Publication:
Oral gonadotropin-releasing hormone antagonists in the treatment of uterine myomas: a systematic review and network meta-analysis of efficacy parameters and adverse effects

dc.contributor.coauthorTelek, Savcı Bekir
dc.contributor.kuauthorGürbüz, Zeynep Umay
dc.contributor.kuauthorKalafat, Erkan
dc.contributor.kuauthorAta, Mustafa Barış
dc.contributor.kuprofileUndergraduate Student
dc.contributor.kuprofileFaculty Member
dc.contributor.kuprofileFaculty Member
dc.contributor.schoolcollegeinstituteSchool of Medicine
dc.contributor.schoolcollegeinstituteSchool of Medicine
dc.contributor.schoolcollegeinstituteSchool of Medicine
dc.contributor.unitKoç University Hospital
dc.contributor.yokidN/A
dc.contributor.yokid197389
dc.contributor.yokid182910
dc.date.accessioned2024-11-10T00:08:44Z
dc.date.issued2022
dc.description.abstractObjective: The aim of this systematic review is to gather and synthesize evidence regarding the use of oral gonadotrophin-releasing hormone (GnRH) antagonist for the treatment of bleeding associated with uterine myomas. Data Sources: Web of Science, and MEDLINE databases were searched electronically on March 5, 2021, using combinations of the relevant Medical Subject Headings terms and keywords. The search was restricted to the English language and to human studies. Methods of Study Selection: Only randomized controlled trials involving patients with heavy menstrual bleeding associated with uterine myomas treated with different doses of oral nonpeptide GnRH antagonists with or without add-back therapy were included. Studies comparing oral nonpeptide GnRH antagonists with treatments other than placebo were also excluded. Tabulation, Integration, and Results: A total of 5 randomized trials including 2463 women were included in the analyses. Included studies were found to be at low risk of bias. When treatments were compared against placebo, the top 3 treatments for bleeding suppression were elagolix 600 mg, 400 mg, and 200 mg without add-back. Elagolix 600 mg without add-back therapy had a significantly higher risk of amenorrhea than lower doses of elagolix with and without add-back and relugolix as well. Uterine volume changes were more pronounced in therapies without add-back. All treatments were associated with significantly improved quality of life scores, both for myoma symptom-related and overall health-related scores. With the exception of relugolix with high-dose add-back, all treatments significantly increased low-density lipoprotein (LDL) levels. Again, all treatment modalities except for elagolix 200 mg without add-back significantly increased LDL-to-HDL ratio. The increase was highest for treatment without add-back therapy. Conclusion: Oral GnRH antagonists seem to be effective for myoma-associated bleeding and for improving quality of life. The safety profile is acceptable for short-term use, but lipid metabolism is affected. (C) 2022 Published by Elsevier Inc. on behalf of AAGL.
dc.description.indexedbyWoS
dc.description.indexedbyScopus
dc.description.indexedbyPubMed
dc.description.issue5
dc.description.openaccessNO
dc.description.publisherscopeInternational
dc.description.volume29
dc.identifier.doi10.1016/j.jmig.2021.12.011
dc.identifier.eissn1553-4669
dc.identifier.issn1553-4650
dc.identifier.quartileQ1
dc.identifier.scopus2-s2.0-85123004255
dc.identifier.urihttp://dx.doi.org/10.1016/j.jmig.2021.12.011
dc.identifier.urihttps://hdl.handle.net/20.500.14288/16997
dc.identifier.wos797593200012
dc.keywordsAbnormal Uterine Bleeding
dc.keywordsGnRH Analog
dc.keywordsLeiomyomata
dc.keywordsOral GnRH Antagonists
dc.keywordsQuality of Life
dc.keywordsUterine Myoma Elagolix
dc.keywordsFibroids
dc.keywordsLeiomyomas
dc.keywordsManagement
dc.keywordsBurden
dc.keywordsWomen
dc.languageEnglish
dc.publisherElsevier Science Inc
dc.sourceJournal of Minimally Invasive Gynecology
dc.subjectObstetrics
dc.subjectGynecology
dc.titleOral gonadotropin-releasing hormone antagonists in the treatment of uterine myomas: a systematic review and network meta-analysis of efficacy parameters and adverse effects
dc.typeReview
dspace.entity.typePublication
local.contributor.authoridN/A
local.contributor.authorid0000-0003-0658-138X
local.contributor.authorid0000-0003-1106-3747
local.contributor.kuauthorGürbüz, Zeynep Umay
local.contributor.kuauthorKalafat, Erkan
local.contributor.kuauthorAta, Mustafa Barış

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