Evidence map›Paper›PMID 42599074›Full record

ReviewReproduction & fertility2026

Role of oral gonadotropin-releasing hormone antagonists in the management of uterine adenomyosis: a narrative review.

Jacques Donnez, Olivier Donnez, Hugh S Taylor, Felice Petraglia, Andrew W Horne, Christian M Becker, Stefan P Renner, Marionna Rius, Elke Bestel, Christina Anna Stratopoulou and 1 more

Abstract readReview
In one paragraph

Review in Reproduction & fertility, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

11 authors.

Jacques DonnezDepartment of Gynecology, Université Catholique de Louvain , Brussels, Belgium.ORCID 0000-0003-2528-206X
Olivier DonnezCentre de l'Endométriose Complexe, Chirurgie Endoscopique Pelvienne, Polyclinique Urbain V (ELSAN Group) , Avignon, France.
Hugh S TaylorDepartment of Obstetrics, Gynecology and Reproductive Sciences, Yale School of Medicine , New Haven, Connecticut, USA.
Felice PetragliaObstetrics and Gynecology Unit, Department of Clinical Experimental and Biomedical Sciences, University of Florence , Florence, Italy.
Andrew W HorneEXPPECT Edinburgh Centre for Reproductive Health, University of Edinburgh , Edinburgh, UK.ORCID 0000-0002-9656-493X
Christian M BeckerEndometriosis CaRe Centre, Nuffield Department of Obstetrics and Gynaecology, University of Oxford , Oxford, UK.
Stefan P RennerDepartment of Gynecology and Obstetrics, Hospital Böblingen , Sindelfingen, Germany.
Marionna RiusEndometriosis Unit, Hospital Clinic of Barcelona, University of Barcelona , Barcelona, Spain.
Elke BestelDepartment of Medical Affairs, Theramex , London, UK.
Christina Anna StratopoulouGynecology Research Laboratory, Institut de Recherche Expérimentale et Clinique, Department of Gynecology, Université Catholique de Louvain , Brussels, Belgium.
Marie-Madeleine DolmansGynecology Research Laboratory, Institut de Recherche Expérimentale et Clinique, Department of Gynecology, Université Catholique de Louvain , Brussels, Belgium.ORCID 0000-0002-6331-3026

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

abstractIn women with uterine adenomyosis, bleeding and pain can have a major impact on quality of life. There is clearly a widespread demand for effective long-term medical therapies. The objective of this narrative review was to investigate the efficacy of oral gonadotropin-releasing hormone (GnRH) antagonists in the management of uterine adenomyosis by analyzing data from two post hoc analyses of two prospective randomized trials (elagolix and relugolix), one retrospective study (relugolix) and one prospective study (linzagolix). All three GnRH oral antagonists were able to control the disease and uterine fibroid-related heavy menstrual bleeding, enhancing quality of life. When administered without add-back therapy, high doses of GnRH antagonists were found to significantly and rapidly reduce uterine volume and the severity of adenomyotic lesions. Nevertheless, some limitations should be addressed. The post hoc analyses were a retrospective look at two prospective randomized clinical trials. In the elagolix study, most women underwent both transvaginal ultrasound and magnetic resonance imaging (MRI). Some who opted out of MRI may have had concurrent adenomyosis that was undetected by ultrasound, so they were not included in the adenomyosis subset. In the relugolix study, baseline ultrasounds were not specifically performed to spot adenomyosis that may have been overlooked in case of large fibroids, as shadowing can partially or completely obscure the disease. While the linzagolix study is prospective and evaluates data from women with proven adenomyosis documented by MRI, the number of cases is limited and randomized controlled trials are needed to confirm and validate this concept. LAY SUMMARY: Uterine adenomyosis is characterized by the presence of endometrial glands inside the myometrium, the muscular layer of the uterus. Transvaginal ultrasound and magnetic resonance imaging now facilitate its diagnosis. The estimated prevalence of adenomyosis among patients of reproductive age is 20-30%. Rising rates in younger patients combined with a growing trend to postpone first pregnancy underscore the importance of understanding the mechanisms behind its development. We need novel strategies for the treatment of typical but distressing symptoms of adenomyosis, which include pelvic pain, abnormal uterine bleeding, menstrual cramps, painful sex and infertility. There is a lack of approved pharmacological agents specifically indicated for the treatment of adenomyosis, presenting a clear unmet need in this population. Oral gonadotropin-releasing hormone (GnRH) antagonists have recently emerged as a promising new therapeutic option. Their advantages over GnRH agonist depot formulations include an absence of the flare-up effect, hence avoiding initially worsening symptoms and rapid reversibility.

Indexed as

AdenomyosisGonadotropin-Releasing HormoneHormone AntagonistsAdministration, OralFemaleHumansHydrocarbons, FluorinatedPhenylurea CompoundsPyrimidinesPyrimidinoneselagolixGonadotropin-Releasing HormoneHormone AntagonistsHydrocarbons, FluorinatedPhenylurea CompoundsPyrimidinesPyrimidinonesrelugolixadenomyosiselagolixGnRH antagonistheavy menstrual bleedinglinzagolixpainquality of liferelugolix

Identifiers

PMID42599074
PMCPMC13548114

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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 Socratic graph.