Fernández Inmaculada, Meneu Juan Carlos, Colina Francisco, García Ignacio, Muñoz Raquel, Castellano Gregorio, Fuertes Antonio, Abradelo Manuel, Lumbreras Carlos, Moreno Enrique, Solís-Herruzo José Antonio
Gastroenterology Department, Hospital Universitario "12 de Octubre," Madrid, Spain.
Liver Transpl. 2006 Dec;12(12):1805-12. doi: 10.1002/lt.20883.
Treatment of recurrent hepatitis C in liver transplant is controversial. The aim of our study was to evaluate the clinical and histological efficacy of pegylated interferon alpha 2b (PEG-IFN) and ribavirin therapy of recurrent hepatitis C after liver transplantation (LT). We prospectively included 47 liver transplant patients with: 1) a positive test for hepatitis C virus (HCV)-ribonucleic acid (RNA) in serum; 2) alanine aminotransferase (ALT) >45 UI/mL; and 3) a liver biopsy showing chronic hepatitis without rejection in the previous 2 months. Patients received PEG-IFN (1.5 microg/kg/week) and ribavirin (800-1,000 mg/day) for 12 months. Follow-up was based on biochemical (ALT), virological (RNA-HCV), and histological (liver biopsy) examinations. Follow-up lasted a minimum of 6 months after the end of antiviral therapy. Sustained virological response (SVR) was achieved in 23% of the patients. A total of 33 (70%) patients had normalized ALT levels at the end of therapy. Inflammatory portal and lobular score declined significantly in patients with SVR (P < 0.05) but not in nonresponder patients. Fibrosis did not change significantly in either group. SVR was significantly associated with low gamma-glutamyltransferase GGT (P = 0.04) and HCV-RNA levels (P = 0.03), a virological response at 12 weeks (P = 0.002) and patient's compliance (P = 0.04). Ten (21%) patients were withdrawn prematurely due to adverse effects. In conclusion, Therapy with PEG-IFN and ribavirin achieved SVR and a significant histological improvement in 23% of liver transplant recipients with chronic hepatitis C. Toxicity is an important drawback of this therapy.
肝移植后复发性丙型肝炎的治疗存在争议。我们研究的目的是评估聚乙二醇化干扰素α-2b(PEG-IFN)联合利巴韦林治疗肝移植(LT)后复发性丙型肝炎的临床和组织学疗效。我们前瞻性纳入了47例肝移植患者,这些患者满足以下条件:1)血清丙型肝炎病毒(HCV)核糖核酸(RNA)检测呈阳性;2)丙氨酸氨基转移酶(ALT)>45 UI/mL;3)肝活检显示在过去2个月内为慢性肝炎且无排斥反应。患者接受PEG-IFN(1.5μg/kg/周)和利巴韦林(800 - 1000 mg/天)治疗12个月。随访基于生化检查(ALT)、病毒学检查(RNA-HCV)和组织学检查(肝活检)。抗病毒治疗结束后随访至少持续6个月。23%的患者实现了持续病毒学应答(SVR)。共有33例(70%)患者在治疗结束时ALT水平恢复正常。SVR患者的炎症门静脉和小叶评分显著下降(P < 0.05),而无应答患者则无明显下降。两组患者的纤维化程度均无显著变化。SVR与低γ-谷氨酰转移酶GGT(P = 0.04)、HCV-RNA水平(P = 0.03)、12周时的病毒学应答(P = 0.002)以及患者的依从性(P = 0.04)显著相关。10例(21%)患者因不良反应提前停药。总之,PEG-IFN联合利巴韦林治疗使23%的慢性丙型肝炎肝移植受者实现了SVR并取得了显著的组织学改善。毒性是该治疗方法的一个重要缺点。