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Population pharmacokinetic model of irinotecan and its four main metabolites in patients treated with FOLFIRI or FOLFIRINOX regimen.
Deyme, Laure; Barbolosi, Dominique; Mbatchi, Litaty Céphanoée; Tubiana-Mathieu, Nicole; Ychou, Marc; Evrard, Alexandre; Gattacceca, Florence.
Afiliación
  • Deyme L; SMARTc, Centre de Recherche en Cancérologie de Marseille (CRCM), Faculté de Pharmacie, INSERM U1068, CNRS UMR 7258, Aix-Marseille Université and Institut Paoli-Calmettes, Marseille, France. laure.deyme@gmail.com.
  • Barbolosi D; SMARTc, Centre de Recherche en Cancérologie de Marseille (CRCM), Faculté de Pharmacie, INSERM U1068, CNRS UMR 7258, Aix-Marseille Université and Institut Paoli-Calmettes, Marseille, France.
  • Mbatchi LC; Laboratoire de Biochimie et Biologie Moléculaire, CHU Nîmes-Carémeau, Nîmes, France.
  • Tubiana-Mathieu N; IRCM, Inserm U1194, Université de Montpellier, Montpellier, France.
  • Ychou M; Centre Hospitalier Universitaire de Limoges, Limoges, France.
  • Evrard A; Institut Régional du Cancer de Montpellier (ICM)-Val d'Aurelle, Montpellier, France.
  • Gattacceca F; Laboratoire de Biochimie et Biologie Moléculaire, CHU Nîmes-Carémeau, Nîmes, France.
Cancer Chemother Pharmacol ; 88(2): 247-258, 2021 08.
Article en En | MEDLINE | ID: mdl-33912999
ABSTRACT

PURPOSE:

The aim of the present study was to characterize the pharmacokinetics of irinotecan and its four main metabolites (SN-38, SN-38G, APC and NPC) in metastatic colorectal cancer patients treated with FOLFIRI and FOLFIRINOX regimens and to quantify and explain the inter-individual pharmacokinetic variability in this context.

METHODS:

A multicenter study including 109 metastatic colorectal cancer patients treated with FOLFIRI or FOLFIRINOX regimen, associated or not with a monoclonal antibody, was conducted. Concentrations of irinotecan and its four main metabolites were measured in 506 blood samples during the first cycle of treatment. Collected data were analyzed using the population approach. First, fixed and random effects models were selected using statistical and graphical methods; second, the impact of covariates on pharmacokinetic parameters was evaluated to explain the inter-individual variability in pharmacokinetic parameters.

RESULTS:

A seven-compartment model best described the pharmacokinetics of irinotecan and its four main metabolites. First-order rates were assigned to distribution, elimination, and metabolism processes, except for the transformation of irinotecan to NPC which was nonlinear. Addition of a direct conversion of NPC into SN-38 significantly improved the model. Co-administration of oxaliplatin significantly modified the distribution of SN-38.

CONCLUSION:

To our knowledge, the present model is the first to allow a simultaneous description of irinotecan pharmacokinetics and of its four main metabolites. Moreover, a direct conversion of NPC into SN-38 had never been described before in a population pharmacokinetic model of irinotecan. The model will be useful to develop pharmacokinetic-pharmacodynamic models relating SN-38 concentrations to efficacy and digestive toxicities. CLINICAL TRIALS REGISTRATION NUMBER ClinicalTrials.gov identifier NCT00559676.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Camptotecina / Protocolos de Quimioterapia Combinada Antineoplásica / Inhibidores de Topoisomerasa I / Irinotecán Tipo de estudio: Clinical_trials / Prognostic_studies Límite: Female / Humans / Male Idioma: En Revista: Cancer Chemother Pharmacol Año: 2021 Tipo del documento: Article País de afiliación: Francia

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Camptotecina / Protocolos de Quimioterapia Combinada Antineoplásica / Inhibidores de Topoisomerasa I / Irinotecán Tipo de estudio: Clinical_trials / Prognostic_studies Límite: Female / Humans / Male Idioma: En Revista: Cancer Chemother Pharmacol Año: 2021 Tipo del documento: Article País de afiliación: Francia
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