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肝移植术后复发丙型肝炎患者应用小剂量聚乙二醇干扰素维持治疗的效果。

Effect of maintenance therapy with low-dose peginterferon for recurrent hepatitis C after living donor liver transplantation.

机构信息

Department of Gastroenterology and Hepatology, Kyoto University, Shogoin, Sakyo-ku, Kyoto, Japan.

出版信息

J Viral Hepat. 2012 Jan;19(1):32-8. doi: 10.1111/j.1365-2893.2010.01398.x. Epub 2010 Dec 3.

Abstract

Approximately 30% of patients who have recurrent hepatitis C after liver transplantation achieve sustained virological response (SVR) by taking a combination therapy of pegylated interferon and ribavirin. For the remaining non-SVR patients, an effective management treatment has not yet been established. In this study, efficacy of long-term peginterferon maintenance therapy for non-SVR patients was evaluated. Forty patients who had previously received the combination therapy for hepatitis C after living donor liver transplantation were classified into one of the following three groups: the SVR group (n = 11); the non-SVR-IFN group (n =17), which received low-dose peginterferon maintenance therapy for non-SVR patients; and the non-SVR-Withdrawal group (n = 12), which discontinued the interferon treatment. We then compared histological changes among these three groups after 2 or more years follow-up. Activity grade of liver histology improved or remained stable in patients in the SVR and non-SVR-IFN groups, but deteriorated in half of the patients in the non-SVR-Withdrawal group. Fibrosis improved or remained stable in 10 of 11 SVR patients and in 13 of 17 non-SVR-IFN patients, but deteriorated in all non-SVR-Withdrawal patients. Mean changes in fibrosis stage between pretreatment and final liver biopsy were -0.18, +0.06 and +2.2 in the SVR, non-SVR-IFN and non-SVR-Withdrawal groups, respectively. Fibrosis stage deteriorated to F3 or F4 significantly more rapidly in the non-SVR-Withdrawal group than in the other two groups. In conclusion, continuing long-term maintenance therapy with peginterferon prevented histological progression of hepatitis C in patients who had undergone living donor liver transplantation.

摘要

约 30%的肝移植后复发丙型肝炎患者通过接受聚乙二醇干扰素和利巴韦林联合治疗实现持续病毒学应答(SVR)。对于其余未达到 SVR 的患者,尚未建立有效的治疗管理方法。本研究评估了长期聚乙二醇干扰素维持治疗对未达到 SVR 的患者的疗效。将 40 例先前接受过活体供肝移植后丙型肝炎联合治疗的患者分为以下三组:SVR 组(n=11);非 SVR-IFN 组(n=17),该组为未达到 SVR 的患者接受低剂量聚乙二醇干扰素维持治疗;非 SVR-停药组(n=12),该组停止干扰素治疗。然后,我们在 2 年以上的随访后比较了三组之间的组织学变化。SVR 和非 SVR-IFN 组的患者肝组织学活动评分改善或保持稳定,但非 SVR-停药组的一半患者评分恶化。11 例 SVR 患者中有 10 例和 17 例非 SVR-IFN 患者中有 13 例纤维化改善或保持稳定,但所有非 SVR-停药患者纤维化均恶化。SVR、非 SVR-IFN 和非 SVR-停药组治疗前后纤维化分期的平均变化分别为-0.18、+0.06 和+2.2。非 SVR-停药组纤维化分期恶化到 F3 或 F4 的速度明显快于其他两组。总之,继续长期接受聚乙二醇干扰素维持治疗可预防活体供肝移植后丙型肝炎患者的组织学进展。

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