy with superior invitro antiviral activity, but the maximum tolerated dose is not defined. Methods. We assessed the efficacy of daily high-dose (24 ug) consensus interferon with weight-based (1000-1200 mg daily) ribavirin in HCV genotype 1-infected non-responder patients. Results. Six adverse events were documented in five patients, and the trial was terminated with no subject achieving viral clearance. Conclusions. The occurrence of serious adverse events effectively defined the upper limit of acceptable dose, while also revealing that this dose did not offer enhanced sustained viral clearance.

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