Evidence map›Paper›PMID 35584336›Full record

Trial reportJournal of clinical oncology : official journal of the American Society of Clinical Oncology2022

Elacestrant (oral selective estrogen receptor degrader) Versus Standard Endocrine Therapy for Estrogen Receptor-Positive, Human Epidermal Growth Factor Receptor 2-Negative Advanced Breast Cancer: Results From the Randomized Phase III EMERALD Trial.

Francois-Clement Bidard, Virginia G Kaklamani, Patrick Neven, Guillermo Streich, Alberto J Montero, Frédéric Forget, Marie-Ange Mouret-Reynier, Joo Hyuk Sohn, Donatienne Taylor, Kathleen K Harnden and 19 more

Erratum issued Registry-linked trialOpen access · hybridAbstract readClinical Trial, Phase IIIRandomized Controlled Trial
In one paragraph

Trial report in Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. It is linked to trial NCT06201234 (Phase II Study Evaluating the Addition of Elacestrant, an Oral Selective Estrogen Receptor Degrader), which is not on this map. Cited by 416 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
416citing papers in PubMed, 5 pooled it
90.4field-weighted citation impact, top 1% 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.

NCT06201234 phase2recruitingnot on this mapstarted 2024, after this paper: background citation

Phase II Study Evaluating the Addition of Elacestrant, an Oral Selective Estrogen Receptor Degrader (SERD), to Standard-of-care Olaparib in Patients With Hormone Receptor (HR)-Positive, HER2-negative Locally Advanced or Metastatic Breast Cancer With gBRCA1/2 Mutations

TypeinterventionalSponsorGBG Forschungs GmbHRan2024 to 2028Enrolled176ConditionsHormone Receptor Positive HER-2 Negative Breast Cancer, Advanced or Metastatic Breast Cancer, BRCA1 Mutation, BRCA2 MutationArmsOlaparib + Elacestrant, Olaparib
3 · Its place in the literature

Who cites it

416 citing papers in PubMed, 5 syntheses or guidelines pooled it, 643 citations in OpenAlex.

  1. Guideline
  2. Guideline
  3. The Role of Estrogen Receptor-Targeted PET with 16α-Journal of nuclear medicine : official publication, Society of Nuclear Medicine · 2026
    Pooled it
  4. Pooled it
  5. Guideline
  6. Trial
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  9. Pembrolizumab and Paclitaxel in Patients with HR+/HER2- Breast Cancer with HER2-Enriched or Basal-like Subtypes.Clinical cancer research : an official journal of the American Association for Cancer Research · 2026
    Trial
  10. Imlunestrant with or without abemaciclib in advanced breast cancer: updated efficacy results from the phase III EMBER-3 trial.Annals of oncology : official journal of the European Society for Medical Oncology · 2026
    Trial
  11. Trial
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  19. A Phase II Study of Fulvestrant plus Abemaciclib in Hormone Receptor-Positive Advanced or Recurrent Endometrial Cancer.Clinical cancer research : an official journal of the American Association for Cancer Research · 2025
    Trial
  20. Trial

356 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

29 authors at 20 institutions in 10 countries.

