Optimal dosing regimen of caspofungin in adolescents with allogeneic haematopoietic stem cell transplantation

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Abstract

Objectives: The optimal dosing regimen of caspofungin in adolescents undergoing allogeneic haematopoietic stem cell transplantation against Candida spp. is unknown. The study aimed to compare body surface area (BSA)-based and fixed dosing regimens through population pharmacokinetic (PPK) analysis and to optimize dosing regimens likely to achieve therapeutic exposures. Methods: Opportunistic sampling was used to collect plasma concentrations through a prospective observational pharmacokinetic study. PPK analysis and Monte Carlo simulations (n= 1000) were performed using NONMEM. Results: A total of 86 samples of 30 adolescents (12–17 years old) were best described by a two-compartment pharmacokinetic model. BSA is the only covariate on clearance and central volume of distribution. For Candida glabrata and Candida albicans, a standard dosing regimen could achieve at least a 90% probability of target attainment for the indicator of AUC0–24/MIC90. Dosing regimen simulations identified a BSA cut-off value of 1.3 m2, where a fixed loading dose (LD) is preferred when BSA ≥ 1.3 m2 and a BSA-based LD is preferred when BSA < 1.3 m2. For maintenance dose (MD), however, the BSA-based dose was proposed, regardless of BSA. The current maximum dosing regimen of LD 70 mg/day and MD 70 mg/day could not result in sufficient antifungal exposure for Candida parapsilosis with MIC90 of 1 mg/L. Furthermore, an LD of 70 mg/day and MD of 60 mg/m2/day rendered 90.4% steady-state trough concentration (Ctrough) over 1 mg/L in the virtual population. Conclusions: Our study proposed optimized dosing regimens of caspofungin based on AUC0–24/MIC90 or Ctrough, which may support further individualized treatment.

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APA

Du, B., Zhang, W., Wang, Y., Wu, Y. E., Zhang, Y. H., Anker, J. van den, … Zhao, W. (2024). Optimal dosing regimen of caspofungin in adolescents with allogeneic haematopoietic stem cell transplantation. Journal of Antimicrobial Chemotherapy, 79(10), 2678–2687. https://doi.org/10.1093/jac/dkae276

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