Evidence map›Paper›PMID 36806375›Full record

ReviewESMO open2023

How I treat endocrine-dependent metastatic breast cancer.

A Gombos, A Goncalves, G Curigliano, R Bartsch, J A Kyte, M Ignatiadis, A Awada

Open access · goldAbstract readReview
In one paragraph

Review in ESMO open, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
5.7field-weighted citation impact, top 4% 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.

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

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 22 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Review
  5. Article
  6. Review
  7. Article
  8. Exploring the real-world experience of abemaciclib treatment for HR +, HER2 - metastatic breast cancer-a qualitative analysis of the IMPACTOR study.Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer · 2025
    Article
  9. Article
  10. Adjuvant CDK4/6 inhibitors in hormone receptor-positive early breast cancer: one fits all?Translational breast cancer research : a journal focusing on translational research in breast cancer · 2024
    Article
  11. Review
  12. Observational
  13. Review
  14. Male Breast Cancer: Current Scenario and Future Perspectives.Technology in cancer research & treatment
    Review
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

7 authors at 5 institutions in 5 countries.

A GombosDepartment of Medical Oncology Institut Jules Bordet, Université Libre de Bruxelles, Brussels, Belgium.
A GoncalvesInstitut Paoli Calmettes, Centre de Recherche en Cancérologie de Marseille (CRCM), Inserm U1068, CNRS U7258, Aix Marseille University, Marseille, France.
G CuriglianoEuropean Institute of Oncology, University of Milano, Milano, Italy.
R BartschDepartment of Medicine I, Medical University of Vienna, Vienna, Austria.
J A KyteDepartment of Oncology, Oslo University Hospital, Oslo, Norway.
M IgnatiadisDepartment of Medical Oncology Institut Jules Bordet, Université Libre de Bruxelles, Brussels, Belgium.
A AwadaDepartment of Medical Oncology Institut Jules Bordet, Université Libre de Bruxelles, Brussels, Belgium. Electronic address: ahmad.awada@bordet.be.
Université Libre de Bruxelles · BECentre National de la Recherche Scientifique · FRMedical University of Vienna · ATOslo University Hospital · NOUniversity of Milan · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Estrogen receptor-positive (ER+)/HER2-negative (HER2-), the so-called luminal-type breast cancer, is the most frequent subset, accounting for around 70% of all breast cancer cases. Endocrine therapy (ET) combined with cyclin-dependent kinases (CDK) 4/6 inhibitors is the standard first option in the management of advanced luminal breast cancer independently of disease extension. Classically, patients undergo multiple lines of ET ± targeted treatments until endocrine resistance occurs and palliative chemotherapy is proposed. Understanding endocrine resistance mechanisms and development of novel ET options is one of the main challenges in current clinical research. Another area of utmost interest is the improvement of post-endocrine therapeutic approaches. Among others, the development of antibody-drug conjugates (ADCs) is very promising, and some of these drugs will probably soon become a part of the therapeutic arsenal against this incurable disease. This review paper provides an overview of currently available treatment options in ER+/HER2- metastatic breast cancer and extensively discusses new approaches in late clinical development.

Indexed as

Breast NeoplasmsMolecular Targeted TherapyAntineoplastic AgentsDrug Resistance, NeoplasmFemaleHumansImmunoconjugatesMutationSelective Estrogen Receptor ModulatorsAntineoplastic AgentsImmunoconjugatesSelective Estrogen Receptor Modulatorsantibody–drug conjugate (ADC)CDK 4/6luminal breast cancerPIK3CASERD

Identifiers

PMID36806375
PMCPMC9969253
OpenAlexW4321180784

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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 OpenQuestion graph.