Back to Search Start Over

Evaluation of treosulfan cumulative exposure in paediatric patients through population pharmacokinetics and dosing simulations.

Authors :
Rosser SPA
Lee S
Kohli S
Keogh SJ
Chung J
O'Brien T
Fraser C
McLachlan AJ
Shaw PJ
Nath CE
Source :
British journal of clinical pharmacology [Br J Clin Pharmacol] 2023 Apr; Vol. 89 (4), pp. 1413-1424. Date of Electronic Publication: 2022 Nov 28.
Publication Year :
2023

Abstract

Aim: To investigate the pharmacokinetics (PK) of intravenous treosulfan in paediatric patients undergoing haematopoietic stem cell transplantation (HSCT) for a broad range of diseases and to explore the impact of different dosing regimens on treosulfan exposure (area under the concentration-time curve, AUC <subscript>0→∞</subscript> ) through dosing simulations.<br />Methods: A prospective multicentre PK study was conducted using treosulfan concentration data (n = 423) collected from 53 children (median age 3.5, range 0.2-17.0 years) receiving three daily age-guided doses (10-14 g/m <superscript>2</superscript> ). Population PK modelling was performed using NONMEM software, utilising a stepwise forward selection backward elimination method and likelihood-ratio test for screening covariates to describe PK variability. Monte Carlo simulation was used to generate patient PK data for 10 000 virtual paediatric patients and cumulative AUC <subscript>0→∞</subscript> values were evaluated using age, body surface area (BSA) and model-based dosing regimens, targeting 4800 mg*h/L.<br />Results: Treosulfan concentration data were described using a one-compartment PK model with first-order elimination. Population mean (95% CI) estimates for clearance (CL) and volume of distribution (V) were 16.3 (14.9-18.1) L/h and 41.9 (38.8-45.1) L, respectively. Allometrically scaled body weight was the best covariate descriptor for CL and V, and maturational age further explained variability in CL. Dosing simulations indicated that in young patient groups (<2 years), a model-based dosing regimen more accurately achieved the target AUC <subscript>0→∞</subscript> (58.3%) over the age (42.6%) and BSA-based (51.3%) regimens.<br />Conclusion: Treosulfan disposition was described through allometric body weight and maturational age descriptors. Model-informed dosing is recommended for patients under 2 years. Treosulfan PK parameters and AUC <subscript>0→∞</subscript> were not influenced by patient disease.<br /> (© 2022 The Authors. British Journal of Clinical Pharmacology published by John Wiley & Sons Ltd on behalf of British Pharmacological Society.)

Details

Language :
English
ISSN :
1365-2125
Volume :
89
Issue :
4
Database :
MEDLINE
Journal :
British journal of clinical pharmacology
Publication Type :
Academic Journal
Accession number :
36369677
Full Text :
https://doi.org/10.1111/bcp.15599