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患者特征是否会影响接受依维莫司治疗的肝移植患者的疗效和肾脏预后?

Do patient characteristics influence efficacy and renal outcomes in liver transplant patients receiving everolimus?

作者信息

De Simone Paolo, Saliba Faouzi, Dong Gaohong, Escrig Cesar, Fischer Lutz

机构信息

Hepatobiliary Surgery and Liver Transplantation, Azienda Ospedaliero-Universitaria Pisana, Pisa, Italy.

Hepatobiliary Center, AP-HP Hôpital Paul Brousse, Université Paris-Sud, Villejuif, France.

出版信息

Clin Transplant. 2016 Mar;30(3):279-88. doi: 10.1111/ctr.12687. Epub 2016 Feb 6.

Abstract

Data from the 24-month randomized, multicenter, open-label H2304 study in 719 de novo liver transplant recipients were analyzed to evaluate the influence of variables potentially affecting immunological or renal response: recipient age, gender, end-stage disease, hepatitis C virus (HCV) status, and Model for End-stage Liver Disease score and estimated glomerular filtration rate (eGFR) at randomization (day 30). Treated BPAR was similar between everolimus with reduced tacrolimus (EVR + Reduced TAC) vs. conventional tacrolimus-based therapy (TAC Control) in all subpopulations, with a trend to lower risk under everolimus with reduced tacrolimus (EVR + Reduced TAC) in patients < 60 yrs and HCV-negative recipients. Risk of graft loss or death was similar in both treatment groups for all subpopulations. The change in eGFR to month 24 showed a benefit for EVR + Reduced TAC vs. TAC Control in all subpopulations other than those with the lowest baseline eGFR (30 to < 55 mL/min/1.73 m(2)), with a significant difference in favor of EVR + Reduced TAC for younger recipients (< 60 yr), female patients, HCV-negative patients and those with baseline eGFR of 55 to < 70 mL/min/1.73 m(2). Everolimus with reduced tacrolimus maintains efficacy to at least two yr after liver transplantation even in patients with risk factors for rejection, with particular renal benefits in specific patient subpopulations.

摘要

对719例初发肝移植受者进行的为期24个月的随机、多中心、开放标签H2304研究数据进行分析,以评估可能影响免疫或肾脏反应的变量的影响:受者年龄、性别、终末期疾病、丙型肝炎病毒(HCV)状态、终末期肝病模型评分以及随机分组时(第30天)的估计肾小球滤过率(eGFR)。在所有亚组中,与基于传统他克莫司的治疗(TAC对照)相比,他克莫司减量的依维莫司(EVR + 减量TAC)治疗的BPAR相似,在<60岁的患者和HCV阴性受者中,他克莫司减量的依维莫司(EVR + 减量TAC)有风险降低的趋势。两个治疗组在所有亚组中的移植物丢失或死亡风险相似。至第24个月时eGFR的变化显示,除基线eGFR最低(30至<55 mL/min/1.73 m²)的亚组外,EVR + 减量TAC组相对于TAC对照组有获益,在年轻受者(<60岁)、女性患者、HCV阴性患者以及基线eGFR为55至<70 mL/min/1.73 m²的患者中,EVR + 减量TAC组有显著优势。他克莫司减量的依维莫司在肝移植后至少两年内保持疗效,即使在有排斥反应危险因素的患者中也是如此,在特定患者亚组中对肾脏有特别益处。

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