Evidence map›Paper›PMID 34553161›Full record

ArticleF&S reports2021

Efficacy and safety of elagolix with add-back therapy in women with uterine fibroids and coexisting adenomyosis.

Ozgul Muneyyirci-Delale, David F Archer, Charlotte D Owens, Kurt T Barnhart, Linda D Bradley, Eve Feinberg, Veronica Gillispie, Sandra Hurtado, Jin Hee Kim, Alice Wang and 2 more

2 registry-linked trialsOpen access · goldAbstract read
In one paragraph

Article in F&S reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
3.7field-weighted citation impact, top 7% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT02654054 phase3completednot on this map

A Phase 3 Study to Evaluate the Efficacy and Safety of Elagolix in Combination With Estradiol/Norethindrone Acetate for the Management of Heavy Menstrual Bleeding Associated With Uterine Fibroids in Premenopausal Women

TypeinterventionalSponsorAbbVieRan2015 to 2018Enrolled413ConditionsUterine Fibroids, Heavy Menstrual BleedingArmsElagolix, Placebo for Estradiol/Norethindrone Acetate, Estradiol/Norethindrone Acetate, Placebo for Elagolix
NCT02691494 phase3completednot on this map

A Phase 3 Study to Evaluate the Efficacy and Safety of Elagolix in Combination With Estradiol/Norethindrone Acetate for the Management of Heavy Menstrual Bleeding Associated With Uterine Fibroids in Premenopausal Women

TypeinterventionalSponsorAbbVieRan2016 to 2019Enrolled378ConditionsUterine Fibroids, Heavy Menstrual BleedingArmsElagolix, Placebo for Estradiol/Norethindrone Acetate, Estradiol/Norethindrone Acetate, Placebo for Elagolix
3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 21 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 10 institutions in 1 country.

Ozgul Muneyyirci-DelaleDepartment of Obstetrics & Gynecology, State University of New York (SUNY) Downstate Health Sciences University, Brooklyn, New York.
David F ArcherDepartment of Obstetrics & Gynecology, Eastern Virginia Medical School, Norfolk, Virginia.
Charlotte D OwensAbbVie Inc., North Chicago, Illinois.
Kurt T BarnhartDivision of Reproductive Endocrinology and Infertility, Perleman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania.
Linda D BradleyDepartment of Obstetrics & Gynecology, Cleveland Clinic, Cleveland, Ohio.
Eve FeinbergDepartment of Obstetrics & Gynecology, Northwestern University Feinberg School of Medicine, Chicago, Illinois.
Veronica GillispieOchsner Health System, New Orleans, Louisiana.
Sandra HurtadoDepartment of Obstetrics & Gyneocology, University of Texas Health Science Center at Houston, Houston, Texas.
Jin Hee KimDepartment of Obstetrics & Gyneocolgy, Columbia University, New York, New York.
Alice WangAbbVie Inc., North Chicago, Illinois.
Hui WangAbbVie Inc., North Chicago, Illinois.
Elizabeth A StewartDepartments of Obstetrics & Gynecology & Surgery, Mayo Clinic and Mayo Medical School, Rochester, Minnesota.
AbbVie (United States) · USCleveland Clinic · USColumbia University · USEastern Virginia Medical School · USMayo Clinic in Arizona · USNorthwestern University · USOchsner Health System · USState University of New York · USThe University of Texas Health Science Center at Houston · USUniversity of Pennsylvania · US

Funding

AHRQ HHS P50 HS023418
6 · The paper itself

Abstract

objectiveTo determine if coexisting adenomyosis limits the efficacy of elagolix, an oral gonadotropin-releasing hormone antagonist, with hormonal add-back therapy in reducing heavy menstrual bleeding in women with uterine fibroids.

designPooled analysis of two identical, double-blind, randomized, placebo-controlled, 6-month phase 3 trials (Elaris Uterine Fibroids [UF]-1 and UF-2).

settingA total of 153 gynecological clinical care settings in the United States and Canada. PATIENTS: Premenopausal women (18-51 years) with >80 mL of menstrual blood loss (MBL)/cycle and uterine fibroids with and without coexisting adenomyosis diagnosed by ultrasound and/or magnetic resonance imaging at baseline.

interventionsParticipants were randomized 1:1:2 to placebo, elagolix 300 mg twice daily alone, or elagolix 300 mg twice daily with estradiol 1 mg/norethindrone acetate 0.5 mg once daily.

main outcome measuresThe primary endpoint was the proportion of women who had <80 mL of MBL during the final month and ≥50% reduction in MBL from baseline to the final month. Adverse events were monitored.

resultsOf 786 women treated across the two trials, 16% (126 women) had coexisting adenomyosis. Among this subset, a significantly greater proportion of women who received elagolix with add-back therapy (77.1% [95% confidence interval, 66.2, 88.0]) met both primary endpoint criteria compared with women who received placebo (12.2% [95% confidence interval, 1.0, 23.4]). Adverse events most frequently reported in the elagolix with add-back adenomyosis subset were hot flushes (18.3%), nausea (11.7%), and night sweats (8.3%).

conclusionsElagolix with add-back therapy significantly reduced heavy menstrual bleeding in women with uterine fibroids and coexisting adenomyosis, suggesting that elagolix efficacy was not adversely affected by the presence of adenomyosis (Elaris UF-1 and UF-2 Clinical-Trials.gov numbers, NCT02654054 and NCT02691494).

Indexed as

Adenomyosiselagolixuterine fibroids

Identifiers

PMID34553161
PMCPMC8441572
OpenAlexW3164862257

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.