The effect of anastrozole on the single‐dose pharmacokinetics and anticoagulant activity of warfarin in healthy volunteers
Open Access
- 1 May 2001
- journal article
- clinical trial
- Published by Wiley in British Journal of Clinical Pharmacology
- Vol. 51 (5), 429-435
- https://doi.org/10.1046/j.1365-2125.2001.01358.x
Abstract
Aims The aims of this study were to determine the effects of the nonsteroidal, selective aromatase inhibitor, anastrozole, at steady‐state concentrations, on the pharmacokinetics and pharmacodynamics of warfarin, and to assess whether or not anastrozole alone has any anticoagulant activity. Methods This was a randomized, double‐blind, placebo‐controlled, two‐way crossover trial conducted at a single centre. The study comprised two treatment periods of 11 days, separated by a 3 week washout. Healthy male volunteers (n = 16, median age 28.5 years) were randomized to receive either anastrozole (7 mg loading dose on day 1, followed by 1 mg daily on days 2–11) in the first treatment period and placebo in the second treatment period, or vice versa. In addition to their randomized treatment, all volunteers received a single dose of 25 mg warfarin on day 3 of each treatment period. Blood samples for pharmacokinetic and pharmacodynamic assessment were taken at frequent intervals during each treatment period. The safety of volunteers was monitored throughout the study. Results Administration of anastrozole resulted in no clinically significant changes in the pharmacokinetics of either R‐ or S‐warfarin compared with placebo for AUC (ng ml−1 h) (glsmean, R‐warfarin; anastrozole 93619.9, placebo 91127.91, 95%CI 0.988–1.068; S‐warfarin; anastrozole 57129.21, placebo 55676.34, 95%CI 0.979–1.076), CL/F (ml min−1) (glsmean, R‐warfarin; anastrozole 2.23, placebo 2.29, 95%CI 0.937–1.012; S‐warfarin; anastrozole 3.65, placebo 3.74, 95%CI 0.929–1.021) and t1/2 (h) (lsmean, R‐warfarin; anastrozole 55.40, placebo 55.15, 95%CI−2.083–2.592; S‐warfarin; anastrozole 39.38, placebo 40.98, 95%CI−6.189–2.996). In addition, anastrozole had no clinically significant effect on the pharmacodynamic effects of warfarin, as assessed 240 h after warfarin dosing by measurement of prothrombin time (s) (glsmean, anastrozole 11.56, placebo 11.31, 95%CI 0.987–1.059), thrombin time (s) (glsmean, anastrozole 19.06, placebo 18.75, 95%CI 0.980–1.054) activated partial thromboplastin time (s) (glsmean, anastrozole 29.94, placebo 29.74, 95%CI 0.968–1.047) and factor VII (%) (glsmean, anastrozole 97.81, placebo 107.26, 95%CI 0.821–1.012). Anastrozole alone had no effect on these indicators of the clotting process. Conclusions Overall, there was no evidence to suggest that anastrozole has any clinically relevant effects on the pharmacokinetics of warfarin. Anastrozole had no effect on clotting mechanisms or on the pharmacodynamic activity of warfarin, as assessed by prothrombin time, thrombin time, activated partial thromboplastin time, and factor VII.Keywords
This publication has 11 references indexed in Scilit:
- Update: Clinically Significant Cytochrome P‐450 Drug InteractionsPharmacotherapy: The Journal of Human Pharmacology and Drug Therapy, 1998
- Validated assay for the quantification of anastrozole in human plasma by capillary gas chromatography-63Ni electron capture detectionJournal of Chromatography B: Biomedical Sciences and Applications, 1997
- Inhibition of human drug metabolizing cytochromes P450 by anastrozole, a potent and selective inhibitor of aromatase.1997
- Clinically Important Drug Interactions with AnticoagulantsClinical Pharmacokinetics, 1996
- Interactions of Warfarin with Drugs and FoodAnnals of Internal Medicine, 1994
- Arimidex : A potent and selective fourth-generation aromatase inhibitorBreast Cancer Research and Treatment, 1994
- Drug interactions with warfarinThe Medical Journal of Australia, 1992
- Life threatening interaction between tamoxifen and warfarin.BMJ, 1989
- Life threatening interaction between tamoxifen and warfarin.BMJ, 1987
- Aminoglutethimide and warfarinCancer Chemotherapy and Pharmacology, 1984