Aprepitant when added to a standard antiemetic regimen consisting of ondansetron and dexamethasone does not affect vinorelbine pharmacokinetics in cancer patients |
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Authors: | Walter J. Loos Ronald de Wit Steven J. Freedman Kristien Van Dyck Jay J. Gambale Susie Li Gail M. Murphy Connie van Noort Peter de Bruijn Jaap Verweij |
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Affiliation: | (1) Department of Medical Oncology, Erasmus MC—Daniel den Hoed Cancer Center Rotterdam, P.O. Box 5201, 3008 AE Rotterdam, The Netherlands;(2) Merck Research Laboratories, West Point, PA 19486, USA |
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Abstract: | Purpose Aprepitant, a selective neurokinin-1 (NK-1) receptor antagonist approved for the treatment and prevention of emesis caused
by moderately and highly emetogenic chemotherapy, is an inhibitor, inducer, and substrate of the cytochrome P450 3194 pathway.
The CYP3A4 pathway is the major pathway of the metabolism of vinorelbine, a vinca alkaloid frequently used in combination
with cisplatin. Therefore, we studied the potential interaction of the aprepitant 3-day antiemetic regimen on the pharmacokinetics
of vinorelbine.
Patients and methods Fourteen patients with metastatic solid tumors were included in this open-label, balanced, 2-period crossover study. In treatment
arm A, vinorelbine (25 mg/m2 weekly) was administered alone, while in treatment arm B the same dose of vinorelbine was administered following the administration
of the aprepitant antiemetic regimen on day 1 and alone on day 8. The antiemetic regimen of aprepitant was comprised of the
following; on day 1: 125 mg aprepitant, 12 mg dexamethasone, and 32 mg ondansetron; on days 2 and 3: 80 mg aprepitant and
8 mg dexamethasone and on day 4: 8 mg dexamethasone. Blood samples for vinorelbine pharmacokinetic analysis were collected
over 96 h.
Results Two patients discontinued the study due to adverse events that were judged not to be drug-related. Complete pharmacokinetic
data of vinorelbine administered alone and with the aprepitant antiemetic regimen were obtained in 12 patients. The mean plasma
concentration profile of vinorelbine administered with aprepitant was identical to that following vinorelbine administered
alone, with geometric mean vinorelbine plasma AUC ratios of treatment B day 1/treatment A day 1 and of treatment B day 8/treatment
A day of 1.01 (0.93, 1.10) and 1.00 (0.92, 1.08), respectively.
Conclusion As the aprepitant antiemetic regimen has no detectable inhibitory or inductive effect on the pharmacokinetics of vinorelbine,
aprepitant when added to a standard antiemetic regimen consisting of ondansetron and dexamethasone can be safely combined
with vinorelbine at clinically recommended doses. |
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Keywords: | Aprepitant Vinorelbine CYP3A4 Interaction Pharmacokinetics |
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