Busulfan Exposure Target Attainment in Adults Undergoing Allogeneic Hematopoietic Cell Transplantation: A Single Day Versus a Multiple Day Therapeutic Drug Monitoring Regimen

被引:2
作者
Bognar, T. [1 ]
Bartelink, I. H. [2 ,3 ]
van der Elst, K. C. M. [1 ]
Kingma, J. S. [1 ,4 ]
Smeijsters, E. H. [1 ]
Lindemans, C. A. [5 ,6 ]
Egberts, A. C. G. [1 ,7 ]
Kuball, J. H. E. [8 ,9 ]
de Witte, M. A. [8 ,9 ]
Schultink, A. H. M. de Vries [1 ]
Lalmohamed, A. [1 ,7 ]
机构
[1] Univ Med Ctr Utrecht, Wilhelmina Childrens Hosp, Dept Clin Pharm, Utrecht, Netherlands
[2] Univ Amsterdam, Vrije Univ Amsterdam, Pharm & Clin Pharmacol, Med Ctr, Amsterdam, Netherlands
[3] Canc Ctr Amsterdam, Amsterdam, Netherlands
[4] St Antonius Hosp, Dept Clin Pharm, Nieuwegein, Netherlands
[5] Princess Maxima Ctr Pediat Oncol, Utrecht, Netherlands
[6] Univ Med Ctr Utrecht, Wilhelmina Childrens Hosp, Dept Pediat, Utrecht, Netherlands
[7] Univ Utrecht, Utrecht Inst Pharmaceut Sci, Div Pharmacoepidemiol & Clin Pharmacol, Utrecht, Netherlands
[8] Univ Utrecht, Univ Med Ctr Utrecht, Dept Hematol, Utrecht, Netherlands
[9] Univ Utrecht, Univ Med Ctr Utrecht, Lab Translat Immunol, Utrecht, Netherlands
来源
TRANSPLANTATION AND CELLULAR THERAPY | 2024年 / 30卷 / 10期
关键词
Therapeutic drug; monitoring; Busulfan; Hematopoietic cell; transplantation; GLUTATHIONE; PHARMACOKINETICS; TOXICITY; CHILDREN; AGE;
D O I
10.1016/j.jtct.2024.07.015
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Busulfan exposure has previously been linked to clinical outcomes, hence the need for therapeutic drug monitoring (TDM). Study objective was to evaluate the effect of day 1 TDM-guided dosing (regimen d1) versus days 1 + 2 TDM-guided dosing (regimen d1 + 2) on attaining adequate busulfan exposure. In this observational study, we included all adults who received an allogeneic HCT with intravenous once daily busulfan over 4 days as part of the conditioning regimen at the University Medical Centre Utrecht or between July 31, 2014 and November 12, 2021. The primary outcome was attainment of the therapeutic busulfan target (cumulative area under the curve [AUC(cum)] 80-100 mg*h/L). Dose adjustment was based on the estimated AUC of the preceding dosing day(s). Additional TDM was performed in the event of large dose adjustments (>= 25%). The choice of TDM regimen was solely based on the first day the busulfan dose was administered (regimen d1 + 2 occurred when conditioning started on a Saturday). In all patients, blood sampling was performed on day 4 for evaluation. The AUC(cum) was estimated using a validated population pharmacokinetic model. Busulfan target exposure was compared between both TDM regimen groups using a propensity score adjusted logistic regression model. The variance in the AUC(cum) between the TDM regimens was compared using the F-test. Patients were stratified for age (categorical). In regimen d1, 87.6% (n = 113/129) attained a therapeutic busulfan exposure, while in regimen d1 + 2 a proportion of 97.4% was found (n = 74/76, adjusted odds ratio for non-therapeutic AUC = 0.19, 95% confidence interval [95% CI]: 0.04-0.89). Variance of busulfan exposure in the regimen d1 group (SD = 6.8 mg*h/L) differed significantly from the variance in the regimen d1 + 2 group (SD = 3.6 mg*h/L, F-test, P < .001). Performing busulfan TDM on both day 1 and day 2, rather than only on day 1, improves busulfan target exposure attainment in adults undergoing HCT, provided that subsequent TDM is carried out if required. (c) 2024 The American Society for Transplantation and Cellular Therapy. Published by Elsevier Inc. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/)
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收藏
页码:1007e1 / 1007e10
页数:10
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