Literature DB >> 9429742

Absolute bioavailability of letrozole in healthy postmenopausal women.

A Sioufi1, N Gauducheau, V Pineau, F Marfil, A Jaouen, J M Cardot, J Godbillon, C Czendlik, H Howald, C Pfister, F Vreeland.   

Abstract

Letrozole is a new non-steroidal inhibitor of the aromatase enzyme system. It is currently under development for the treatment of postmenopausal women with advanced breast cancer. Absolute bioavailability of letrozole when given orally as one 2.5 mg film-coated tablet in comparison to the same dose given intravenously as a bolus injection was studied in 12 healthy postmenopausal women. Letrozole absolute systemic bioavailability after p.o. administration was 99.9 +/- 16.3%. Elimination of letrozole was slow. Total-body clearance of letrozole from plasma after i.v. administration was low (2.21 L h-1). The calculated distribution volume at steady state (1.87 L kg-1) suggests a rather high tissue distribution. Biotransformation of letrozole is the main elimination mechanism with the glucuronide conjugate of the secondary alcohol metabolite being the predominant species found in urine. The two study treatments were tolerated equally well.

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Year:  1997        PMID: 9429742     DOI: 10.1002/(sici)1099-081x(199712)18:9<779::aid-bdd64>3.0.co;2-5

Source DB:  PubMed          Journal:  Biopharm Drug Dispos        ISSN: 0142-2782            Impact factor:   1.627


  25 in total

1.  Pharmacokinetics of finrozole (MPV-2213ad), a novel selective aromatase inhibitor, in healthy men.

Authors:  O Ahokoski; K Irjala; M Taalikka; P Manninen; K Halonen; L Kangas; E Salminen; R Huupponen; H Scheinin
Journal:  Br J Clin Pharmacol       Date:  2001-12       Impact factor: 4.335

Review 2.  Clinical pharmacokinetics of aromatase inhibitors and inactivators.

Authors:  Per Lønning
Journal:  Clin Pharmacokinet       Date:  2003       Impact factor: 6.447

Review 3.  Effects of food on the clinical pharmacokinetics of anticancer agents: underlying mechanisms and implications for oral chemotherapy.

Authors:  Brahma N Singh; Bimal K Malhotra
Journal:  Clin Pharmacokinet       Date:  2004       Impact factor: 6.447

Review 4.  The role of aromatase inhibitors in ameliorating deleterious effects of ovarian stimulation on outcome of infertility treatment.

Authors:  Mohamed F M Mitwally; Robert F Casper; Michael P Diamond
Journal:  Reprod Biol Endocrinol       Date:  2005-10-04       Impact factor: 5.211

5.  Population pharmacokinetic analysis of letrozole in Japanese postmenopausal women.

Authors:  Hiromi Tanii; Yoshihisa Shitara; Toshiharu Horie
Journal:  Eur J Clin Pharmacol       Date:  2011-04-15       Impact factor: 2.953

6.  Synthesis and PET studies of [(11)C-cyano]letrozole (Femara), an aromatase inhibitor drug.

Authors:  Kun-Eek Kil; Anat Biegon; Yu-Shin Ding; Andre Fischer; Richard A Ferrieri; Sung Won Kim; Deborah Pareto; Michael J Schueller; Joanna S Fowler
Journal:  Nucl Med Biol       Date:  2009-02       Impact factor: 2.408

Review 7.  Aromatase inhibitors and inactivators for breast cancer therapy.

Authors:  Per E Lønning
Journal:  Drugs Aging       Date:  2002       Impact factor: 3.923

8.  Profound reduction of ovarian estrogen by aromatase inhibition in obese women.

Authors:  Lauren A Ross; Alex J Polotsky; Alexander Kucherov; Andrew P Bradford; Jennifer Lesh; Justin Chosich; Nancy Gee; Nanette Santoro
Journal:  Obesity (Silver Spring)       Date:  2014-02-18       Impact factor: 5.002

9.  Inactivation of CYP2A6 by the Dietary Phenylpropanoid trans-Cinnamic Aldehyde (Cinnamaldehyde) and Estimation of Interactions with Nicotine and Letrozole.

Authors:  Jeannine Chan; Tyler Oshiro; Sarah Thomas; Allyson Higa; Stephen Black; Aleksandar Todorovic; Fawzy Elbarbry; John P Harrelson
Journal:  Drug Metab Dispos       Date:  2016-02-05       Impact factor: 3.922

Review 10.  Letrozole. A review of its use in postmenopausal women with advanced breast cancer.

Authors:  H M Lamb; J C Adkins
Journal:  Drugs       Date:  1998-12       Impact factor: 9.546

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