Evidence map›Paper›PMID 36717673›Full record

ArticleBritish journal of cancer2023

Predicting the HER2 status in oesophageal cancer from tissue microarrays using convolutional neural networks.

Juan I Pisula, Rabi R Datta, Leandra Börner Valdez, Jan-Robert Avemarg, Jin-On Jung, Patrick Plum, Heike Löser, Philipp Lohneis, Monique Meuschke, Daniel Pinto Dos Santos and 7 more

Open access · hybridFull text 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 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.3field-weighted citation impact, top 10% 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

10 citing papers in PubMed, 13 citations in OpenAlex.

  1. Review
  2. Esophageal cancer: from pathogenesis to precision therapies.Signal transduction and targeted therapy · 2026
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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

17 authors at 3 institutions in 1 country.

Juan I PisulaData science of Bioimages Lab, Faculty of Medicine and University Hospital Cologne, Center for Molecular Medicine Cologne (CMMC), University of Cologne, 50931, Cologne, Germany.
Rabi R DattaDepartment of General, Visceral, Cancer and Transplantation Surgery, University of Cologne, 50937, Cologne, Germany.
Leandra Börner ValdezDepartment of General, Visceral, Cancer and Transplantation Surgery, University of Cologne, 50937, Cologne, Germany.
Jan-Robert AvemargFaculty of Mathematics and Computer Science, Friedrich Schiller University Jena, 07743, Jena, Germany.
Jin-On JungDepartment of General, Visceral, Cancer and Transplantation Surgery, University of Cologne, 50937, Cologne, Germany.
Patrick PlumDepartment of General, Visceral, Cancer and Transplantation Surgery, University of Cologne, 50937, Cologne, Germany.
Heike LöserInstitute of Pathology, University of Cologne, 50937, Cologne, Germany.
Philipp LohneisInstitute of Pathology, University of Cologne, 50937, Cologne, Germany.
Monique MeuschkeFaculty of Mathematics and Computer Science, Friedrich Schiller University Jena, 07743, Jena, Germany.
Daniel Pinto Dos SantosDepartment of Radiology, University of Cologne, 50937, Cologne, Germany.
Florian GebauerDepartment of General, Visceral, Cancer and Transplantation Surgery, University of Cologne, 50937, Cologne, Germany.
Alexander QuaasInstitute of Pathology, University of Cologne, 50937, Cologne, Germany.
Axel WalchResearch Unit Analytical Pathology, Helmholtz Zentrum München, 85764, Neuherberg, Germany.
Christiane J BrunsDepartment of General, Visceral, Cancer and Transplantation Surgery, University of Cologne, 50937, Cologne, Germany.
Kai LawonnFaculty of Mathematics and Computer Science, Friedrich Schiller University Jena, 07743, Jena, Germany.
Felix C Popp *Department of General, Visceral, Cancer and Transplantation Surgery, University of Cologne, 50937, Cologne, Germany.
Katarzyna Bozek *Data science of Bioimages Lab, Faculty of Medicine and University Hospital Cologne, Center for Molecular Medicine Cologne (CMMC), University of Cologne, 50931, Cologne, Germany. k.bozek@uni-koeln.de.ORCID 0000-0002-0917-6876
University of Cologne · DEFriedrich Schiller University Jena · DEHelmholtz Zentrum München · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundFast and accurate diagnostics are key for personalised medicine. Particularly in cancer, precise diagnosis is a prerequisite for targeted therapies, which can prolong lives. In this work, we focus on the automatic identification of gastroesophageal adenocarcinoma (GEA) patients that qualify for a personalised therapy targeting epidermal growth factor receptor 2 (HER2). We present a deep-learning method for scoring microscopy images of GEA for the presence of HER2 overexpression.

methodsOur method is based on convolutional neural networks (CNNs) trained on a rich dataset of 1602 patient samples and tested on an independent set of 307 patient samples. We additionally verified the CNN's generalisation capabilities with an independent dataset with 653 samples from a separate clinical centre. We incorporated an attention mechanism in the network architecture to identify the tissue regions, which are important for the prediction outcome. Our solution allows for direct automated detection of HER2 in immunohistochemistry-stained tissue slides without the need for manual assessment and additional costly in situ hybridisation (ISH) tests.

resultsWe show accuracy of 0.94, precision of 0.97, and recall of 0.95. Importantly, our approach offers accurate predictions in cases that pathologists cannot resolve and that require additional ISH testing. We confirmed our findings in an independent dataset collected in a different clinical centre. The attention-based CNN exploits morphological information in microscopy images and is superior to a predictive model based on the staining intensity only.

conclusionsWe demonstrate that our approach not only automates an important diagnostic process for GEA patients but also paves the way for the discovery of new morphological features that were previously unknown for GEA pathology.

Indexed as

AdenocarcinomaEsophageal NeoplasmsErbB ReceptorsHumansIn Situ HybridizationNeural Networks, ComputerErbB Receptors

Identifiers

PMID36717673
PMCPMC10050393
OpenAlexW4318590625

What OpenQuestion holds

Textfull text, public
LicenceCC BY
measurements read9
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.