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Impact of pharmacogenetics on variability in exposure to oral vinorelbine among pediatric patients: a model-based population pharmacokinetic analysis.
Hamimed, Mourad; Leblond, Pierre; Dumont, Aurélie; Gattacceca, Florence; Tresch-Bruneel, Emmanuelle; Probst, Alicia; Chastagner, Pascal; Pagnier, Anne; De Carli, Emilie; Entz-Werlé, Natacha; Grill, Jacques; Aerts, Isabelle; Frappaz, Didier; Bertozzi-Salamon, Anne-Isabelle; Solas, Caroline; André, Nicolas; Ciccolini, Joseph.
Afiliación
  • Hamimed M; SMARTc Unit, Cancer Research Center of Marseille, Inserm U1068-CNRS UMR 7258, Aix-Marseille University U105, 27 Boulevard Jean Moulin, 13385, Marseille, France. mourad.hamimed@univ-amu.fr.
  • Leblond P; Inria-Inserm COMPO Team, Centre Inria Sophia Antipolis - Méditerranée, Inserm U1068-CNRS UMR 7258, Aix-Marseille University U105, Marseille, France. mourad.hamimed@univ-amu.fr.
  • Dumont A; Institute of Pediatric Hematology and Oncology IHOPe, Léon Bérard Cancer Center, Lyon, France.
  • Gattacceca F; Department of Pediatric Oncology, Oscar Lambret Cancer Center, Lille, France.
  • Tresch-Bruneel E; Unité d'Oncologie Moléculaire Humaine, Oscar Lambret Cancer Center, Lille, France.
  • Probst A; SMARTc Unit, Cancer Research Center of Marseille, Inserm U1068-CNRS UMR 7258, Aix-Marseille University U105, 27 Boulevard Jean Moulin, 13385, Marseille, France.
  • Chastagner P; Inria-Inserm COMPO Team, Centre Inria Sophia Antipolis - Méditerranée, Inserm U1068-CNRS UMR 7258, Aix-Marseille University U105, Marseille, France.
  • Pagnier A; Department of Biostatistics, Oscar Lambret Cancer Center, Lille, France.
  • De Carli E; Département de la Recherche Clinique et Innovation, Oscar Lambret Cancer Center, Lille, France.
  • Entz-Werlé N; Service d'Hémato-Oncologie Pédiatrique, Nancy University Hospital, Nancy, France.
  • Grill J; Service d'Hémato-Oncologie Pédiatrique, Grenoble University Hospital, Grenoble, France.
  • Aerts I; Service d'Hémato-Oncologie Pédiatrique, Angers University Hospital, Angers, France.
  • Frappaz D; Pédiatrie Onco-Hématologie Université de Strasbourg, CHRU Hautepierre, UMR CNRS 7021, Strasbourg, France.
  • Bertozzi-Salamon AI; Département de Cancérologie de l'Enfant et de l'Adolescent et UMR CNRS 8203 Université Paris Saclay, Gustave Roussy, Villejuif, France.
  • Solas C; SIREDO Centre (Care, Innovation and Research in Paediatric, Adolescent and Young Adult Oncology), Institut Curie-Oncology Center, Paris, France.
  • André N; Institute of Pediatric Hematology and Oncology IHOPe, Léon Bérard Cancer Center, Lyon, France.
  • Ciccolini J; Service d'Hémato-Oncologie Pédiatrique, Toulouse University Hospital, Toulouse, France.
Cancer Chemother Pharmacol ; 90(1): 29-44, 2022 07.
Article en En | MEDLINE | ID: mdl-35751658
ABSTRACT

PURPOSE:

Better understanding of pharmacokinetics of oral vinorelbine (VNR) in children would help predicting drug exposure and, beyond, clinical outcome. Here, we have characterized the population pharmacokinetics of oral VNR and studied the factors likely to explain the variability observed in VNR exposure among young patients. DESIGN/

METHODS:

We collected blood samples from 36 patients (mean age 11.6 years) of the OVIMA multicentric phase II study in children with recurrent/progressive low-grade glioma. Patients received 60 mg/m2 of oral VNR on days 1, 8, and 15 during the first 28-day treatment cycle and 80 mg/m2, unless contraindicated, from cycle 2-12. Population pharmacokinetic analysis was performed using nonlinear mixed-effects modeling within the Monolix® software. Fifty SNPs of pharmacokinetic-related genes were genotyped. The influence of demographic, biological, and pharmacogenetic covariates on pharmacokinetic parameters was investigated using a stepwise multivariate procedure.

RESULTS:

A three-compartment model, with a delayed double zero-order absorption and a first-order elimination, best described VNR pharmacokinetics in children. Typical population estimates for the apparent central volume of distribution (Vc/F) and elimination rate constant were 803 L and 0.60 h-1, respectively. Following covariate analysis, BSA, leukocytes count, and drug transport ABCB1-rs2032582 SNP showed a dramatic impact on Vc/F. Conversely, age and sex had no significant effect on VNR pharmacokinetics.

CONCLUSION:

Beyond canonical BSA and leukocytes, ABCB1-rs2032582 polymorphism showed a meaningful impact on VNR systemic exposure. Simulations showed that the identified covariates could have an impact on both efficacy and toxicity outcomes. Thus, a personalized dosing strategy, using those covariates, could help to optimize the efficacy/toxicity balance of VNR in children.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Farmacogenética / Modelos Biológicos Tipo de estudio: Clinical_trials / Prognostic_studies Límite: Child / Humans Idioma: En Revista: Cancer Chemother Pharmacol Año: 2022 Tipo del documento: Article País de afiliación: Francia

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Farmacogenética / Modelos Biológicos Tipo de estudio: Clinical_trials / Prognostic_studies Límite: Child / Humans Idioma: En Revista: Cancer Chemother Pharmacol Año: 2022 Tipo del documento: Article País de afiliación: Francia