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

Cyclosporine versus tacrolimus treated liver transplant recipients with chronic hepatitis C: outcomes analysis of the UNOS/OPTN database.

机构信息

Health Outcomes Research and Biostatistics, CTI Clinical Trial and Consulting Services, Raleigh, NC, USA.

出版信息

Am J Transplant. 2011 Aug;11(8):1676-85. doi: 10.1111/j.1600-6143.2011.03508.x. Epub 2011 May 12.

DOI:10.1111/j.1600-6143.2011.03508.x
PMID:21564522
Abstract

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.

摘要

慢性丙型肝炎病毒 (HCV) 复发仍然是肝移植患者发病率和死亡率的一个问题。包括钙调神经磷酸酶抑制剂在内的免疫抑制剂已被认为可加速 HCV 的复发。最近的研究表明,与他克莫司 (TAC) 相比,环孢素 (CSA-ME) 的结果可能更好,但数据尚无定论。我们回顾性分析了来自美国器官共享网络的 8809 例慢性 HCV 肝移植受者的数据,这些受者在出院前接受环孢素微乳剂 (CSA-ME) 或他克莫司 (TAC) 作为维持性免疫抑制治疗。我们分析了 CSA-ME 与 TAC 治疗患者的患者死亡、移植物失败、因复发疾病和急性细胞排斥 (ACR) 导致的失败。CSA-ME 组 3 年未调整的患者和移植物存活率分别为 76.8%和 71.5%,TAC 组分别为 79.9%和 75.0%。倾向评分调整后的结果表明,CSA-ME 治疗患者的患者死亡和移植物失败风险增加[风险比 (HR) = 1.17;95%CI = 1.01-1.36 和 HR = 1.19;95%CI = 1.04-1.35],活检证实的 AR (HR = 2.03;95%CI = 1.54-2.67) 与 TAC 治疗患者相比。这些结果为重新考虑将 CSA-ME 靶向用于 HCV 感染的肝移植受者提供了证据。

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