Treatment of symptomatic uterine leiomyoma with letrozole

dc.contributor.authorGurates, Bilgin
dc.contributor.authorParmaksiz, Cem
dc.contributor.authorKilic, Gokhan
dc.contributor.authorCelik, Husnu
dc.contributor.authorKumru, Selahattin
dc.contributor.authorSimsek, Mehmet
dc.date.accessioned2026-08-12T17:45:26Z
dc.date.issued2008
dc.departmentFırat Üniversitesi
dc.description.abstractUterine leiomyomas are the most common benign tumours of the female genital tract, often necessitating hysterectomy. The most common symptoms are dysmenorrhoea, menorrhagia, infertility and abortion. Ovarian hormones seem to play an essential role in pathogenesis, and deprivation of ovarian oestrogen causes leiomyomas to shrink significantly. The purpose of this study was to evaluate the effects of the non-steroidal aromatase inhibitor letrozole on uterine leiomyomas and on bone metabolism. A prospective, open clinical trial was conducted in a university-based hospital. Sixteen premenopausal women with symptomatic uterine leiomyomas were treated with letrozole 5 mg/day orally for 3 months. The main outcome measures of uterine and uterine leiomyoma sizes, serum FSH, LH, oestradiol concentrations, ovarian volumes and myoma-related symptoms were noted at baselines and once a month during treatment. Lumbar spine bone mineral density and biochemical markers of bone metabolism were studied at the beginning and at the end of 3 months. Letrozole significantly decreased uterine leiomyoma sizes (P < 0.01) and promptly benefited women with heavy menstrual bleeding associated with leiomyomas without changing bone mineral density. Aromatase inhibitors may represent a new generation of medications for the treatment of leiomyoma and associated symptoms. Larger clinical trials are needed, however, to fully evaluate their safety and efficacy.
dc.description.sponsorshipFirat University [2003-5-33]
dc.description.sponsorshipThe authors thank Professor Serdar E Bulun for his critical review of the manuscript. This work was supported by the Firat University research grant 2003-5-33 (to BG).
dc.identifier.doi10.1016/S1472-6483(10)60246-5
dc.identifier.endpage574
dc.identifier.issn1472-6483
dc.identifier.issn1472-6491
dc.identifier.issue4
dc.identifier.orcid0000-0002-7926-7458
dc.identifier.pmid18854113
dc.identifier.scopus2-s2.0-54449086371
dc.identifier.scopusqualityQ1
dc.identifier.startpage569
dc.identifier.urihttps://doi.org/10.1016/S1472-6483(10)60246-5
dc.identifier.urihttps://hdl.handle.net/11508/60668
dc.identifier.volume17
dc.identifier.wosWOS:000259829800017
dc.identifier.wosqualityQ1
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherElsevier Sci Ltd
dc.relation.ispartofReproductive Biomedicine Online
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/openAccess
dc.snmzKA_WoS_20260511
dc.subjectaromatase inhibitor
dc.subjectbone density/metabolism
dc.subjectmyoma
dc.subjectoestrogen
dc.subjectuterine leiomyomata
dc.titleTreatment of symptomatic uterine leiomyoma with letrozole
dc.typeArticle

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