Abstract

Background: The human cytochrome P450 enzyme CYP3A4 is involved in the metabolism of many anticancer drugs. Since these drugs are usually administered in a polychemotherapy regimen, the objective of this study was to examine their inhibitory potency on CYP3A4 with regard to possible mutual drug interactions. Method: CYP3A4 activities in human liver microsomes from 2 donors were determined using the oxidation of the dihydropyridine denitronifedipine, a specific CYP3A4 substrate, at a concentration of 50 mM (= KM). Formation of the pyridine metabolite was measured using HPLC. Inhibitor concentrations used were 0.5, 5 and 50 mg/ml, except for cyclophosphamide and ifosfamide (0.5, 2.5 and 5 mg/ml) and for paclitaxel (0.05, 0.15, 0.5, 1.5 and 5 mg/ml). Results: The following substances showed an inhibitory effect on CYP3A4 (IC50 values for the 2 microsome samples are parenthesized): cyclophosphamide (12.3/9.2 mmol/l), mafosfamide generated 4-OH-cyclophosphamide (152/163 mmol/l), ifosfamide (3.6/2.5 mmol/l), vinblastine sulfate (20/44 mmol/l), vincristine sulfate (67/176 mmol/l), daunorubicin hydrochloride (206/200 mmol/l), doxorubicin hydrochloride (160/215 mmol/l), teniposide (64/84 mmol/l) and docetaxel (6.4/12.7 mmol/l). No inhibitory effect on CYP3A4 was observed with epirubicin, etoposide, paclitaxel, cytarabine, 5-FU, 6-mercaptopurine, methotrexate, cisplatin, carboplatin, bleomycin, busulfan, chlorambucil and mitomycin. Conclusion: Comparing IC50 values with plasma concentrations present during antineoplastic therapy, the agents cyclophosphamide, ifosfamide, vinblastine, teniposide and docetaxel could possibly cause clinical drug interactions by inhibition of CYP3A4. Some recently described clinical interactions with antineoplastic agents may be explained by these results.

Author Details

Authors

• M. Baumhäkel¹
• D. Kasel¹
• R.A. Rao-Schymanski¹
• R. Böcker²
• K.T. Beckurts³
• M. Zaigler¹
• D. Barthold¹
• U. Fuhr¹

Departments

• ¹ Clinical Pharmacology, Institute for Pharmacology, University of Köln,
• ² Department of Experimental and Clinical Pharmacology and Toxicology, University of Erlangen, and
• ³ Department of Visceral and Vascular Surgery, University of Köln, Germany

Address

Prof. Dr. U. Fuhr; Institut für Pharmakologie, Klinische Pharmakologie, Universität zu Köln,
Gleueler Straße 24, D-50931 Köln, Germany
Email: [email protected]

Citation