Prediction of Area under the Cyclosporine Concentration Versus Time Curve in Children Undergoing Hematopoietic Stem Cell Transplantation

被引:11
作者
Dupuis, L. Lee [1 ,2 ,3 ,4 ]
Seto, Winnie [1 ,4 ]
Teuffel, Oliver [2 ]
Gibson, Paul [7 ]
Schultz, Kirk R. [8 ]
Doyle, John D. [2 ,5 ]
Gassas, Adam [2 ,5 ]
Egeler, R. Maarten [2 ,3 ,5 ]
Sung, Lillian [2 ,3 ,6 ]
Schechter, Tal [2 ,3 ,6 ]
机构
[1] SickKids, Dept Pharm, Toronto, ON M5M 1X3, Canada
[2] SickKids, Div Haematol Oncol, Toronto, ON M5M 1X3, Canada
[3] SickKids, Res Inst, Toronto, ON M5M 1X3, Canada
[4] Univ Toronto, Leslie Dan Fac Pharm, Toronto, ON, Canada
[5] Univ Toronto, Fac Med, Toronto, ON, Canada
[6] Univ Toronto, Dept Paediat, Toronto, ON M5S 1A1, Canada
[7] Childrens Hosp, London Hlth Sci Ctr, London, ON, Canada
[8] Univ British Columbia, BC Childrens Hosp, Div Pediat Hematol Oncol BMT, Vancouver, BC V5Z 1M9, Canada
基金
加拿大健康研究院;
关键词
Cyclosporine; Pediatrics; Pharmacokinetics; Area under the curve; Acute graft versus host disease; VERSUS-HOST-DISEASE; BONE-MARROW-TRANSPLANTATION; ACUTE GVHD; BLOOD; PHARMACOKINETICS; FLUCONAZOLE; VALIDATION; INFUSION; EXPOSURE; LEVEL;
D O I
10.1016/j.bbmt.2012.10.031
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
This prospective study aimed to validate a previously developed first-dose limited sampling strategy (LSS) to predict the area under the cyclosporine concentration-versus-time curve (AUC) and to develop and then validate an LSS to predict cyclosporine AUC at steady state. This two-center Canadian study included children (ages .4 to 17.2 years) undergoing myeloablative allogeneic hematopoietic stem cell transplantation receiving cyclosporine for acute graft-versus-host disease prophylaxis. There were three cohorts, each incorporating 24 AUC determinations: first-dose LSS validation, steady-state LSS development, and steady-state LSS validation. Patients contributing data to either of the development cohorts were excluded from the corresponding validation group. Cyclosporine was given every 12 hours as a 2-hour infusion. Cyclosporine AUC was determined after administration of the first cyclosporine dose (8 samples) and then once weekly (9 samples) until engraftment. Steady-state LSSs were developed using stepwise multiple linear regression. An LSS was considered to provide an acceptable estimate of AUC if the lower limit of the 95% confidence limit (CL) of the intraclass coefficient was .8 or higher and both bias and precision were 15% or less. Fifty-three children age .4 to 18 years participated. Cyclosporine concentrations drawn up to 4 hours from the start of the infusion correlated most strongly with AUC. The previously developed first-dose LSSs and three steady-state LSSs met criteria for acceptability. The intraclass coefficients of the three-point first-dose LSS validation cohort, three-point steady-state LSS development cohort, and three-point steady-state LSS validation cohort were .974 (95% CL: .941 to .988), .984 (95% CL: .965 to .993), and .993 (95% CL:.984 to .997), respectively. The three-point first-dose (2, 6, and 8 hours) and steady-state (2, 2.5, and 8 hours) LSSs are valid measures of cyclosporine AUC after intravenous administration over 2 hours. Their use in a prospective evaluation of the relationship between cyclosporine AUC and hematopoietic stem cell transplantation clinical outcomes in children is suggested. (C) 2013 American Society for Blood and Marrow Transplantation.
引用
收藏
页码:418 / 423
页数:6
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