Evidence map›Paper›PMID 29666928›Full record

ReviewCurrent treatment options in oncology2018

Implications of ESR1 Mutations in Hormone Receptor-Positive Breast Cancer.

Tomás Reinert, Rodrigo Gonçalves, José Bines

Abstract readReview
PubMed Publisher
In one paragraph

Review in Current treatment options in oncology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
5.2field-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

23 citing papers in PubMed, 41 citations in OpenAlex.

  1. Review
  2. A Novel Sensitive Technique to DetectCancer innovation · 2026
    Article
  3. Review
  4. Article
  5. Unveiling the Bioactive Efficacy ofPharmaceuticals (Basel, Switzerland) · 2024
    Article
  6. Review
  7. Cancers · 2023
    Review
  8. Review
  9. Review
  10. Review
  11. Article
  12. Article
  13. Review
  14. Proteolysis-targeting chimeras and their implications in breast cancer.Exploration of targeted anti-tumor therapy · 2021
    Review
  15. Article
  16. Article
  17. Detection ofFrontiers in oncology · 2020
    Review
  18. Article
  19. Article
  20. 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

3 authors at 3 institutions in 1 country.

Tomás ReinertHospital do Câncer Mãe de Deus, Porto Alegre, Brazil.
Rodrigo GonçalvesSetor de Mastologia, Hospital das Clínicas, Disciplina de Ginecologia, Departamento de Obstetrícia e Ginecologia, Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brazil.
José BinesInstituto Nacional de Câncer (INCA-HCIII), Rua Visconde de Santa Isabel 274 - oitavo andar, Rio de Janeiro, Brazil. jose_bines@yahoo.com.
Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo · BRHospital do Câncer III · BRHospital Mãe de Deus · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

opinion statementEndocrine treatment resistance eventually develops during adjuvant and even more often during hormonal treatment for advanced breast cancer (ABC). An ESR1 gene mutation, which encodes for the estrogen receptor (ER) protein, is one of the potential mechanisms of therapy resistance. The ESR1 mutations result in conformational changes in the ER leading to subsequent estrogen-independent transcriptional activity. These mutations are found at a lower level in early stage when compared to metastatic BC, more often through selective pressure after aromatase inhibitor (AI) treatment. Recent studies have explored the role of ESR1 mutations as potential prognostic and predictive biomarkers and showed that ESR1 mutations are likely associated with a more aggressive disease. However, definitive associations with outcome in order to make a specific treatment recommendation are yet to be found. The development of targeted therapy directed to ESR1-mutated clones is an appealing concept, and preclinical and clinical works are in progress. ESR1 mutations represent an exciting field with a rapidly increasing number of recent publications that will likely advance the knowledge of treatment resistance mechanisms and pave the way into more individualized patient endocrine treatment.

Indexed as

PrognosisAromatase InhibitorsBiomarkers, TumorBreast NeoplasmsDrug Resistance, NeoplasmEstrogen Receptor alphaFemaleHumansMutationAromatase InhibitorsBiomarkers, TumorESR1 protein, humanEstrogen Receptor alphaAromatase inhibitorsBreast cancerEndocrine therapyESR1ESR1 mutations

Identifiers

PMID29666928
OpenAlexW2801511066

What OpenQuestion 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 OpenQuestion graph.