Xirouchakis E, Triantos C, Manousou P, Sigalas A, Calvaruso V, Corbani A, Leandro G, Patch D, Burroughs A
The Royal Free Sheila Sherlock Liver Centre, Royal Free Hospital, London, UK.
J Viral Hepat. 2008 Oct;15(10):699-709. doi: 10.1111/j.1365-2893.2008.01019.x. Epub 2008 Jul 28.
Pegylated interferon with ribavirin (Peg/R) is the most effective therapy for chronic hepatitis C virus (HCV) but its utility and effectiveness after liver transplantation has been difficult to assess. We evaluated efficacy, tolerability, and safety of Peg/R in liver transplant candidates and recipients with HCV cirrhosis. We searched medical databases and conference proceedings between January 1999 and January 2008 selecting randomized and nonrandomized studies. Primary end points meta-analytically were: (1) sustained viral response (SVR) and (2) histological response. Secondary end points were: (1) treatment discontinuation, (2) mortality, and (3) rejection episodes. Pegylated interferons using either 1-1.5 mcg/kg of pegylated interferon alpha-2b or 180 microg (pegylated interferon alpha-2a combined with ribavirin 800-1200 mg/day were the most effective compared to any other regimen or no therapy. In three pretransplant studies the median SVR was 19.6% (19.6-50%). In six postransplant studies where a meta-analysis was done the cumulative risk difference in SVR was 0.31% (95% CI, 0.18-0.44, p < 0.001). However histological response was not significantly better compared to no therapy or other antiviral regimens. There were no significant differences in discontinuation of therapy, acute or chronic rejection or mortality between optimal Peg/R vs no treatment or other regimens. Hence pegylated interferon plus ribavirin in full doses is effective pre and post transplant but has a low SVR rate. To date no significant histological improvement has been reported.
聚乙二醇干扰素联合利巴韦林(Peg/R)是治疗慢性丙型肝炎病毒(HCV)最有效的疗法,但其在肝移植后的实用性和有效性一直难以评估。我们评估了Peg/R在HCV肝硬化肝移植候选者和受者中的疗效、耐受性和安全性。我们检索了1999年1月至2008年1月期间的医学数据库和会议论文集,选择了随机和非随机研究。荟萃分析的主要终点为:(1)持续病毒学应答(SVR)和(2)组织学应答。次要终点为:(1)治疗中断、(2)死亡率和(3)排斥反应发作。与任何其他方案或不治疗相比,使用1-1.5 mcg/kg聚乙二醇干扰素α-2b或180 mcg(聚乙二醇干扰素α-2a联合利巴韦林800-1200 mg/天)的聚乙二醇干扰素最为有效。在三项移植前研究中,SVR的中位数为19.6%(19.6-50%)。在六项进行荟萃分析的移植后研究中,SVR的累积风险差异为0.31%(95%CI,0.18-0.44,p<0.001)。然而,与不治疗或其他抗病毒方案相比,组织学应答并无显著改善。在最佳Peg/R方案与不治疗或其他方案之间,治疗中断、急性或慢性排斥反应或死亡率方面无显著差异。因此,全剂量聚乙二醇干扰素加利巴韦林在移植前后均有效,但SVR率较低。迄今为止,尚未报告有显著的组织学改善。