Evidence map›Paper›PMID 37120672›Full record

ArticleBritish journal of cancer2023

Anticipating changes in the HER2 status of breast tumours with disease progression-towards better treatment decisions in the new era of HER2-low breast cancers.

Anthony Bergeron, Aurélie Bertaut, Françoise Beltjens, Céline Charon-Barra, Alix Amet, Clémentine Jankowski, Isabelle Desmoulins, Sylvain Ladoire, Laurent Arnould

Open access · hybridAbstract read
In one paragraph

Article in British journal of cancer, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
9.4field-weighted citation impact, top 2% 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

35 citing papers in PubMed, 41 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article
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

9 authors at 2 institutions in 1 country.

Anthony BergeronUnit of Pathology, Department of Biology and Pathology of Tumours, Georges-François Leclerc [Cancer] Centre, 1 rue du Professeur Marion, 21000, Dijon, France. abergeron@cgfl.fr.ORCID http://orcid.org/0000-0001-5757-314X
Aurélie BertautUnit of Methodology and Biostatistics, Georges-François Leclerc [Cancer] Center, 1 rue du Professeur Marion, 21000, Dijon, France.
Françoise BeltjensUnit of Pathology, Department of Biology and Pathology of Tumours, Georges-François Leclerc [Cancer] Centre, 1 rue du Professeur Marion, 21000, Dijon, France.
Céline Charon-BarraUnit of Pathology, Department of Biology and Pathology of Tumours, Georges-François Leclerc [Cancer] Centre, 1 rue du Professeur Marion, 21000, Dijon, France.
Alix AmetDepartment of Surgery, Georges-François Leclerc [Cancer] Center, 1 rue du Professeur Marion, 21000, Dijon, France.
Clémentine JankowskiDepartment of Surgery, Georges-François Leclerc [Cancer] Center, 1 rue du Professeur Marion, 21000, Dijon, France.
Isabelle DesmoulinsDepartment of Medical Oncology, Georges-François Leclerc [Cancer] Center, 1 rue du Professeur Marion, 21000, Dijon, France.
Sylvain LadoireDepartment of Medical Oncology, Georges-François Leclerc [Cancer] Center, 1 rue du Professeur Marion, 21000, Dijon, France.
Laurent ArnouldUnit of Pathology, Department of Biology and Pathology of Tumours, Georges-François Leclerc [Cancer] Centre, 1 rue du Professeur Marion, 21000, Dijon, France.ORCID http://orcid.org/0000-0001-6133-1362
Centre Georges François Leclerc · FRInserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHER2 expression is often negative or low in primary breast cancers (BCs) but its changes with disease progression remain poorly known. We aimed to estimate them between primary and recurrent tumours, and identify predictive factors.

methodsWe compared the HER2 status, and clinical and pathological characteristics by its evolution category (stable or changed), between all primary BCs and matched recurrences registered in our database in 2000-2020 (n = 512).

resultsHER2-low tumours were the most prevalent at diagnosis (44.9%), followed by HER2-negative tumours (39.3%). HER2 status significantly changed in 37.3% of recurrences, mainly of HER2-negative and HER2-low tumours. HER2-negative tumours which relapsed as HER2-low significantly more frequently expressed oestrogen receptors (ER) and recurred later than stably HER2-negative tumours. Changed HER2 status in distant metastases correlated with lower proliferation rates and higher ER expression in primary tumours, and among metastases of hormone receptor-positive (HR+) tumours-with weak progesterone receptor (PR) expression in primary tumours.

conclusionsHER2 status changes with BC progression, with enrichment of HER2-low tumours in advanced stages. The ER+/PR- status, low proliferation index and time to late recurrence correlated with these changes. These findings highlight the need of retesting recurrences, especially of HR + primary tumours, to identify candidates for new anti-HER2 therapies.

Indexed as

Breast NeoplasmsErb-b2 Receptor Tyrosine KinasesBiomarkers, TumorDisease ProgressionFemaleHumansNeoplasm Recurrence, LocalReceptors, EstrogenReceptors, ProgesteroneBiomarkers, TumorErb-b2 Receptor Tyrosine KinasesReceptors, EstrogenReceptors, Progesterone

Identifiers

PMID37120672
PMCPMC10307899
OpenAlexW4367367381

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.