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接受造血干细胞移植儿童的静脉注射白消安剂量个体化:有限采样策略

IV busulfan dose individualization in children undergoing hematopoietic stem cell transplant: limited sampling strategies.

作者信息

Dupuis L Lee, Sibbald Cathryn, Schechter Tal, Ansari Marc, Gassas Adam, Théorêt Yves, Kassir Nastya, Champagne Martin A, Doyle John

机构信息

Leslie Dan Faculty of Pharmacy, University of Toronto, Toronto, Ontario, Canada.

出版信息

Biol Blood Marrow Transplant. 2008 May;14(5):576-82. doi: 10.1016/j.bbmt.2008.03.002.

Abstract

We currently calculate area under the busulfan concentration time curve (AUC) using 7 plasma busulfan concentrations (AUC7) drawn after the first of 16 i.v. busulfan doses given as a 2-hour infusion every 6 hours. The aim of this study was to develop and validate limited sampling strategies (LSSs) using 3 or fewer busulfan concentration values with which to reliably calculate AUC in children undergoing hematopoietic stem cell transplant (HSCT). Children in the development group (44) received i.v. busulfan at Sick Kids; the validation group consisted of 35 children who received care at CHU Ste-Justine. Busulfan doses given and subsequent plasma busulfan concentrations were recorded. LSSs using 1 to 3 concentration-time points were developed using multiple linear regression. LSS were considered to be acceptable when adjusted r(2) > 0.9, mean bias <15% and precision <15%. Extent of agreement between the AUC7 values and the LSS AUC was assessed by the intraclass correlation coefficient (ICC) and Bland-Altman (BA) analysis. Agreement was considered to be excellent when the lower limit of the 95% confidence limit of the ICC exceeded 0.9 and when the limits of agreement in the BA analysis were +/-15% for both AUC and dose. Administration of the theoretic adjusted busulfan doses based on each LSS was simulated and cases where the resulting AUC was >1500 or <900 microM x min were noted. LSSs using 1, 2, or 3 plasma busulfan concentrations were developed that showed excellent agreement with AUC7 and adjusted busulfan doses. In the validation sample, only the 2- and 3-point LSSs demonstrated acceptable precision and lack of bias. LSSs using 2 or 3 plasma busulfan concentrations can be used to reliably estimate busulfan AUC after IV administration in children undergoing HSCT.

摘要

我们目前使用在16次静脉注射白消安剂量中的首次剂量(每6小时进行2小时输注)后采集的7个血浆白消安浓度来计算白消安浓度-时间曲线下面积(AUC)(AUC7)。本研究的目的是开发并验证有限采样策略(LSS),该策略使用3个或更少的白消安浓度值来可靠地计算接受造血干细胞移植(HSCT)的儿童的AUC。开发组的44名儿童在病童医院接受静脉注射白消安治疗;验证组由35名在圣贾斯汀大学医疗中心接受治疗的儿童组成。记录给予的白消安剂量及随后的血浆白消安浓度。使用多元线性回归开发了使用1至3个浓度-时间点的LSS。当调整后的r²>0.9、平均偏差<15%且精密度<15%时,LSS被认为是可接受的。通过组内相关系数(ICC)和布兰德-奥特曼(BA)分析评估AUC7值与LSS AUC之间的一致性程度。当ICC的95%置信限下限超过0.9且BA分析中AUC和剂量的一致性界限均为±15%时,一致性被认为是极好的。模拟了基于每个LSS给予理论调整后的白消安剂量的情况,并记录了所得AUC>1500或<900μM·min的情况。开发了使用1、2或3个血浆白消安浓度的LSS,其与AUC7和调整后的白消安剂量显示出极好的一致性。在验证样本中,只有2点和3点LSS显示出可接受的精密度且无偏差。使用2或3个血浆白消安浓度的LSS可用于可靠地估计接受HSCT的儿童静脉注射后白消安的AUC。

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