Evidence map›Paper›PMID 34383240›Full record

ArticleHistochemistry and cell biology2021

How the variability between computer-assisted analysis procedures evaluating immune markers can influence patients' outcome prediction.

Marylène Lejeune, Benoît Plancoulaine, Nicolas Elie, Ramon Bosch, Laia Fontoura, Izar de Villasante, Anna Korzyńska, Andrea Gras Navarro, Esther Sauras Colón, Carlos López

Abstract read
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In one paragraph

Article in Histochemistry and cell biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. In focus in HCB.Histochemistry and cell biology · 2023
    Article
  2. Article
  3. 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

10 authors.

Marylène Lejeune *Department of Pathology, Oncological Pathology and Bioinformatics Research Group, Hospital de Tortosa Verge de la Cinta, Carrer de les Esplanetes, 14, 43500, Tortosa, Spain. mlejeune.ebre.ics@gencat.cat.ORCID http://orcid.org/0000-0001-8441-9404
Benoît Plancoulaine *Normandie University, UNICAEN, INSERM, ANTICIPE, Espl. de La Paix, 14000, Caen, France.ORCID http://orcid.org/0000-0002-4913-3184
Nicolas ElieNormandie University, UNICAEN, SFR ICORE, CMAbio3, Espl. de la Paix, 14000, Caen, France.
Ramon BoschDepartment of Pathology, Oncological Pathology and Bioinformatics Research Group, Hospital de Tortosa Verge de la Cinta, Carrer de les Esplanetes, 14, 43500, Tortosa, Spain.ORCID http://orcid.org/0000-0003-4104-5515
Laia FontouraDepartment of Pathology, Oncological Pathology and Bioinformatics Research Group, Hospital de Tortosa Verge de la Cinta, Carrer de les Esplanetes, 14, 43500, Tortosa, Spain.
Izar de VillasanteDepartment of Pathology, Oncological Pathology and Bioinformatics Research Group, Hospital de Tortosa Verge de la Cinta, Carrer de les Esplanetes, 14, 43500, Tortosa, Spain.
Anna KorzyńskaLaboratory of Processing and Analysis of Microscopic Images, Nalęcz Institute of Biocybernetics and Biomedical Engineering, Polish Academy of Sciences (IBIB PAN), ul. Ks. Trojdena 4, 02-109, Warsaw, Poland.ORCID http://orcid.org/0000-0002-6488-4832
Andrea Gras NavarroDepartment of Pathology, Oncological Pathology and Bioinformatics Research Group, Hospital de Tortosa Verge de la Cinta, Carrer de les Esplanetes, 14, 43500, Tortosa, Spain.ORCID http://orcid.org/0000-0001-6869-4529
Esther Sauras ColónDepartment of Pathology, Oncological Pathology and Bioinformatics Research Group, Hospital de Tortosa Verge de la Cinta, Carrer de les Esplanetes, 14, 43500, Tortosa, Spain.ORCID http://orcid.org/0000-0003-1649-938X
Carlos LópezDepartment of Pathology, Oncological Pathology and Bioinformatics Research Group, Hospital de Tortosa Verge de la Cinta, Carrer de les Esplanetes, 14, 43500, Tortosa, Spain.ORCID http://orcid.org/0000-0003-1248-3065

Funding

European Regional Development Fund 2903/335-41Instituto de Salud Carlos III PI11/0488Instituto de Salud Carlos III PI13/02501
6 · The paper itself

Abstract

Differences between computer-assisted image analysis (CAI) algorithms may cause discrepancies in the identification of immunohistochemically stained immune biomarkers in biopsies of breast cancer patients. These discrepancies have implications for their association with disease outcome. This study aims to compare three CAI procedures (A, B and C) to measure positive marker areas in post-neoadjuvant chemotherapy biopsies of patients with triple-negative breast cancer (TNBC) and to explore the differences in their performance in determining the potential association with relapse in these patients. A total of 3304 digital images of biopsy tissue obtained from 118 TNBC patients were stained for seven immune markers using immunohistochemistry (CD4, CD8, FOXP3, CD21, CD1a, CD83, HLA-DR) and were analyzed with procedures A, B and C. The three methods measure the positive pixel markers in the total tissue areas. The extent of agreement between paired CAI procedures, a principal component analysis (PCA) and Cox multivariate analysis was assessed. Comparisons of paired procedures showed close agreement for most of the immune markers at low concentration. The probability of differences between the paired procedures B/C and B/A was generally higher than those observed in C/A. The principal component analysis, largely based on data from CD8, CD1a and HLA-DR, identified two groups of patients with a significantly lower probability of relapse than the others. The multivariate regression models showed similarities in the factors associated with relapse for procedures A and C, as opposed to those obtained with procedure B. General agreement among the results of CAI procedures would not guarantee that the same predictive breast cancer markers were consistently identified. These results highlight the importance of developing additional strategies to improve the sensitivity of CAI procedures.

Indexed as

Image Processing, Computer-AssistedAlgorithmsBiomarkers, TumorHumansImmunohistochemistryNeoadjuvant TherapyTreatment OutcomeTriple Negative Breast NeoplasmsBiomarkers, TumorComputer-aided image analysisImmune responseImmunohistochemistryPredictive markersPrincipal component analysisRelapseTriple-negative breast cancer

Identifiers

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Registered trials

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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.