Population pharmacokinetic modeling of treosulfan and rationale for dose recommendation in children treated for conditioning prior to allogeneic hematopoietic stem cell transplantation

被引:1
作者
Li, Xieran [1 ]
Kalwak, Krzysztof [2 ]
Beier, Rita [3 ]
Kehne, Jochen [1 ]
Moeller, Ann-Kristin [1 ]
Baumgart, Joachim [1 ]
Beelen, Dietrich W. [4 ]
Hilger, Ralf A. [5 ]
Vora, Ajay [6 ]
Sykora, Karl -Walter [3 ]
机构
[1] medac GmbH, Theaterstr 6, D-22880 Wedel, Germany
[2] Wroclaw Med Univ, Dept Pediat Hematol Oncol & Bone Marrow Transplant, Wybrzeze Ludw Pasteura 1, PL-50367 Wroclaw, Poland
[3] Hannover Med Sch, Dept Paediat Haematol & Oncol, Carl Neuberg Str 1, D-30625 Hannover, Germany
[4] Univ Hosp Essen, West German Canc Ctr, Dept Haematol & Stem Cell Transplantat, Hufelandstr 55, D-45147 Essen, Germany
[5] Univ Hosp Essen, West German Canc Ctr, Dept Med Oncol, Hufelandstr 55, D-45147 Essen, Germany
[6] Great Ormond St Hosp Children NHS Fdn, Great Ormond St, London WC1N 3JH, England
关键词
Population pharmacokinetic; Treosulfan; Children; Allogeneic hematopoietic stem cell; transplantation; PREPARATIVE REGIMEN; SURFACE-AREA; FLUDARABINE; TOXICITY; ONCOLOGY; WEIGHT; RISK; HSCT;
D O I
10.1016/j.dmpk.2023.100515
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Intravenously infused treosulfan was evaluated in adult and pediatric patients for conditioning regimen prior to allogeneic hematopoietic stem cell transplantation. A population pharmacokinetic (PK) model was initially developed on 116 adult and pediatric PK profiles from historical trials, to support treosulfan dose recommendations for children in 2 prospective trials. The aim was to assess and update the initial population PK model by inclusion of additional 83 pediatric PK profiles from these 2 trials. The final population PK model was 2-compartmental with dosing in the central compartment, linear elimination, and inter-compartmental clearance. Inter-individual variability was included on clearance (CL), central volume (V1), peripheral volume (V2), and inter-compartmental clearance (Q). The final model described an effect of the body surface area (BSA) on CL, V1, V2, and Q. The final model resulted in a modified dose recommendation for children and advises treosulfan doses of 10 g/m2, 12 g/m2, and 14 g/m2 for BSAs of <0.4 m2, & GE;0.4 to <0.9 m2, and & GE;0.9 m2, respectively. This simplified BSA-dependent dose recom-mendation was developed for children, ensuring a well comparable treosulfan exposure as a dose of 14 g/ m2 in adults -irrespective of their age and without applying individual therapeutic drug monitoring. & COPY; 2023 The Japanese Society for the Study of Xenobiotics. Published by Elsevier Ltd. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
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页数:9
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