1. A pharmacokinetic model for voriconazole in a highly diversified population of children and adolescents with cancer.
- Author
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Carlesse, Fabianne Altruda de Moraes Costa, Araujo, Orlei Ribeiro, Silva, Dafne Cardoso Bourguignon da, Marques, Leticia Maria Acioli, Senerchia, Andreza Almeida, and Petrilli, Antonio Sergio
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CHILDHOOD cancer , *TEENAGERS , *PHARMACOKINETICS , *VORICONAZOLE , *CLINICAL trials - Abstract
Summary: Background: The wide pharmacokinetic variability of voriconazole leads to uncertainty regarding adequate exposure. Objectives: To create a pharmacokinetic model that could help to explain the variability. Methods: Retrospective review of paediatric patients with cancer. Models were built using Pmetrics. Results: We analysed 158 trough measurements in 55 patients; in 41.8%, the serum levels were between 1 and 6 mg/L on initial measurement. After the measurements, dosage adjustments were made in 42 (76.3%) patients, and the percentage of adequate levels rose to 54.5%. Fourteen deaths (25.4%) were attributed to invasive fungal diseases. The mean serum levels were higher in deceased patients (mean ± SD: 3.1 ± 3.2 mg/L vs 2.5 ± 3.6 mg/L in survivors; P = 0.018), but the median doses per kg were higher in survivors. Drug exposure was also higher in deceased patients (mean ± SD of AUC: 19.2 ± 8.1 vs 9.5 ± 19.1 in survivors; P = 0.005). No correlation was found between serum concentrations <1 mg/L and death attributable to fungal disease. Bioavailability was estimated in 50%. The maximum velocity of clearance was reduced in deceased patients. Conclusions: Extremely ill patients can be poor metabolizers of voriconazole. Therapeutic monitoring promotes only a limited improvement in drug management. [ABSTRACT FROM AUTHOR]
- Published
- 2019
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