TY - JOUR T1 - Probenecid Alters Topotecan Systemic and Renal Disposition by Inhibiting Renal Tubular Secretion JF - Journal of Pharmacology and Experimental Therapeutics JO - J Pharmacol Exp Ther SP - 89 LP - 94 VL - 284 IS - 1 AU - William C. Zamboni AU - Peter J. Houghton AU - Randall K. Johnson AU - Jeff L. Hulstein AU - William R. Crom AU - Pam J. Cheshire AU - Suzan K. Hanna AU - Lois B. Richmond AU - Xiaolong Luo AU - Clinton F. Stewart Y1 - 1998/01/01 UR - http://jpet.aspetjournals.org/content/284/1/89.abstract N2 - Topotecan is primarily eliminated by the kidneys, with 60 to 70% of the dose recovered as topotecan total in the urine. To elucidate the mechanisms of topotecan renal clearance, we evaluated the effect of probenecid on topotecan renal and systemic disposition in mice. Topotecan lactone or hydroxy acid (1.25 mg/kg i.v.) was administered alone or in combination with probenecid (600 or 1200 mg/kg) given by oral gavage 30 min before and 3 hr after topotecan. Serial blood samples (three mice per time point) and urine samples (five mice per treatment arm) were collected during a 6-hr period. Compared with topotecan alone, coadministration of topotecan lactone or hydroxy acid with probenecid (600 mg/kg) decreased topotecan lactone, total, and hydroxy acid systemic clearance, and total renal clearance. The predominant effect of probenecid was to increase hydroxy acid area under the plasma concentration time curve after administration of topotecan lactone (238.8 vs. 109.9 ng·hr/ml alone, P < .05), or hydroxy acid (1297.2 vs. 355.0 ng·hr/ml alone, P < .05). By inhibiting renal tubular secretion, probenecid decreased renal and systemic clearance which led to an increase in topotecan systemic exposure. These data suggest that probenecid primarily inhibited secretion of the anionic hydroxy acid form, and by direct or indirect mechanisms increased topotecan lactone systemic exposure. Topotecan elimination through renal tubular secretion may have clinical relevance for the use of topotecan in patients with altered renal function. The American Society for Pharmacology and Experimental Therapeutics ER -