Evidence map›Paper›PMID 41168756›Full record

ArticleBMC medical imaging2025

Non-Hodgkin's lymphoma classification using 3D radiomics machine learning models for precision imaging in oncology.

Christoph G Lisson, Michael Götz, Daniel Wolf, Sabitha Manoj, Luisa Gallee, Stefan A Schmidt, Eugen Tausch, Christof Schneider, Stephan Stilgenbauer, Ambros J Beer and 3 more

Abstract read
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Article in BMC medical imaging, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

13 authors.

Christoph G Lisson *Department of Diagnostic and Interventional Radiology, University Hospital Ulm, Albert-Einstein-Allee 23, 89081, Ulm, Germany.
Michael Götz *Department of Diagnostic and Interventional Radiology, University Hospital Ulm, Albert-Einstein-Allee 23, 89081, Ulm, Germany.
Daniel WolfDepartment of Diagnostic and Interventional Radiology, University Hospital Ulm, Albert-Einstein-Allee 23, 89081, Ulm, Germany.
Sabitha ManojDepartment of Diagnostic and Interventional Radiology, University Hospital Ulm, Albert-Einstein-Allee 23, 89081, Ulm, Germany.
Luisa GalleeDepartment of Diagnostic and Interventional Radiology, University Hospital Ulm, Albert-Einstein-Allee 23, 89081, Ulm, Germany.
Stefan A SchmidtDepartment of Diagnostic and Interventional Radiology, University Hospital Ulm, Albert-Einstein-Allee 23, 89081, Ulm, Germany.
Eugen TauschDepartment of Internal Medicine III, University Hospital Ulm, Ulm, Germany.
Christof SchneiderDepartment of Internal Medicine III, University Hospital Ulm, Ulm, Germany.
Stephan StilgenbauerDepartment of Internal Medicine III, University Hospital Ulm, Ulm, Germany.
Ambros J BeerCenter for Translational Imaging "From Molecule to Man" (MoMan), Department of Internal Medicine II, University Hospital Ulm, Ulm, Germany.
Meinrad BeerDepartment of Diagnostic and Interventional Radiology, University Hospital Ulm, Albert-Einstein-Allee 23, 89081, Ulm, Germany.
Nico SollmannDepartment of Diagnostic and Interventional Radiology, University Hospital Ulm, Albert-Einstein-Allee 23, 89081, Ulm, Germany.
Catharina S LissonDepartment of Diagnostic and Interventional Radiology, University Hospital Ulm, Albert-Einstein-Allee 23, 89081, Ulm, Germany. catharina.lisson@uni-ulm.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTo apply quantitative imaging analysis for noninvasive classification of the most frequent subtypes of Non-Hodgkin Lymphoma (NHL) as a basis for a clinical imaging genomic model to support therapeutic monitoring and clinical decision making. MATERIALS AND

methodsIn this single-center study, 201 treatment-naïve patients with biopsy-proven NHL (50 diffuse large B-cell lymphoma [DLBCL], 51 mantle cell lymphoma [MCL], 49 follicular lymphoma [FL], and 51 chronic lymphocytic leukemia [CLL]) and 39 treatment-naïve non-small cell lung cancer patients with positron emission tomography (PET)/computed tomography (CT)-confirmed healthy axillary lymph nodes (LNs) were retrospectively analyzed. Three-dimensional (3D) segmentation and radiomic analysis of pathologically enlarged nodes (n = 1,628) were performed on contrast-enhanced CT scans, including healthy LNs as references. Feature selection was performed using a random forest (RF) classifier. Multiclass Classifier was performed using a Light Gradient Boosting Machine (LGBM) classifier for lymphoma subtype classification.

resultsPerformance to classify lymphoma from non-lymphoma and lymphoma subtypes was as follows: lymphoma vs. non-lymphoma: area under the curve (AUC) = 0.999; MCL vs. other NHL: AUC = 0.997; DLBCL vs. other NHL: AUC = 0.971; CLL vs. other NHL: AUC = 0.956; FL vs. other NHL: AUC = 0.892.

conclusionRadiomics combined with multiclass machine learning enables highly accurate, non-invasive differentiation of the major NHL subtypes on routine contrast-enhanced CT. By reliably separating indolent from aggressive phenotypes, this approach lays the groundwork for imaging-genomic models that could streamline biopsy guidance, enhance therapeutic monitoring, and advance precision oncology in lymphoma care.Conducted as a single-centre, retrospective proof-of-concept with internal patient-level cross-validation, these results are promising and form the basis for a prospective multicentre study to confirm generalisability and clinical utility. CLINICAL RELEVANCE STATEMENT: Accurate lymphoma classification is essential for predicting clinical behavior and guiding treatment. Imaging aids in disease staging, with quantitative analysis showing promise in predicting pathology and outcome. We explored machine learning on imaging features for lymphoma classification, thus enhancing clinical decisions.

Indexed as

Imaging, Three-DimensionalLymphoma, Non-HodgkinMachine LearningPositron Emission Tomography Computed TomographyAdultAgedAged, 80 and overFemaleHumansLymph NodesMaleMiddle AgedRadiomicsRetrospective StudiesImaging biomarkers.Lymph nodesMachine learningNon-Hodgkin lymphomaPrecision oncologyRadiomics

Identifiers

PMID41168756
PMCPMC12577418

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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.