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Pharmacokinetics and safety of cetuximab in a patient with renal dysfunction
L L Krens1, J M Baas, M C Verboom
1Department of Clinical Pharmacy and Toxicology, Leiden University Medical Center, PO Box 9600 NL, 2300 RC, Leiden, The Netherlands, l.l.krens@lumc.nl.
Introduction:
In the literature, data on the effect of renal impairment on the pharmacokinetics of anticancer drugs are scarce. Here, we report a 68-year-old metastatic osteosarcoma patient with impaired renal function due to prior chemotherapy, who was treated on compassionate use basis with 400 mg/m(2) cetuximab.
Material And Methods:
Pharmacokinetic parameters after the first dose, including dose-normalised AUC from time zero to day 7, clearance, elimination half-life (t(1/2)), were estimated using trapezoidal non-compartmental methods and compared to pharmacokinetic data from a study population with normal kidney function.
Results:
The results showed that the pharmacokinetics of cetuximab in this patient with renal failure was similar to that with adequate renal function.
Conclusion:
This study suggests that cetuximab can be safely used in cancer patients with renal impairment without dose adjustment.
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