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Elagolix for Heavy Menstrual Bleeding in Women with Uterine Fibroids.

Authors :
Schlaff, William D.
Ackerman, Ronald T.
Al-Hendy, Ayman
Archer, David F.
Barnhart, Kurt T.
Bradley, Linda D.
Carr, Bruce R.
Feinberg, Eve C.
Hurtado, Sandra M.
JinHee Kim
Ran Liu
Mabey Jr., R. Garn
Owens, Charlotte D.
Poindexter, Alfred
Puscheck, Elizabeth E.
Rodriguez-Ginorio, Henry
Simon, James A.
Soliman, Ahmed M.
Stewart, Elizabeth A.
Watts, Nelson B.
Source :
New England Journal of Medicine. 1/23/2020, Vol. 382 Issue 4, p328-340. 13p.
Publication Year :
2020

Abstract

<bold>Background: </bold>Uterine fibroids are hormone-responsive neoplasms that are associated with heavy menstrual bleeding. Elagolix, an oral gonadotropin-releasing hormone antagonist resulting in rapid, reversible suppression of ovarian sex hormones, may reduce fibroid-associated bleeding.<bold>Methods: </bold>We conducted two identical, double-blind, randomized, placebo-controlled, 6-month phase 3 trials (Elaris Uterine Fibroids 1 and 2 [UF-1 and UF-2]) to evaluate the efficacy and safety of elagolix at a dose of 300 mg twice daily with hormonal "add-back" therapy (to replace reduced levels of endogenous hormones; in this case, estradiol, 1 mg, and norethindrone acetate, 0.5 mg, once daily) in women with fibroid-associated bleeding. An elagolix-alone group was included to assess the impact of add-back therapy on the hypoestrogenic effects of elagolix. The primary end point was menstrual blood loss of less than 80 ml during the final month of treatment and at least a 50% reduction in menstrual blood loss from baseline to the final month; missing data were imputed with the use of multiple imputation.<bold>Results: </bold>A total of 412 women in UF-1 and 378 women in UF-2 underwent randomization, received elagolix or placebo, and were included in the analyses. Criteria for the primary end point were met in 68.5% of 206 women in UF-1 and in 76.5% of 189 women in UF-2 who received elagolix plus add-back therapy, as compared with 8.7% of 102 women and 10% of 94 women, respectively, who received placebo (P<0.001 for both trials). Among the women who received elagolix alone, the primary end point was met in 84.1% of 104 women in UF-1 and in 77% of 95 women in UF-2. Hot flushes (in both trials) and metrorrhagia (in UF-1) occurred significantly more commonly with elagolix plus add-back therapy than with placebo. Hypoestrogenic effects of elagolix, especially decreases in bone mineral density, were attenuated with add-back therapy.<bold>Conclusions: </bold>Elagolix with add-back therapy was effective in reducing heavy menstrual bleeding in women with uterine fibroids. (Funded by AbbVie; Elaris UF-1 and Elaris UF-2 ClinicalTrials.gov numbers, NCT02654054 and NCT02691494.). [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00284793
Volume :
382
Issue :
4
Database :
Academic Search Index
Journal :
New England Journal of Medicine
Publication Type :
Academic Journal
Accession number :
141444743
Full Text :
https://doi.org/10.1056/NEJMoa1904351