Relationship Between Sunitinib Pharmacokinetics and Administration Time: Preclinical and Clinical Evidence

Jacqueline Kloth, Lisette Binkhorst, Annelieke Wit, Peter de Bruijn, P Hamberg, Mei Lam, H (Hens) Burger, I Chaves, Erik Wiemer, Bert van der Horst, Ron Mathijssen

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Background and Objective Circadian rhythms may influence the pharmacokinetics of drugs. This study aimed to elucidate whether the pharmacokinetics of the orally administered drug sunitinib are subject to circadian variation. Methods We performed studies in male FVB-mice aged 8-12 weeks, treated with single-dose sunitinib at six dosing times. Plasma and tissue samples were obtained for pharmacokinetic analysis and to monitor messenger RNA (mRNA) expression of metabolizing enzymes and drug transporters. A prospective randomized crossover study was performed in which patients took sunitinib once daily at 8 a.m., 1 p.m., and 6 p.m at three subsequent courses. Patients were blindly randomized into two groups, which determined the sequence of the sunitinib dosing time. The primary endpoint in both studies was the difference in plasma area under the concentration-time curve (AUC) of sunitinib and its active metabolite SU12662 between dosing times. Results Sunitinib and SU12662 plasma AUC in mice followed an similar to 12-h rhythm as a function of administration time (p <= 0.04). The combined AUC from time zero to 10 h (AUC(10)) was 14-27 % higher when sunitinib was administered at 4 a.m. and 4 p.m. than at 8 a.m. and 8 p.m. Twenty-four-hour rhythms were seen in the mRNA levels of drug transporters and metabolizing enzymes. In 12 patients, sunitinib trough concentrations (C (trough)) were higher when the drug was taken at 1 p.m. or 6 p.m. than when taken at 8 a.m. (C (trough-1 p.m). 66.0 ng/mL; C (trough-6 p.m.) 58.9 ng/mL; C (trough-8 a.m.) 50.7 ng/mL; p = 0.006). The AUC was not significantly different between dosing times. Conclusions Our results indicate that sunitinib pharmacokinetics follow an similar to 12-h rhythm in mice. In humans, morning dosing resulted in lower C (trough) values, probably resulting from differences in elimination. This can have implications for therapeutic drug monitoring.
Original languageUndefined/Unknown
Pages (from-to)851-858
Number of pages8
JournalClinical Pharmacokinetics
Issue number8
Publication statusPublished - 2015

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