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Evaluation of Limited Sampling Methods for Oral Busulfan Pharmacokinetic Monitoring in Adult Patients Undergoing Hematopoietic Stem Cell Transplantation

机译:成人造血干细胞移植患者口服白消安药代动力学监测有限采样方法的评价

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Background:Monitoring busulfan area under the plasma concentration-time curve (AUC) to establish the dose regimen for stem cell transplantation desirable to achieve efficacy while avoiding toxicity.Objective:Our objective was to compare AUCs calculated by 18 limited sampling methods (LSMs) from 2 to 5 samples to reference AUCs determined from 10 samples in a retrospective study of 103 adult patients receiving oral busulfan. LSMs using 2 or 3 samples were ineffective.Methods:Four LSMs using 4 or 5 blood samples that accurately characterized busulfan AUC were identified. The best 2 methods were obtained with sampling at 0.5, 1, 2, 4, and 6 hours and after 1, 1.5, 2, 4, and 6 hours postdose. For these LSMs, the incidence of 20% difference between AUCs from LSMs and reference AUCs was less than 1.3%.Conclusions:Effective and safe determination of AUC for oral busulfan can be made with strategies using only 4 or 5 concentration timepoints.
机译:背景:在血浆浓度-时间曲线(AUC)下监测白消安面积,以建立干细胞移植的剂量方案,以实现疗效并避免毒性。目的:我们的目的是比较通过18种有限采样方法(LSM)计算的AUC在对103名接受口服白消安的成年患者进行的回顾性研究中,从10个样品中确定了2至5个参考AUC样品。方法:使用2或3个样本的LSM无效。方法:鉴定4个使用4或5个血液样本的LSM,它们准确地表征了白消安AUC。获得最佳的2种方法,分别在给药后0.5、1、2、4和6小时以及给药后1、1.5、2、4和6小时取样。对于这些LSM,LSM与参考AUC之间的AUC发生率相差20%的发生率小于1.3%。结论:仅使用4个或5个浓度时间点的策略可以有效,安全地测定口服白消安的AUC。

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