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Evaluating the Cost-Effectiveness of Prolonged-Release Tacrolimus Relative to Immediate-Release Tacrolimus in Liver Transplant Patients Based on Data from Routine Clinical Practice

机译:基于常规临床实践数据评估肝移植患者中延长释放他克莫司相对于立即释放他克莫司的成本-效果

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Background As of 2014, there were approximately 8300 patients with a functioning liver transplant in the UK Transplant Registry, with 880 liver transplants performed in 2013–2014 alone. Tacrolimus, typically used in combination with steroids and mycophenolate mofetil, currently represents the cornerstone of post-transplant immunosuppression in liver transplant recipients. Objectives The objective of the present study was to evaluate the cost-effectiveness of prolonged-release (PR) tacrolimus (Advagraf?, Astellas Pharma Inc., Tokyo, Japan) versus branded immediate-release (IR) tacrolimus (Prograf?, Astellas Pharma Inc., Tokyo, Japan) in liver transplant recipients in the UK. Methods A model was developed in Microsoft Excel to estimate costs associated with immunosuppressive medications and retransplantation. Three-year patient and graft survival data were taken from a recent retrospective registry analysis and dose data were taken from prescribing information. Costs in 2014 pounds sterling were taken from the British National Formulary and the National Health Service National Tariff. Results Over a 3-year time horizon, the numbers needed to treat with PR tacrolimus relative to IR tacrolimus were 14 to avoid one graft loss and 18 to avoid one death. The model was sensitive to dosing assumptions, with incremental cost estimates varying between a saving of £1642 (standard deviation £885) per patient, assuming the same per-kilogram dosing of PR tacrolimus (Advagraf?) and IR tacrolimus (Prograf?) and an increase of £1350 (£964) using RCT dose data. Conclusion Data from a recent analysis of routine clinical practice data in liver transplant recipients on PR tacrolimus and IR tacrolimus showed significant differences in long-term graft survival in favor of PR tacrolimus. Modeling these data in the UK showed that, over a 3-year time horizon, one graft would be saved for every 14 patients treated with PR tacrolimus with minimal impact on costs when compared with branded IR tacrolimus (Prograf?).
机译:背景技术截至2014年,英国移植注册中心大约有8300例肝移植患者,仅2013-2014年就进行了880例肝移植。他克莫司通常与类固醇和霉酚酸酯联用,目前是肝移植受者移植后免疫抑制的基石。目的本研究的目的是评估长期释放他克莫司(PR)他克莫司(Advagraf ?,日本东京的Astellas Pharma Inc.)与品牌即刻释放(IR)的成本效益。他克莫司(Prograf ?,Astellas Pharma Inc.,日本东京)在英国的肝移植受者中。方法在Microsoft Excel中开发了一个模型,以估计与免疫抑制药物和再移植相关的费用。病人和移植物的三年生存数据来自最近的回顾性注册表分析,剂量数据来自处方信息。 2014英镑的成本来自英国国家配方奶粉和国家卫生服务局国家关税。结果在3年的时间范围内,相对于IR他克莫司,PR他克莫司治疗所需的数量为避免移植物丢失的14例和避免死亡的18例。该模型对剂量假设很敏感,假设每公斤PR他克莫司剂量(Advagraf ?)和相同的剂量(每公斤)和每位患者节省£ 1642(标准差£ 885)和增加的成本估算之间存在差异。使用RCT剂量数据,他克莫司(Prograf ?)的IR和and1350(£ 964)升高。结论从最近对肝移植接受者进行PR他克莫司和IR他克莫司的常规临床实践数据的分析得出的数据显示,支持PR他克莫司的长期移植存活率存在显着差异。在英国对这些数据进行建模显示,在3年的时间范围内,与使用IR他克莫司(Prograf ?)。

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