期刊
INVESTIGATIONAL NEW DRUGS
卷 22, 期 2, 页码 139-150出版社
KLUWER ACADEMIC PUBL
DOI: 10.1023/B:DRUG.0000011790.31292.ef
关键词
clinical trials; signal transduction inhibitor; chemotherapy; pharmacokinetics
Purpose: 4'-N-Benzoyl-staurosporine (PKC412) is an orally available staurosporine derivative that inhibits protein kinase C. The objectives of this phase I trial were to determine the maximum tolerated dose (MTD), the dose limiting toxicities (DLTs), and the pharmacokinetics of PKC412 when co-administered with 5-Fluorouracil (5-FU). Experimental design: PKC412 was given daily with a 21-day continuous i.v. infusion of 5-FU 200 mg/m(2)/day, repeated every 4 weeks. The PKC412 dose was escalated by a modified continual reassessment method. The steady-state plasma pharmacokinetics of 5-FU, PKC412, and two of its circulating metabolites were determined during the first cycle of therapy. Results: A total of 33 patients were treated with 70 cycles (median: 2, range: 1-4) of PKC412 at doses ranging from 25 to 225 mg/day. No significant toxicities were encountered with doses up to 150 mg/day. Among nine patients treated with 225 mg/day of PKC412, one experienced grade 3 fatigue and nausea, another developed grade 3 hyperglycemia, and three had grade 2 emesis and stomatitis, leading to early treatment discontinuation. Minor responses consisting of a 40-45% tumor reduction were observed in two patients, one with gall bladder carcinoma and one with breast cancer. Mean values of steady-state pharmacokinetic variables for both PKC412 and 5-FU were comparable to single agent studies. Conclusions: The recommended phase II dose of PKC412 is 150 mg/day when combined with a continuous infusion of 200 mg/m(2)/day 5-FU. The dose limiting toxicity was grade 2 emesis and stomatitis and the regimen showed indications of activity. There was no evidence of a pharmacokinetic interaction between the two drugs.
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