Abstract
Carboplatin is an alternative for cisplatin in the treatment of urothelial cancers. A pharmacologically guided phase I study of carboplatin in combination with methotrexate (30 mg/m2) and vinblastine (4 mg/m2) was conducted in ten patients by increment of the area under the plasma concentration versus time curve (AUC) for ultrafilterable carboplatin using the Calvert formula. The maximal tolerated AUC was 5 mg ml-1 min, with neutropenia being the dose-limiting toxicity. There was a significant linear correlation between the percentage of decrease in neutrophil count and the carboplatin AUC. Determination of the glomerular filtration rate by the isotopic method allowed us to adapt the dose of carboplatin given to patients suffering from urothelial cancer, who frequently have impaired renal function. The recommended AUC for phase II study is 4 mg ml-1 min.
Publication types
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Clinical Trial
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Clinical Trial, Phase I
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Research Support, Non-U.S. Gov't
MeSH terms
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Antineoplastic Combined Chemotherapy Protocols / adverse effects
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Antineoplastic Combined Chemotherapy Protocols / pharmacokinetics
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Antineoplastic Combined Chemotherapy Protocols / therapeutic use*
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Carboplatin / administration & dosage
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Carboplatin / adverse effects
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Carboplatin / pharmacokinetics
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Carcinoma, Transitional Cell / drug therapy*
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Cell Count / drug effects
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Edetic Acid / metabolism
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Female
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Glomerular Filtration Rate / drug effects
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Humans
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Infusions, Intravenous
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Kidney Neoplasms / drug therapy
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Linear Models
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Male
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Methotrexate / administration & dosage
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Methotrexate / adverse effects
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Methotrexate / pharmacokinetics
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Middle Aged
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Neutropenia / chemically induced
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Neutrophils / drug effects
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Thrombocytopenia / chemically induced
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Ultrafiltration
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Ureteral Neoplasms / drug therapy
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Urinary Bladder Neoplasms / drug therapy
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Urologic Neoplasms / drug therapy*
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Vinblastine / administration & dosage
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Vinblastine / adverse effects
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Vinblastine / pharmacokinetics
Substances
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Vinblastine
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Edetic Acid
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Carboplatin
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Methotrexate