首页> 外文期刊>Transplantation Proceedings >Safety and efficacy of conversion from twice-daily tacrolimus (Prograf) to once-daily prolonged-release tacrolimus (Graceptor) in stable kidney transplant recipients
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Safety and efficacy of conversion from twice-daily tacrolimus (Prograf) to once-daily prolonged-release tacrolimus (Graceptor) in stable kidney transplant recipients

机译:在稳定的肾脏移植受者中从每日两次他克莫司(Prograf)转换为每天一次长时间释放他克莫司(Graceptor)的安全性和有效性

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Background: Graceptor is a new modified-release once-daily formulation of tacrolimus with an efficacy and safety profile similar to twice-daily tacrolimus (Prograf), as identified by clinical trials, offering a more convenient dosing regimen to improve adherence. The aim of this study was to analyze the safety of a 1:1 dose conversion from twice-daily Prograf to once-daily Graceptor in stable kidney transplant recipients. Methods: We switched 33 Japanese patients who had undergone kidney transplantation ≥1 years before from twice-daily Prograf to once-daily Graceptor. The dose conversion ratio between Prograf and Graceptor was 1:1. We compared the following parameters: minimum tacrolimus concentration (C min); concentration dose per weight (CDW); serum creatinine (sCr); blood urea nitrogen (BUN); total cholesterol (TC); high-density lipoprotein cholesterol (HDL-C); uric acid (UA); fasting blood sugar (FBS). Time points for measurements were 1 month before study start and 1 and 2 months afterward. Results: The mean age of the subjects in this study was 46.5 ± 13.1 years. Mean C min decreased from 4.55 ± 1.79 to 3.20 ± 1.22 ng/dL. The mean CDW also decreased, from 99.8 ± 69.5 to 75.0 ± 55.1 mg/dL/kg over the 2 months. There were no significant changes in sCR, BUN, UA, and FBS. Mean TC increased from 187.5 ± 51.4 to 194.3 ± 43.4 mg/dL, and mean HDL-C changed from 53.7 ± 12.0 to 56.1 ± 11 mg/dL. There were no episodes of rejection or infection. Conclusions: We conclude that switching from Prograf to Graceptor is safe and has the advantage of improving adherence. It could also have a beneficial effect in controlling glycemic levels and the adverse effects of tacrolimus. In many cases (25%30%), the minimum concentration of tacrolimus decreased after changing tablets. With Graceptor, the ratio of area under trough level to area under the curve (AUC) is low compared with Prograf, resulting in low C min values of 12 ng/mL, and the AUC for Graceptor is very similar to that for Prograf.
机译:背景:Graceptor是他克莫司的新型改良释放每日一次制剂,其功效和安全性与临床试验所确定的每天两次他克莫司(Prograf)相似,提供了一种更方便的给药方案来改善依从性。这项研究的目的是分析稳定肾脏移植受者中从每天两次的Prograf到每天一次的Graceptor 1:1剂量转换的安全性。方法:我们将33例≥1年以前接受肾脏移植的日本患者从每天两次Prograf改为每天一次Graceptor。 Prograf和Graceptor之间的剂量转化率为1:1。我们比较了以下参数:他克莫司的最低浓度(C min);每重量浓度剂量(CDW);血清肌酐(sCr);血液尿素氮(BUN);总胆固醇(TC);高密度脂蛋白胆固醇(HDL-C);尿酸(UA);空腹血糖(FBS)。测量的时间点是研究开始前1个月,之后1和2个月。结果:本研究受试者的平均年龄为46.5±13.1岁。平均C min从4.55±1.79降至3.20±1.22 ng / dL。在两个月内,平均CDW也从99.8±69.5降至75.0±55.1 mg / dL / kg。 sCR,BUN,UA和FBS没有明显变化。平均TC从187.5±51.4增至194.3±43.4 mg / dL,平均HDL-C从53.7±12.0增至56.1±11 mg / dL。没有排斥或感染的发作。结论:我们得出结论,从Prograf转换为Graceptor是安全的,并且具有提高依从性的优势。它还可能在控制血糖水平和他克莫司的不利影响方面具有有益作用。在许多情况下(25%30%),他克莫司的最低浓度在更换片剂后降低。与Prograf相比,使用Graceptor时,槽下面积与曲线下面积(AUC)的比率较低,导致C min值低至12 ng / mL,并且Graceptor的AUC与Prograf非常相似。

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