Burra P, Targhetta S, Pevere S, Boninsegna S, Guido M, Canova D, Brolese A, Masier A, D'Aloiso C, Germani G, Tomat S, Fagiuoli S
Department of Surgical and Gastroenterological Sciences, University Hospital, Padova, Italy.
Transplant Proc. 2006 May;38(4):1127-30. doi: 10.1016/j.transproceed.2006.02.135.
Hepatitis C virus (HCV) reinfection after liver transplantation is a virtually constant finding and leads to chronic hepatitis and cirrhosis in variable proportions. This study aimed to assess the safety and efficacy of alpha-interferon (IFN) plus ribavirin for recurrent HCV following liver transplantation.
Thirty of 55 patients (54.5%) with histologically proven HCV recurrence after liver transplantation were given antiviral therapy (alpha-IFN at a dose of 6 MU x 3 x week IM associated with oral ribavirin 1 g/d for 12 months) and followed up for a further 12 months after the end of the treatment. Liver and renal function tests, hemocytometric values, and HCV-RNA were assessed every 3 months throughout the therapy and follow-up. Liver biopsy was performed before and after the treatment and after another 12 months of follow-up.
Eight patients (26.7%) were withdrawn from the treatment due to adverse events and another 8 (26.7%) needed a dosage reduction. Eleven patients (36.7%) had a biochemical and virological response, becoming aminotransferase and HCV-RNA negative at the end of the treatment; 6 patients (20%) still had a sustained response after 12 months of follow-up. All 6 patients are clinically stable at 6 years after completing the antiviral therapy. A low viral load before therapy was a positive predictor of sustained response. No histologically significant improvement was seen at the end of the therapy or after the follow-up.
The combination of alpha-IFN plus ribavirin induced a sustained virologic response in 20% of liver transplant recipients with recurrent HCV, but intolerance of the therapy prompted its discontinuation or a dosage reduction in a large proportion of patients. However, we have observed a long-term efficacy of the antiviral therapy in the sustained responders.
肝移植后丙型肝炎病毒(HCV)再感染几乎是一个常见现象,并会不同程度地导致慢性肝炎和肝硬化。本研究旨在评估α干扰素(IFN)联合利巴韦林治疗肝移植后复发性HCV的安全性和疗效。
55例肝移植后经组织学证实HCV复发的患者中,30例(54.5%)接受了抗病毒治疗(α-IFN剂量为6 MU,每周3次,肌肉注射,联合口服利巴韦林1 g/d,共12个月),并在治疗结束后进一步随访12个月。在整个治疗和随访过程中,每3个月评估一次肝功能和肾功能、血细胞计数以及HCV-RNA。在治疗前后以及随访12个月后进行肝活检。
8例患者(26.7%)因不良事件退出治疗,另外8例(26.7%)需要减少剂量。11例患者(36.7%)出现生化和病毒学应答,在治疗结束时转氨酶和HCV-RNA转为阴性;6例患者(20%)在随访12个月后仍有持续应答。所有6例患者在完成抗病毒治疗6年后临床稳定。治疗前病毒载量低是持续应答的一个阳性预测指标。在治疗结束时或随访后,未观察到组织学上的显著改善。
α-IFN联合利巴韦林治疗使20%的肝移植复发性HCV患者获得了持续病毒学应答,但该治疗的不耐受性促使大部分患者停药或减少剂量。然而,我们观察到抗病毒治疗对持续应答者具有长期疗效。