Evidence map›Paper›PMID 28752092›Full record

Trial reportBioMed research international2017

Automated Image Analysis of HER2 Fluorescence In Situ Hybridization to Refine Definitions of Genetic Heterogeneity in Breast Cancer Tissue.

Gedmante Radziuviene, Allan Rasmusson, Renaldas Augulis, Daiva Lesciute-Krilaviciene, Aida Laurinaviciene, Eduard Clim, Arvydas Laurinavicius

Open access · hybridAbstract readClinical Trial
In one paragraph

Trial report in BioMed research international, 2017. 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
0.9field-weighted citation impact, top 23% 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

8 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Automatic quantification ofJournal of medical imaging (Bellingham, Wash.) · 2019
    Article
  7. Article
  8. Oncotarget · 2018
    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

7 authors at 1 institution in 1 country.

Gedmante RadziuvieneNational Center of Pathology, Affiliate of Vilnius University Hospital Santariskiu Clinics, P. Baublio 5, LT-08406 Vilnius, Lithuania.
Allan RasmussonNational Center of Pathology, Affiliate of Vilnius University Hospital Santariskiu Clinics, P. Baublio 5, LT-08406 Vilnius, Lithuania.
Renaldas AugulisNational Center of Pathology, Affiliate of Vilnius University Hospital Santariskiu Clinics, P. Baublio 5, LT-08406 Vilnius, Lithuania.
Daiva Lesciute-KrilavicieneNational Center of Pathology, Affiliate of Vilnius University Hospital Santariskiu Clinics, P. Baublio 5, LT-08406 Vilnius, Lithuania.
Aida LaurinavicieneNational Center of Pathology, Affiliate of Vilnius University Hospital Santariskiu Clinics, P. Baublio 5, LT-08406 Vilnius, Lithuania.
Eduard ClimTissueGnostics, Vienna, Austria.
Arvydas LaurinaviciusNational Center of Pathology, Affiliate of Vilnius University Hospital Santariskiu Clinics, P. Baublio 5, LT-08406 Vilnius, Lithuania.ORCID 0000-0001-9232-1730
Vilnius University · LT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Human epidermal growth factor receptor 2 gene- (HER2-) targeted therapy for breast cancer relies primarily on HER2 overexpression established by immunohistochemistry (IHC) with borderline cases being further tested for amplification by fluorescence in situ hybridization (FISH). Manual interpretation of HER2 FISH is based on a limited number of cells and rather complex definitions of equivocal, polysomic, and genetically heterogeneous (GH) cases. Image analysis (IA) can extract high-capacity data and potentially improve HER2 testing in borderline cases. We investigated statistically derived indicators of HER2 heterogeneity in HER2 FISH data obtained by automated IA of 50 IHC borderline (2+) cases of invasive ductal breast carcinoma. Overall, IA significantly underestimated the conventional HER2, CEP17 counts, and HER2/CEP17 ratio; however, it collected more amplified cells in some cases below the lower limit of GH definition by manual procedure. Indicators for amplification, polysomy, and bimodality were extracted by factor analysis and allowed clustering of the tumors into amplified, nonamplified, and equivocal/polysomy categories. The bimodality indicator provided independent cell diversity characteristics for all clusters. Tumors classified as bimodal only partially coincided with the conventional GH heterogeneity category. We conclude that automated high-capacity nonselective tumor cell assay can generate evidence-based HER2 intratumor heterogeneity indicators to refine GH definitions.

Indexed as

Automation, LaboratoryIn Situ Hybridization, FluorescenceAdultBreast NeoplasmsCarcinoma, Ductal, BreastErb-b2 Receptor Tyrosine KinasesFemaleHumansERBB2 protein, humanErb-b2 Receptor Tyrosine Kinases

Identifiers

PMID28752092
PMCPMC5511668
OpenAlexW2617667181

What OpenQuestion holds

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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.