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对于 HCV 基因型 1 且病毒载量较高、在 24 周后才获得病毒学应答的患者,延长 PEG-IFN 和 RBV 的疗程是有效的。

Prolonged PEG-IFN and RBV is effective in patients with HCV genotype 1 and high viral load who achieved virological response later than 24 weeks.

机构信息

Department of Gastroenterology and Hepatology, Kinki University School of Medicine, Osaka-Sayama, Osaka, Japan.

出版信息

Intervirology. 2010;53(1):55-9. doi: 10.1159/000252785. Epub 2010 Jan 5.

Abstract

OBJECTIVE

The extension of treatment duration has been proposed in late virological responders with hepatitis C virus (HCV) genotype 1 and high viral load. However, the effectiveness of extended treatment in patients whose serum HCV RNA become undetectable later than 24 weeks of treatment (ultra-late virological responder; ULVR) has not yet been determined.

METHODS

A total of 130 patients infected with HCV genotype 1 and who had high viral load were treated with pegylated interferon (PEG-IFN) and ribavirin (RBV) combination therapy. We retrospectively analyzed 10 ULVR who received extended combination treatment beyond 48 weeks.

RESULTS

The duration of the combination treatment for ULVR ranged between 59 and 119 weeks, and the mean duration was 80 weeks. Although the majority of ULVR were older female patients (> or = 60 years) with factors related to poor therapeutic response, 8 patients (80%) achieved sustained virological response (SVR). The SVR rate correlated well with the duration of the treatment. Five ULVR achieved SVR when treatment was continued until serum HCV RNA remained undetectable for longer than 48 weeks.

CONCLUSION

The extended duration of PEG-IFN and RBV combination treatment is a possible strategy to improve treatment response in HCV genotype 1 infection, even for ULVR.

摘要

目的

对于丙型肝炎病毒(HCV)基因型 1 且病毒载量较高的病毒学应答延迟患者,已经提出延长治疗时间。然而,对于那些在治疗 24 周后 HCV RNA 才转为不可检测的患者(超晚病毒学应答者;ULVR),延长治疗的有效性尚未确定。

方法

共有 130 例感染 HCV 基因型 1 且病毒载量较高的患者接受了聚乙二醇干扰素(PEG-IFN)和利巴韦林(RBV)联合治疗。我们回顾性分析了 10 例接受超过 48 周的延长联合治疗的 ULVR。

结果

ULVR 的联合治疗持续时间为 59 至 119 周,平均持续时间为 80 周。虽然大多数 ULVR 为年龄较大的老年女性(≥60 岁),伴有与治疗应答不良相关的因素,但有 8 例(80%)患者获得持续病毒学应答(SVR)。SVR 率与治疗持续时间密切相关。当治疗持续时间超过 48 周且血清 HCV RNA 持续不可检测时,有 5 例 ULVR 获得了 SVR。

结论

PEG-IFN 和 RBV 联合治疗的延长时间可能是提高 HCV 基因型 1 感染治疗反应的一种策略,即使是针对 ULVR。

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