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肝移植后复发性丙型肝炎的利巴韦林/α干扰素序贯治疗

Ribavirin/interferon-alpha sequential treatment of recurrent hepatitis C after liver transplantation.

作者信息

Giostra Emiliano, Kullak-Ublick Gerd A, Keller Walter, Fried Ronald, Vanlemmens Claire, Kraehenbuhl Stephan, Locher Sandrine, Egger Hans-Peter, Clavien Pierre-Alain, Hadengue Antoine, Mentha Gilles, Morel Philippe, Negro Francesco

机构信息

Division of Gastroenterology and Hepatology, University Hospital of Geneva, rue Micheli-du-Crest 24, 1211 Geneva, Switzerland.

出版信息

Transpl Int. 2004 May;17(4):169-76. doi: 10.1007/s00147-004-0695-6. Epub 2004 Apr 2.

Abstract

Hepatitis C virus (HCV) infection invariably recurs after liver transplantation (LT), and sequels of chronic hepatitis of the graft are a significant cause of morbidity and mortality. In an uncontrolled trial, 31 patients with histologically confirmed hepatitis C after LT received, sequentially, ribavirin (10 mg/kg body weight q.d.) for 12 weeks, followed by ribavirin at the same dose q.d. plus interferon-alpha (IFN-alpha) [3 million units three times a week (3 MU TIW)] for another 48 weeks. Based on an intent-to-treat analysis, the percentages of patients with undetectable HCV RNA in their serum were 0%, 38.7% and 45.2% after 12, 36 and 60 weeks of therapy, respectively. A sustained virological response, as defined by undetectable serum HCV RNA 24 weeks after the end of treatment, was observed in 9/31 patients (29%). Sustained responders had a significant improvement of their liver inflammatory activity score (P=0.025), but not of their liver fibrosis score. The chances of sustained virological response correlated with the length of treatment, but not with the HCV genotype or baseline HCV RNA level. In conclusion, patients with recurrent hepatitis C after LT might benefit from ribavirin/IFN-alpha therapy, provided that the treatment is tolerated for a sufficient duration of time.

摘要

丙型肝炎病毒(HCV)感染在肝移植(LT)后总是会复发,移植肝慢性肝炎的后遗症是发病和死亡的重要原因。在一项非对照试验中,31例肝移植后经组织学确诊为丙型肝炎的患者,先连续12周接受利巴韦林(10mg/kg体重,每日一次)治疗,随后以相同剂量每日一次的利巴韦林加α干扰素(IFN-α)[300万单位,每周三次(3MU,TIW)]再治疗48周。基于意向性分析,治疗12周、36周和60周后,血清中HCV RNA检测不到的患者百分比分别为0%、38.7%和45.2%。在31例患者中有9例(29%)观察到持续病毒学应答,定义为治疗结束后24周血清HCV RNA检测不到。持续应答者的肝脏炎症活动评分有显著改善(P=0.025),但肝脏纤维化评分没有改善。持续病毒学应答的机会与治疗时间长度相关,但与HCV基因型或基线HCV RNA水平无关。总之,肝移植后复发性丙型肝炎患者可能从利巴韦林/IFN-α治疗中获益,前提是治疗能耐受足够长的时间。

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