Abstract
Forty-two patients with progressive solid tumors and brain tumors were entered in this Phase I study of the glutamine antagonist acivicin given intravenously over thirty minutes daily for five days. The major toxicities encountered were myelosuppression and central nervous system toxicity (nightmares and somnolence). The maximum tolerated dosage on this schedule was 26 mg/M2 daily for five days. Six patients including three patients with brain tumor had stable disease.
Publication types
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Clinical Trial
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Clinical Trial, Phase I
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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Adolescent
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Antimetabolites, Antineoplastic / adverse effects*
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Antimetabolites, Antineoplastic / therapeutic use
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Child
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Child, Preschool
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Drug Resistance, Neoplasm
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Enzyme Inhibitors / adverse effects*
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Enzyme Inhibitors / therapeutic use
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Humans
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Injections, Intravenous
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Isoxazoles / adverse effects*
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Isoxazoles / therapeutic use
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Neoplasms / drug therapy*
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Tumor Cells, Cultured / drug effects
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gamma-Glutamyltransferase / antagonists & inhibitors
Substances
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Antimetabolites, Antineoplastic
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Enzyme Inhibitors
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Isoxazoles
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gamma-Glutamyltransferase
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acivicin