Abstract
The systemic exposure to the anticancer agent irinotecan (CPT-11) and its active metabolite SN-38 were 79 and 92% reduced, respectively, relative to literature data, by concomitant phenytoin therapy. This finding suggests that increased doses of CPT-11 should be given to patients treated simultaneously with these drugs, to achieve adequate levels of SN-38.
MeSH terms
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Adult
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Anticonvulsants / pharmacology
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Antineoplastic Agents, Phytogenic / pharmacokinetics*
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Antineoplastic Agents, Phytogenic / therapeutic use*
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Brain Neoplasms / drug therapy*
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Brain Neoplasms / metabolism
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Camptothecin / analogs & derivatives
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Camptothecin / pharmacokinetics*
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Camptothecin / therapeutic use*
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Drug Interactions
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Glioma / drug therapy*
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Glioma / metabolism
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Humans
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Irinotecan
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Phenytoin / pharmacology*
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Topoisomerase I Inhibitors
Substances
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Anticonvulsants
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Antineoplastic Agents, Phytogenic
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Topoisomerase I Inhibitors
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Phenytoin
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Irinotecan
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Camptothecin