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Population Pharmacokinetics of Melphalan for Pediatric Patients Undergoing Hematopoietic Cell Transplantation.
Li, Shuhui; Dvorak, Christopher C; Lu, Ying; Chan, Danna; Gobburu, Jogarao V S; Long-Boyle, Janel; Apsel Winger, Beth.
Affiliation
  • Li S; Center for Translational Medicine, School of Pharmacy, University of Maryland, Baltimore, Maryland, USA.
  • Dvorak CC; Department of Pediatrics, Division of Allergy, Immunology, and Bone Marrow Transplantation, University of California San Francisco, San Francisco, California, USA.
  • Lu Y; Department of Pediatrics, Division of Allergy, Immunology, and Bone Marrow Transplantation, University of California San Francisco, San Francisco, California, USA.
  • Chan D; Department of Pediatrics, Division of Allergy, Immunology, and Bone Marrow Transplantation, University of California San Francisco, San Francisco, California, USA.
  • Gobburu JVS; ASTEX Pharmaceuticals, Pleasanton, California, USA.
  • Long-Boyle J; Center for Translational Medicine, School of Pharmacy, University of Maryland, Baltimore, Maryland, USA.
  • Apsel Winger B; Department of Pediatrics, Division of Allergy, Immunology, and Bone Marrow Transplantation, University of California San Francisco, San Francisco, California, USA.
J Clin Pharmacol ; 62(7): 873-882, 2022 07.
Article in En | MEDLINE | ID: mdl-35048362
Melphalan is an alkylating agent used as part of conditioning prior to pediatric hematopoietic cell transplantation (HCT). We performed a single-center, prospective pharmacokinetic study of 37 pediatric patients undergoing HCT from March 2015 to 2019. The primary objective was to develop and validate a population pharmacokinetic model for melphalan in a diverse group of pediatric HCT recipients. Nonlinear mixed-effects modeling was implemented to describe plasma concentration-time data of melphalan. A 2-compartment, proportional error model with weight on clearance best fit the data. Final parameter estimates were clearance, 19.1 L/h/25 kg; volume of the central compartment, 8.5 L/25 kg; volume of the peripheral compartment, 5.8 L/25 kg; and intercompartmental clearance 12.4 L/h/25 kg. Residual unexplained variability was low, at 12.5%. Results suggest the empiric weight-based dosing (mg/kg) used in children <12 kg or 2 years of age may result in subtherapeutic exposure. Model-based dosing of melphalan in pediatric HCT may help inform individualized dosing strategies to improve clinical outcomes and limit drug-related adverse events in pediatric HCT recipients.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Hematopoietic Stem Cell Transplantation / Melphalan Type of study: Observational_studies Limits: Child / Humans Language: En Journal: J Clin Pharmacol Year: 2022 Document type: Article Affiliation country: Estados Unidos Country of publication: Reino Unido

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Hematopoietic Stem Cell Transplantation / Melphalan Type of study: Observational_studies Limits: Child / Humans Language: En Journal: J Clin Pharmacol Year: 2022 Document type: Article Affiliation country: Estados Unidos Country of publication: Reino Unido