Evidence map›Paper›PMID 36451043›Full record

ArticleJournal of cancer research and clinical oncology2023

Prognostic effect of HER2 evolution from primary breast cancer to breast cancer metastases.

Sanja Löb, Eva Linsmeier, Saskia-Laureen Herbert, Tanja Schlaiß, Matthias Kiesel, Jörg Wischhusen, Jessica Salmen, Peter Kranke, Anne Quenzer, Florian Kurz and 4 more

Abstract read
In one paragraph

Article in Journal of cancer research and clinical oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Trial
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. HER2-Low Breast Cancer: Now and in the Future.Cancer research and treatment · 2024
    Review
  8. Frontiers in oncology · 2024
    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

14 authors.

Sanja LöbDepartment of Obstetrics and Gynaecology, University of Würzburg, Würzburg, Germany. Loeb_S1@ukw.de.
Eva LinsmeierDepartment of Obstetrics and Gynaecology, University of Würzburg, Würzburg, Germany.
Saskia-Laureen HerbertDepartment of Obstetrics and Gynaecology, University of Würzburg, Würzburg, Germany.
Tanja SchlaißDepartment of Obstetrics and Gynaecology, University of Würzburg, Würzburg, Germany.
Matthias KieselDepartment of Obstetrics and Gynaecology, University of Würzburg, Würzburg, Germany.
Jörg WischhusenDepartment of Obstetrics and Gynaecology, University of Würzburg, Würzburg, Germany.
Jessica SalmenDepartment of Obstetrics and Gynaecology, University of Würzburg, Würzburg, Germany.
Peter KrankeDepartment of Anaesthesia, Critical Care, Emergency and Pain Medicine, University of Würzburg, Würzburg, Germany.
Anne QuenzerDepartment of Obstetrics and Gynaecology, University of Würzburg, Würzburg, Germany.
Florian KurzInstitute of Pathology, University of Würzburg, Würzburg, Germany.
Claire WeissDepartment of Obstetrics and Gynaecology, DRK Klinikum Westend, Berlin, Germany.
Elena Gerhard-HartmannInstitute of Pathology, University of Würzburg, Würzburg, Germany.
Achim WöckelDepartment of Obstetrics and Gynaecology, University of Würzburg, Würzburg, Germany.
Joachim DiessnerDepartment of Obstetrics and Gynaecology, University of Würzburg, Würzburg, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTherapeutic options for breast cancer (BC) treatment are constantly evolving. The Human Epidermal Growth Factor 2 (HER2)-low BC entity is a new subgroup, representing about 55% of all BC patients. New antibody-drug conjugates demonstrated promising results for this BC subgroup. Currently, there is limited information about the conversion of HER2 subtypes between primary tumor and recurrent disease.

methodsThis retrospective study included women with BC at the University Medical Centre Wuerzburg from 1998 to 2021. Data were retrieved from patients' records. HER2 evolution from primary diagnosis to the first relapse and the development of secondary metastases was investigated.

resultsIn the HR-positive subgroup without HER2 overexpression, HER2-low expression in primary BC was 56.7 vs. 14.6% in the triple-negative subgroup (p < 0.000). In the cohort of the first relapse, HER2-low represented 64.1% of HR-positive vs. 48.2% of the triple-negative cohort (p = 0.03). In patients with secondary metastases, HER2-low was 75.6% vs. 50% in the triple negative subgroup (p = 0.10). The subgroup of HER2-positive breast cancer patients numerically increased in the course of disease; the HER2-negative overall cohort decreased. A loss of HER2 expression from primary BC to the first relapse correlated with a better OS (p = 0.018). No clinicopathological or therapeutic features could be identified as potential risk factors for HER2 conversion.

conclusionHER2 expression is rising during the progression of BC disease. In view of upcoming therapeutical options, the re-analysis of newly developed metastasis will become increasingly important.

Indexed as

Breast NeoplasmsNeoplasms, Second PrimaryCutaneous Malignant MelanomaErb-b2 Receptor Tyrosine KinasesFemaleHumansPrognosisRecurrenceRetrospective StudiesErb-b2 Receptor Tyrosine KinasesBreast cancerHER2 conversionHER2-lowHER2 targeted therapyTrastuzumabTrastuzumab deruxtecan

Identifiers

PMID36451043
PMCPMC10349762

What OpenQuestion holds

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LicenceCC BY
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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.