Francois-Clement BidardInstitut Curie, Paris and Saint Cloud, France.
Virginia G KaklamaniUniversity of Texas Health Sciences Center, San Antonio, TX.ORCID 0000-0002-3313-8458
Patrick NevenUniversitaire Ziekenhuizen (UZ)-Leuven Cancer Institute, Leuven, Belgium.
Guillermo StreichCentro Médico Austral, Buenos Aires, Argentina.
Alberto J MonteroUniversity Hospitals Seidman Cancer Center-Case Western Reserve University, Cleveland, OH.ORCID 0000-0002-8221-8120
Frédéric ForgetCentre Hospitalier de l'Ardenne-Site de Libramont, Libramont-Chevigny, Belgium.
Marie-Ange Mouret-ReynierCentre Jean Perrin, Clermont-Ferrand, France.
Joo Hyuk SohnYonsei Cancer Center, Yonsei University Health System-Medical Oncology, Seoul, Republic of Korea.ORCID 0000-0002-2303-2764
Donatienne TaylorUniversité catholique de Louvain, CHU UCL Namur-Site Sainte-Elisabeth, Namur, Belgium.ORCID 0000-0002-5141-513X
Kathleen K HarndenInova Schar Cancer Institute, Fairfax, Virginia.ORCID 0000-0002-8211-708X
Hung KhongMoffit Cancer Center & Research Institute, Tampa, FL.ORCID 0000-0001-8365-957X
Judit KocsisBács-Kiskun Megyei Kórház, Kecskemét, Hungary.
Florence DalencInstitut Claudius Regaud, IUCT-Oncopole, Toulouse, France.
Patrick M DillonUniversity of Virginia Cancer Center, Charlottesville, VA.ORCID 0000-0003-0622-725X
Sunil BabuFort Wayne Medical Oncology and Hematology, Fort Wayne, IN.
Simon WatersVelindre Cancer Centre, Cardiff, United Kingdom.ORCID 0000-0003-0205-4398
Ines DeleuAZ Nikolaas, Sint-Niklaas, Belgium.
José A García SáenzInstituto de Investigación Sanitaria Hospital Clinico San Carlos (IdISSC), Madrid, Spain.
Emilio BriaFondazione Policlinico Universitario Agostino Gemelli IRCCS, Università Cattolica del Sacro Cuore, Roma, Italy.ORCID 0000-0002-2333-704X
Marina CazzanigaOspedale San Gerardo-ASST Monza, Monza, Italy.ORCID 0000-0003-1756-6935
Janice LuUniversity of Southern California/Norris Comprehensive Cancer Center, Los Angeles, CA.
Philippe AftimosInstitut Jules Bordet - Université Libre de Bruxelles, Brussels, Belgium.ORCID 0000-0001-9946-4726
Javier CortésInternational Breast Cancer Center (IBCC), Quironsalud Group, Barcelona, Spain.ORCID 0000-0001-7623-1583
Shubin LiuCytel, Waltham, MA.
Giulia ToniniMenarini Group, Florence, Italy.
Dirk LaurentBerlin Chemie AG/Menarini Group, Berlin, Germany.
Nassir HabboubiStemline Therapeutics/Menarini Group, New York, NY.
Maureen G ConlanRadius Health, Inc, Boston, MA.
Aditya BardiaMassachusetts General Hospital Cancer Center, Harvard Medical School, Boston, MA.ORCID 0000-0003-4885-1157
Azienda Ospedaliera San Gerardo · ITBács-Kiskun Megyei Kórház · HUCentre Jean Perrin · FRCytel (United States) · USFort Wayne Medical Institute · USHarvard University · USInstitut Claudius Regaud · FRInstituto de Investigación Sanitaria del Hospital Clínico San Carlos · ESLibreville Hospital · GAMedSIR (Spain) · ESMenarini Group (Germany) · DEMenarini Group (Italy) · ITMoffitt Cancer Center · USRadius Health (United States) · USThe University of Texas Health Science Center at San Antonio · USUCLouvain · BEUniversità Cattolica del Sacro Cuore · ITUniversitair Ziekenhuis Leuven · BEUniversité de Versailles Saint-Quentin-en-Yvelines · FRUniversité Libre de Bruxelles · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposePatients with pretreated estrogen receptor (ER)-positive/human epidermal growth factor receptor 2 (HER2)-negative advanced breast cancer have poor prognosis. Elacestrant is a novel, oral selective ER degrader that demonstrated activity in early studies.

methodsThis randomized, open-label, phase III trial enrolled patients with ER-positive/HER2-negative advanced breast cancer who had one-two lines of endocrine therapy, required pretreatment with a cyclin-dependent kinase 4/6 inhibitor, and ≤ 1 chemotherapy. Patients were randomly assigned to elacestrant 400 mg orally once daily or standard-of-care (SOC) endocrine monotherapy. Primary end points were progression-free survival (PFS) by blinded independent central review in all patients and patients with detectable

resultsPatients were randomly assigned to elacestrant (n = 239) or SOC (n = 238).

conclusionElacestrant is the first oral selective ER degrader demonstrating a significant PFS improvement versus SOC both in the overall population and in patients with

Indexed as

Breast NeoplasmsAntineoplastic Combined Chemotherapy ProtocolsCyclin-Dependent Kinase 4Erb-b2 Receptor Tyrosine KinasesEstrogen AntagonistsFemaleHumansReceptors, EstrogenTetrahydronaphthalenesCyclin-Dependent Kinase 4elacestrantERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesEstrogen AntagonistsReceptors, EstrogenTetrahydronaphthalenes

Identifiers

PMID35584336
PMCPMC9553388
OpenAlexW4280490473

What OpenQuestion holds

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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.