The potential role of elagolix for treating uterine bleeding associated to uterine myomas

被引:14
|
作者
Barra, Fabio [1 ,2 ]
Vitale, Salvatore Giovanni [3 ]
Seca, Marta [1 ,2 ]
Scala, Carolina [4 ]
Maggiore, Umberto Leone Roberti [5 ]
Cianci, Antonio [3 ]
Ferrero, Simone [1 ,2 ]
机构
[1] IRCCS Osped Policlin San Martino, Acad Unit Obstet & Gynaecol, Genoa, Italy
[2] Univ Genoa, Dept Neurosci Rehabil Ophthalmol Genet Maternal &, Genoa, Italy
[3] Univ Catania, Dept Gen Surg & Med Surg Specialties, Obstet & Gynecol Unit, Catania, Italy
[4] Gaslini Inst, Unit Obstet & Gynecol, Genoa, Italy
[5] IRCCS Natl Canc Inst, Dept Gynecol Oncol, Milan, Italy
关键词
Uterine leiomyomas; uterine fibroids; GNRH antagonist; hormonal therapy; elagolix; elagolix sodium; abnormal uterine bleeding; heavy menstrual bleeding; ULIPRISTAL ACETATE; GNRH ANTAGONIST; FIBROIDS; ENDOMETRIOSIS; LEIOMYOMAS; MANAGEMENT; STEROIDS; AGONISTS; GROWTH; CELLS;
D O I
10.1080/14656566.2020.1755254
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction Uterine myomas represents a widespread gynecological disease of women in reproductive age. Although surgery remains the first choice for treating most patients, in the last years, new medical approaches have been considered in order to ameliorate heavy menstrual bleeding (HMB) related to their presence. Elagolix is a second-generation gonadotropin-releasing hormone (GnRH) antagonist under investigation for the long-term treatment of uterine myomas. Areas covered The aim of this drug evaluation is to give a complete overview of pharmacokinetic and pharmacodynamic data on elagolix for treating HMB related to uterine myomas and to report the results of the current clinical trials in this setting. Expert opinion In two previous phase II studies, this drug succeeded in ameliorating blood loss and quality of life of patients affected by uterine myomas with a good safety profile. Three phase III trials (ELARIS UF-I, UF-II, and EXTEND) investigated the efficacy, tolerability, and safety of elagolix at 300 mg twice daily with add-back therapy. The primary endpoint, consisting in the reduction in HMB compared to placebo, was met in the majority of patients under treatment. Currently, elagolix is under investigation in two other ongoing multicenter phase III clinical studies.
引用
收藏
页码:1419 / 1430
页数:12
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