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Erschienen in: Cancer Chemotherapy and Pharmacology 5/2014

01.05.2014 | Original Article

Rate and extent of oxaliplatin absorption after hyperthermic intraperitoneal administration in peritoneal carcinomatosis patients

verfasst von: Carlos Pérez-Ruixo, José E. Peris, Vanesa Escudero-Ortiz, Pedro Bretcha-Boix, José Farré-Alegre, Juan José Pérez-Ruixo, Belén Valenzuela

Erschienen in: Cancer Chemotherapy and Pharmacology | Ausgabe 5/2014

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Abstract

Purpose

To determine the rate and extent of hyperthermic intraperitoneal oxaliplatin (HIO) absorption in peritoneal carcinomatosis patients treated with cytoreductive surgery (CRS) and the effect of the isotonic carrier solution on HIO absorption parameters.

Methods

Full pharmacokinetic profiles collected in peritoneum and plasma from 57 subjects treated with CRS followed by 30 min of HIO were pooled with sparse plasma concentrations collected from 50 patients with solid tumors treated with intravenous oxaliplatin. Pharmacokinetic data were jointly analyzed with nonlinear mixed-effect model (NONMEM VII software). The effect of carrier solution (icodextrin 4 % vs. dextrose 5 %) and selected patient covariates on oxaliplatin pharmacokinetics was investigated. Model evaluation was performed using predictive checks and nonparametric bootstrap.

Results

An open linear two-compartment disposition model with linear absorption from peritoneum to plasma was used to characterize the oxaliplatin pharmacokinetics in peritoneum and plasma. No patient-related covariates were associated with oxaliplatin pharmacokinetics. The volume of distribution in the peritoneum (V a) exponentially decreased due to the carrier solute absorption. The reduction in V a was 1.76-fold faster when HIO was administered in dextrose 5 %, relative to icodextrin 4 %. For HIO durations of 30 min, the rate of oxaliplatin absorption ranges from 0.84 to 0.96 h−1 for icodextrin 4 % and from 0.86 to 1.09 h−1 for dextrose 5 %. The extent of HIO absorption was 38 %, regardless of the carrier solution.

Conclusions

Hyperthermic intraperitoneal oxaliplatin absorption is fast and incomplete. The small difference in oxaliplatin exposure between both carrier solutions evaluated is not clinically relevant for HIO durations of 30 min.
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Metadaten
Titel
Rate and extent of oxaliplatin absorption after hyperthermic intraperitoneal administration in peritoneal carcinomatosis patients
verfasst von
Carlos Pérez-Ruixo
José E. Peris
Vanesa Escudero-Ortiz
Pedro Bretcha-Boix
José Farré-Alegre
Juan José Pérez-Ruixo
Belén Valenzuela
Publikationsdatum
01.05.2014
Verlag
Springer Berlin Heidelberg
Erschienen in
Cancer Chemotherapy and Pharmacology / Ausgabe 5/2014
Print ISSN: 0344-5704
Elektronische ISSN: 1432-0843
DOI
https://doi.org/10.1007/s00280-014-2436-6

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