Literature DB >> 9654117

Renal toxicity of the anticancer drug fostriecin.

R S de Jong1, E G de Vries, S Meijer, P E de Jong, N H Mulder.   

Abstract

PURPOSE: Fostriecin is an inhibitor of topoisomerase II catalytic activity. In a phase I trial we observed renal toxicity, documented as a rise in serum creatinine, which was reversible and non-dose-limiting. The purpose of this study was a detailed analysis of this toxicity.
METHODS: A total of 20 patients received fostriecin as a 1-h i.v. infusion daily x 5 at doses ranging from 2 to 20 mg/m2 per day. Serum creatinine determination and urinalysis were performed daily during drug administration. Renal hemodynamics were measured by means of clearance studies using 125I-iothalamate and (131)I-hippuran in eight patients at doses of > or =4 mg/m2 per day at baseline, on day 3 or 4 during the first course, and 3 weeks after the second course.
RESULTS: The rise in serum creatinine was maximal after one to two doses despite continued administration. This increase showed no correlation with the dose level at fostriecin doses of > or =4 mg/m2 per day. Urinary beta2-microglobulin concentrations increased 150-fold (median), which is compatible with impaired tubular reabsorption. The median change in the glomerular filtration rate (GFR) was -36% (range -28% to -44%), that in effective renal plasma flow (ERPF) was -23% (range -11% to -36%), and the filtration fraction (FF) decreased in all patients during the first course of treatment. The values measured 3 weeks after the second course, however, did not differ from baseline.
CONCLUSIONS: Fostriecin induces reversible renal hemodynamic changes compatible with renal tubular damage.

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Year:  1998        PMID: 9654117     DOI: 10.1007/s002800050800

Source DB:  PubMed          Journal:  Cancer Chemother Pharmacol        ISSN: 0344-5704            Impact factor:   3.333


  4 in total

1.  Anticancer activity and protein phosphatase 1 and 2A inhibition of a new generation of cantharidin analogues.

Authors:  Jennette A Sakoff; Stephen P Ackland; Monique L Baldwin; Mirella A Keane; Adam McCluskey
Journal:  Invest New Drugs       Date:  2002-02       Impact factor: 3.850

2.  Phase I and pharmacokinetic study of fostriecin given as an intravenous bolus daily for five consecutive days.

Authors:  Lyly H Lê; Charles Erlichman; Linda Pillon; Jake J Thiessen; Andrew Day; Nancy Wainman; Elizabeth A Eisenhauer; Malcolm J Moore
Journal:  Invest New Drugs       Date:  2004-04       Impact factor: 3.850

3.  Protein phosphatase 2A enhances activation of human immunodeficiency virus type 1 by phorbol myristate acetate.

Authors:  Neil E Faulkner; Brian R Lane; Paul J Bock; David M Markovitz
Journal:  J Virol       Date:  2003-02       Impact factor: 5.103

4.  Phase I and pharmacokinetic study of the topoisomerase II catalytic inhibitor fostriecin.

Authors:  R S de Jong; N H Mulder; D R Uges; D T Sleijfer; F J Höppener; H J Groen; P H Willemse; W T van der Graaf; E G de Vries
Journal:  Br J Cancer       Date:  1999-02       Impact factor: 7.640

  4 in total

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