Northwestern University Transplant Outcomes Research Collaborative (NUTORC), Comprehensive Transplant Center, Northwestern University, 676 N. St. Clair Street, 19th Floor, Chicago, IL, 60611, USA.
Medical Affairs, Americas, Astellas Pharma Global Development, Inc., 1 Astellas Way, Northbrook, IL, 60062, USA.
Adv Ther. 2019 Jun;36(6):1465-1479. doi: 10.1007/s12325-019-00904-x. Epub 2019 Apr 2.
Real-world data with extended-release tacrolimus (ER-T) are lacking in the USA. This study examined clinical outcomes and healthcare resource utilization in kidney transplant patients receiving ER-T in clinical practice.
This was a retrospective, single-center analysis (February-June 2016) using data from Northwestern University's Enterprise Data Warehouse. Adult patients receiving a kidney transplant in the preceding 4 years, treated de novo or converted to ER-T from immediate-release tacrolimus (IR-T) within 10 days post-transplantation, and maintained on ER-T (at least 3 months) were included. Patients were matched for demographic and clinical characteristics with IR-T-treated control patients. Endpoints included clinical outcomes and healthcare resource utilization up to 1 year post-transplantation.
A total of 19 ER-T-treated patients were matched with 55 IR-T-treated patients. No ER-T-treated patients experienced biopsy-confirmed acute rejection (BCAR) or graft failure versus 3 (5.5%) and 3 (5.5%) IR-T-treated patients, respectively. Mean estimated glomerular filtration rate (eGFR), the number of all-cause outpatient visits, readmissions, and all-cause hospitalization days were comparable between groups. Tacrolimus trough levels, days to target level (6-10 ng/mL), and number of required dose adjustments were also similar.
Real-world clinical outcomes and healthcare resource utilization were similar with ER-T and IR-T. Larger studies will need to investigate the trend toward fewer BCAR events, and increased graft survival with ER-T.
Astellas Pharma Global Development, Inc. Plain language summary available for this article.
美国缺乏关于延长释放他克莫司(ER-T)的真实世界数据。本研究考察了在临床实践中接受 ER-T 治疗的肾移植患者的临床结局和医疗资源利用情况。
这是一项回顾性、单中心分析(2016 年 2 月至 6 月),使用了来自西北大学企业数据仓库的数据。纳入在过去 4 年内接受肾移植、在移植后 10 天内从即时释放他克莫司(IR-T)转换为 ER-T 或开始接受 ER-T 治疗且至少维持 3 个月的成年患者。患者按人口统计学和临床特征与接受 IR-T 治疗的对照患者进行匹配。终点包括移植后 1 年内的临床结局和医疗资源利用情况。
共有 19 名接受 ER-T 治疗的患者与 55 名接受 IR-T 治疗的患者相匹配。与接受 IR-T 治疗的患者相比,没有接受 ER-T 治疗的患者发生经活检证实的急性排斥反应(BCAR)或移植物失功,分别为 0 例(0%)和 3 例(5.5%)。两组间平均估算肾小球滤过率(eGFR)、全因门诊就诊次数、再入院次数和全因住院天数相当。他克莫司谷浓度、达到目标水平(6-10ng/ml)的天数和所需剂量调整次数也相似。
真实世界中,ER-T 和 IR-T 的临床结局和医疗资源利用情况相似。需要更大规模的研究来探究 ER-T 治疗时 BCAR 事件减少和移植物存活率提高的趋势。
安斯泰来制药全球开发公司。本文提供通俗易懂的摘要。