Evidence map›Paper›PMID 17511881›Full record

ArticleBreast cancer research : BCR2007

HER2 gene status in primary breast cancers and matched distant metastases.

Coya Tapia, Spasenija Savic, Urs Wagner, René Schönegg, Hedvika Novotny, Bruno Grilli, Michelle Herzog, Audrey Devito Barascud, Inti Zlobec, Gieri Cathomas and 3 more

Abstract read
In one paragraph

Article in Breast cancer research : BCR, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed, 2 pooled it
–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

43 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Guideline
  2. Metastatic breast cancer, version 1.2012: featured updates to the NCCN guidelines.Journal of the National Comprehensive Cancer Network : JNCCN · 2012
    Guideline
  3. Cyclin E1 Expression and Palbociclib Efficacy in Previously Treated Hormone Receptor-Positive Metastatic Breast Cancer.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2019
    Trial
  4. Trial
  5. Trial
  6. Review
  7. Article
  8. Article
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  10. Article
  11. Review
  12. Review
  13. Review
  14. Article
  15. Journal of gastrointestinal oncology · 2017
    Article
  16. Article
  17. BJR case reports · 2017
    Article
  18. Article
  19. Targeting tumor metastases: Drug delivery mechanisms and technologies.Journal of controlled release : official journal of the Controlled Release Society · 2015
    Review
  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

13 authors.

Coya TapiaUniversity Department of Pathology of Basel and Baselland, Institute for Pathology, Schönbeinstrasse 40, Basel, 4003, Switzerland.
Spasenija Savic
Urs Wagner
René Schönegg
Hedvika Novotny
Bruno Grilli
Michelle Herzog
Audrey Devito Barascud
Inti Zlobec
Gieri Cathomas
Luigi Terracciano
Georg Feichter
Lukas Bubendorf

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThe status of the gene encoding human EGF-like receptor 2 (HER2) is an important prognostic and predictive marker in breast cancer. Only breast cancers with HER2 amplification respond to the targeted therapy with trastuzumab. It is controversial to what degree the primary tumour is representative of distant metastases in terms of HER2 status. Discrepancies in HER2 status between primary tumours and distant metastases have been described, but their reasons remain unclear. Here, we compared HER2 status on cytological specimens of distant metastases with the result from the primary carcinomas, and explored the prevalence of and the reasons for discrepant results.

methodsHER2 status was determined by fluorescence in situ hybridisation. HER2 gene amplification was defined as a HER2/chromosome 17 signal ratio of 2 or more. HER2 results from cytological specimens of matched distant metastases were compared with the results from the corresponding primary tumours (n = 105 patients). In addition, lymph node metastases were analysed in 31 of these patients.

resultsHER2 amplification was found in 20% of distant metastases. HER2 status was discordant between the primary tumour and distant metastasis in 7.6% of the 105 patients. Re-evaluation revealed that in five patients (4.7%), discrepancies were due to interpretational difficulties. In two of these patients, focal amplification had initially been overlooked as a result of heterogeneity in the primary tumours or in the metastases, respectively. A further three patients had borderline amplification with a ratio close to 2. Discrepancy remained unexplained in three patients (2.9%).

conclusionHER2 gene status remains highly conserved as breast cancers metastasise. However, discrepant results do occur because of interpretational difficulties and heterogeneity of HER2 amplification. Cytological specimens from distant metastases are well suited for HER2 fluorescence in situ hybridisation analysis.

Indexed as

Genes, erbB-2Breast NeoplasmsErb-b2 Receptor Tyrosine KinasesFemaleGene AmplificationHumansIn Situ Hybridization, FluorescenceLymphatic MetastasisNeoplasm MetastasisOligonucleotide Array Sequence AnalysisErb-b2 Receptor Tyrosine Kinases

Identifiers

PMID17511881
PMCPMC1929093

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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.