Pediatric phase I trial and pharmacokinetic study of tiazofurin (NSC 286193)

Tiazofurin (2-beta-D-ribofuranosylthiazole-4-carboxamide), a new nucleoside antimetabolite, was evaluated in a phase I trial involving children with refractory cancers. The drug was administered i.v. as a 10-min infusion daily for 5 consecutive days repeated at 3-week intervals. The dose ranged from...

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Published inCancer research (Chicago, Ill.) Vol. 45; no. 10; pp. 5169 - 5172
Main Authors Balis, F M, Lange, B J, Packer, R J, Holcenberg, J S, Ettinger, L J, Sallan, S E, Heideman, R L, Zimm, S, Smithson, W A, Cogliano-Shutta, N A
Format Journal Article
LanguageEnglish
Published United States 01.10.1985
Subjects
Adolescent
Adult
Antineoplastic Agents - therapeutic use
Child
Child, Preschool
Drug Evaluation
Humans
Kidney - drug effects
Kinetics
Neoplasms - drug therapy
Ribavirin - adverse effects
Ribavirin - analogs & derivatives
Ribavirin - metabolism
Ribavirin - therapeutic use
Ribonucleosides - therapeutic use
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Summary:Tiazofurin (2-beta-D-ribofuranosylthiazole-4-carboxamide), a new nucleoside antimetabolite, was evaluated in a phase I trial involving children with refractory cancers. The drug was administered i.v. as a 10-min infusion daily for 5 consecutive days repeated at 3-week intervals. The dose ranged from 550 to 3300 mg/sq m/day. Seventeen patients received 23 courses and were evaluable for toxicity. The maximally tolerated dose was 2200 mg/sq m/day. The major dose-limiting toxicities were nonhematological. Neurotoxicity, including headache, drowsiness, and irritability, was common and was the principal dose-limiting toxicity at the higher doses. Severe myalgias were also dose limiting in one patient. Other side effects were mild, reversible elevations in serum transaminases; nausea, vomiting, and diarrhea; mild hypertension; dysphagia; and exfoliative dermatitis of the hands and feet. Myelotoxicity was not significant. The pharmacokinetics of tiazofurin was studied in 16 patients. Plasma disappearance was triphasic with half-lives of 9.7 min, 1.6 h, and 5.5 h. Clearance was dose related, ranging from 120 ml/min/sq m at 550 mg/sq m/day to 70 ml/min/sq m at 3300 mg/sq m/day. The primary route of elimination was renal with 85% of the drug recoverable in the urine as the parent compound in the 24 h following administration.
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ISSN:0008-5472
1538-7445