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首页> 外文期刊>American Journal of Transplantation >Cyclosporine versus Tacrolimus Treated Liver Transplant Recipients with Chronic Hepatitis C: Outcomes Analysis of the UNOS/OPTN Database
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Cyclosporine versus Tacrolimus Treated Liver Transplant Recipients with Chronic Hepatitis C: Outcomes Analysis of the UNOS/OPTN Database

机译:环孢素与他克莫司治疗的慢性丙型肝炎肝移植受者:UNOS / OPTN数据库的结果分析

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摘要

Recurrent hepatitis C virus (HCV) remains a problematic cause of morbidity and mortality for liver transplant patients. Immunosuppression including calcineurin-inhibitors has been implicated in the acceleration of recurrent HCV. Recent studies suggest that outcomes may be better with cyclosporine (CSA-ME) compared to tacrolimus (TAC), but the data are inconclusive. We retrospectively analyzed data received from the United Network for Organ Sharing on 8809 chronic HCV liver transplant recipients receiving either cyclosporine microemulsion (CSA-ME) or tacrolimus (TAC) as maintenance immunosuppression prior to discharge. We analyzed patient death, graft failure, failure due recurrent disease and acute cellular rejection (ACR) for CSA-ME versus TAC treated patients. Three-year unadjusted patient and graft survival rates were 76.8% and 71.5%, respectively, in the CSA-ME group versus 79.9% and 75.0% in the TAC group. Propensity score-adjusted results suggest CSA-ME treated patients are at increased risk of patient death and graft failure [Hazards ratio (HR) = 1.17; 95% CI = 1.01–1.36 and HR = 1.19; 95% CI = 1.04–1.35, respectively] and biopsy-confirmed AR (HR = 2.03; 95% CI = 1.54–2.67) compared to TAC treated patients. These results provide evidence to reconsider the targeted administration of CSA-ME to HCV-infected liver transplant recipients.
机译:丙型肝炎病毒(HCV)复发仍然是肝移植患者发病和死亡的一个令人困扰的原因。包括钙调神经磷酸酶抑制剂在内的免疫抑制作用与复发性HCV的加速有关。最近的研究表明,与他克莫司(TAC)相比,环孢素(CSA-ME)的疗效可能更好,但数据尚无定论。我们回顾性分析了从8890例慢性HCV肝移植受者接受联合器官共享联合网络的数据,这些接受者在出院前接受环孢素微乳(CSA-ME)或他克莫司(TAC)作为维持性免疫抑制。我们分析了CSA-ME与TAC治疗的患者的死亡,移植失败,复发性疾病失败和急性细胞排斥(ACR)。 CSA-ME组三年未调整患者和移植物存活率分别为76.8%和71.5%,而TAC组为79.9%和75.0%。倾向得分调整后的结果表明,经CSA-ME治疗的患者死亡和移植失败的风险增加[危险比(HR)= 1.17; 95%CI = 1.01-1.36,HR = 1.19;与接受TAC治疗的患者相比,分别有95%CI = 1.04–1.35]和活检证实的AR(HR = 2.03; 95%CI = 1.54–2.67)。这些结果提供了证据,可以重新考虑对感染了HCV的肝移植受者的CSA-ME靶向给药。

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