PT  - JOURNAL ARTICLE
AU  - T Walle
AU  - U K Walle
AU  - G N Kumar
AU  - K N Bhalla
TI  - Taxol metabolism and disposition in cancer patients.
DP  - 1995 Apr 01
TA  - Drug Metabolism and Disposition
PG  - 506--512
VI  - 23
IP  - 4
4099  - http://dmd.aspetjournals.org/content/23/4/506.short
4100  - http://dmd.aspetjournals.org/content/23/4/506.full
SO  - Drug Metab Dispos1995 Apr 01; 23
AB  - The objective of this study was to determine the metabolic fate and disposition of taxol in cancer patients. Five patients received 225 or 250 mg/m2 of taxol together with 100 microCi of [3H]taxol as a 3-hr infusion, followed by cisplatin and 5-fluorouracil. Urine, feces, and blood samples were collected for 120 hr and analyzed for total radioactivity, taxol, and metabolites by reversed-phase HPLC and tandem MS. Total urinary excretion was 14.3 +/- 1.4% (SE) of the dose, with unchanged taxol and an unknown polar metabolite as the main excretion products. Total fecal excretion was 71.1 +/- 8.2%, with 6 alpha-hydroxytaxol being the largest component by far. Unchanged taxol and four other metabolites could also be identified from fecal extracts. The plasma area under the curve for unchanged taxol was 20.5 +/- 2.3 microM.hr and that for total taxol metabolites was 14.2 +/- 4.5 microM.hr. The half-life of total metabolites (5.6 +/- 0.4 hr), however, greatly exceeded that of unchanged taxol (2.9 +/- 0.3 hr). Thus, at 5-hr posttaxol infusion, the plasma concentrations of the five metabolites together exceeded the taxol concentration by 2.4-fold. The findings from this study should be of importance as a guide to further therapeutic evaluation of this drug.