Evidence map›Paper›PMID 42441729›Full record

ArticlePLoS medicine2026

Self-explaining artificial intelligence for the classification of B cell non-Hodgkin lymphoma: A diagnostic decision support study.

Michael C Thrun, Jörg Hoffmann, Stefan W Krause, Peter Krawitz, Quirin Stier, Andreas Neubauer, Cornelia Brendel, Alfred Ultsch

Abstract read
In one paragraph

Article in PLoS medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

8 authors.

Michael C ThrunMathematics and Computer Science, Philipps University Marburg, Marburg, Germany.ORCID https://orcid.org/0000-0001-9542-5543
Jörg HoffmannDepartment of Hematology, Oncology and Immunology, Philipps University Marburg, University Hospital Giessen and Marburg, Marburg, Germany.
Stefan W KrauseDepartment of Medicine 5, Universitätsklinikum Erlangen, Erlangen, Germany.ORCID https://orcid.org/0000-0002-5259-4651
Peter KrawitzInstitute for Genomic Statistics and Bioinformatics, University Bonn, Bonn, Germany.ORCID https://orcid.org/0000-0002-3194-8625
Quirin StierMathematics and Computer Science, Philipps University Marburg, Marburg, Germany.
Andreas NeubauerDepartment of Hematology, Oncology and Immunology, Philipps University Marburg, University Hospital Giessen and Marburg, Marburg, Germany.
Cornelia BrendelDepartment of Hematology, Oncology and Immunology, Philipps University Marburg, University Hospital Giessen and Marburg, Marburg, Germany.ORCID https://orcid.org/0000-0003-1612-9557
Alfred UltschMathematics and Computer Science, Philipps University Marburg, Marburg, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMultiparameter flow cytometry is a cornerstone of B cell non-Hodgkin lymphoma (B-NHL) diagnostics, but interpretation requires substantial expertise and is complicated by high-dimensional data, variable sample quality, limited data for rare entities, and evolving clinical classification systems. Current artificial intelligence approaches often require large training datasets and provide limited insight into the rationale behind individual diagnostic decisions. METHODS AND

findingsWe developed FlowXAI, a self-explaining artificial intelligence system designed to support B-NHL classification while explicitly reporting case-level diagnostic trustworthiness. FlowXAI combines unsupervised structural analysis with a clinically motivated, multi-level diagnostic framework reflecting routine diagnostic priorities. An unsupervised Tile Mining (TM) procedure performs pre-diagnostic sample-quality assessment by identifying structurally atypical samples. TM is applied to filter training data, enabling substantial reduction of training requirements while preserving unbiased evaluation on independent test samples. FlowXAI was evaluated using repeated cross-validation on 19,493 peripheral blood samples and further assessed on an independent external benchmark dataset generated at a separate diagnostic center using a different antibody panel. Across diagnostic levels, FlowXAI achieved performance comparable to a deep learning-based system despite requiring approximately two orders of magnitude fewer training samples. When predictions were classified as confident by the system's internal self-assessment, diagnostic performance exceeded that of the neural network baseline. Unsupervised structural analysis demonstrated clear separation between normal controls and selected lymphoma entities such as chronic lymphocytic leukemia-like lymphomas and hairy cell leukemia, while other entities were not clearly separable using the antibody panels studied.

conclusionsFlowXAI provides accurate, data-efficient, and transparent support for B-NHL immunophenotyping from nonstandardized flow cytometry data. By combining interpretable decision logic with explicit self-assessment, FlowXAI offers a clinically meaningful framework for diagnostic support and training, particularly in settings with limited expert availability or rare lymphoma subtypes. The main limitation is the retrospective evaluation using specific antibody panels, and FlowXAI requires prospective validation as a decision-support tool within integrated diagnostic workflows.

Indexed as

Artificial IntelligenceDecision Support Systems, ClinicalDecision Support TechniquesLymphoma, B-CellClassification AlgorithmsFlow CytometryHumans

Identifiers

PMID42441729
PMCPMC13421771

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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.