OBJECTIVE To investigate the disposition of floxuridine in patients with trophoblastic tumors.METHODS 12 patients with trophoblastic tumors were divided into FUDR and FUDR+KSM group.FUDR was administered by an 8 hour infusion.The blood samples were obtained during the infusion and up to 50 min after the infusion.The concentrations of floxuridine in serum were measured by a reverse phase high performance liquid chromatography.The pharmacokinetics of floxuridine was assessed by noncompartment and compartment model.RESULTS The disposition of floxuridine was nonlinear,consistent with a three compartment model.The metabolite fluorouracil was found after iv administration of floxuridine.CONCLUSION Floxuridine was eliminated primarily by a dose dependent process.Such characteristics may be related to unexpected stronger pharmacological effects if increasing the dose or reducing the infusion time.