Thalidomide does not alter estrogen-progesterone hormone single dose pharmacokinetics
- PMID: 10340913
- DOI: 10.1016/S0009-9236(99)70067-6
Thalidomide does not alter estrogen-progesterone hormone single dose pharmacokinetics
Abstract
Objectives: To determine the single- and multiple-dose pharmacokinetics of oral thalidomide (200 mg/day, administered for 21 days) and to assess the effects of steady-state plasma concentrations of thalidomide on the single-dose pharmacokinetics of ethinyl estradiol (INN, ethinylestradiol) and norethindrone (INN, norethisterone).
Methods: A randomized, 2-period crossover study was performed in 10 healthy premenopausal female volunteers. The pharmacokinetic profiles of plasma concentrations of thalidomide were evaluated with both noncompartmental and compartmental methods, whereas those of ethinyl estradiol and norethindrone were calculated with noncompartmental methods. The effects of steady-state plasma thalidomide concentrations on the pharmacokinetics of ethinyl estradiol and norethindrone were determined with use of an ANOVA model that included treatment sequence, subject within sequence, period, and treatment as factors.
Results: Thalidomide plasma concentrations were best predicted by a 1-compartment model with first-order absorption and elimination and an absorption time-lag. There were no significant differences between pharmacokinetic parameters for thalidomide after 1 dose and those after 18 consecutive doses. Except for a minor decrease of the elimination rate constant (k(e)) for ethinyl estradiol, coadministration of thalidomide had no significant effects on the pharmacokinetic profiles for either ethinyl estradiol or norethindrone. The change in k(e) for ethinyl estradiol during thalidomide administration was not associated with any alteration in the clearance or elimination half-life for this hormone.
Conclusions: Multiple-dose pharmacokinetics of thalidomide is similar to the single-dose profile. This study did not investigate the efficacy of the 21-day fixed ethinyl estradiol-norethindrone regimen, but the results suggest that thalidomide is unlikely to affect the pharmacokinetics of orally administered hormonal contraceptives.
Similar articles
-
Clinical pharmacokinetics of thalidomide.Clin Pharmacokinet. 2004;43(5):311-27. doi: 10.2165/00003088-200443050-00004. Clin Pharmacokinet. 2004. PMID: 15080764 Review.
-
Thalidomide does not alter the pharmacokinetics of ethinyl estradiol and norethindrone.Clin Pharmacol Ther. 1998 Dec;64(6):597-602. doi: 10.1016/S0009-9236(98)90050-9. Clin Pharmacol Ther. 1998. PMID: 9871424 Clinical Trial.
-
The effects of rifampin and rifabutin on the pharmacokinetics and pharmacodynamics of a combination oral contraceptive.Clin Pharmacol Ther. 1999 Apr;65(4):428-38. doi: 10.1016/S0009-9236(99)70138-4. Clin Pharmacol Ther. 1999. PMID: 10223781 Clinical Trial.
-
Effect of zonisamide on the pharmacokinetics and pharmacodynamics of a combination ethinyl estradiol-norethindrone oral contraceptive in healthy women.Clin Ther. 2004 Dec;26(12):2056-65. doi: 10.1016/j.clinthera.2004.11.019. Clin Ther. 2004. PMID: 15823769 Clinical Trial.
-
Pharmacokinetics of ethynyloestradiol in humans.Methods Find Exp Clin Pharmacol. 1982;4(2):133-41. Methods Find Exp Clin Pharmacol. 1982. PMID: 6750279 Review.
Cited by
-
Thalomid (Thalidomide) capsules: a review of the first 18 months of spontaneous postmarketing adverse event surveillance, including off-label prescribing.Drug Saf. 2001;24(2):87-117. doi: 10.2165/00002018-200124020-00002. Drug Saf. 2001. PMID: 11235821 Review.
-
Safety and pharmacokinetics of thalidomide in tumor-bearing dogs.J Vet Med Sci. 2023 Dec 6;85(12):1261-1268. doi: 10.1292/jvms.23-0200. Epub 2023 Oct 10. J Vet Med Sci. 2023. PMID: 37813647 Free PMC article.
-
Clinical pharmacokinetics of thalidomide.Clin Pharmacokinet. 2004;43(5):311-27. doi: 10.2165/00003088-200443050-00004. Clin Pharmacokinet. 2004. PMID: 15080764 Review.
-
Thalidomide increases human hepatic cytochrome P450 3A enzymes by direct activation of the pregnane X receptor.Chem Res Toxicol. 2014 Feb 17;27(2):304-308. doi: 10.1021/tx4004374. Epub 2014 Feb 5. Chem Res Toxicol. 2014. PMID: 24460184 Free PMC article.
-
Editor's Highlight: Multiparametric Image Analysis of Rat Dorsal Root Ganglion Cultures to Evaluate Peripheral Neuropathy-Inducing Chemotherapeutics.Toxicol Sci. 2017 Mar 1;156(1):275-288. doi: 10.1093/toxsci/kfw254. Toxicol Sci. 2017. PMID: 28115644 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources