Evidence map›Paper›PMID 40927175›Full record

ArticleFrontiers in veterinary science2025

Deep-learning based morphological segmentation of canine diffuse large B-cell lymphoma.

Kenneth Ancheta, Androniki Psifidi, Andrew D Yale, Sophie Le Calvez, Jonathan Williams

Abstract read
In one paragraph

Article in Frontiers in veterinary science, 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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0citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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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

5 authors.

Kenneth AnchetaPathobiology and Population Science, Royal Veterinary College, Hatfield, United Kingdom.
Androniki PsifidiClinical Science and Services, Royal Veterinary College, Hatfield, United Kingdom.
Andrew D YaleClinical Science and Services, Royal Veterinary College, Hatfield, United Kingdom.
Sophie Le CalvezIDEXX Laboratories Ltd., Wetherby, United Kingdom.
Jonathan WilliamsPathobiology and Population Science, Royal Veterinary College, Hatfield, United Kingdom.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Diffuse large B-cell lymphoma is the most common type of non-Hodgkin lymphoma (NHL) in humans, accounting for about 30-40% of NHL cases worldwide. Canine diffuse large B-cell lymphoma (cDLBCL) is the most common lymphoma subtype in dogs and demonstrates an aggressive biologic behaviour. For tissue biopsies, current confirmatory diagnostic approaches for enlarged lymph nodes rely on expert histopathological assessment, which is time-consuming and requires specialist expertise. Therefore, there is an urgent need to develop tools to support and improve veterinary diagnostic workflows. Advances in molecular and computational approaches have opened new avenues for morphological analysis. This study explores the use of convolutional neural networks (CNNs) to differentiate cDLBCL from non-neoplastic lymph nodes, specifically reactive lymphoid hyperplasia (RLH). Whole slide images (WSIs) of haematoxylin-eosin stained lymph node slides were digitised at 20 × magnification and pre-processed using a modified Aachen protocol. Extracted images were split at the patient level into training (60%), validation (30%), and testing (10%) datasets. Here, we introduce HawksheadNet, a novel lightweight CNN architecture for cancer image classification and highlight the critical role of stain normalisation in CNN training. Once fine-tuned, HawksheadNet demonstrated strong generalisation performance in differentiating cDLBCL from RLH, achieving an area under the receiver operating characteristic (AUROC) of up to 0.9691 using fine-tuned parameters on StainNet-normalised images, outperforming pre-trained CNNs such as EfficientNet (up to 0.9492), Inception (up to 0.9311), and MobileNet (up to 0.9498). Additionally, WSI segmentation was achieved by overlaying the tile-wise predictions onto the original slide, providing a visual representation of the diagnosis that closely aligned with pathologist interpretation. Overall, this study highlights the potential of CNNs in cancer image analysis, offering promising advancements for clinical pathology workflows, patient care, and prognostication.

Indexed as

artificial intelligencecaninedeep learningdigital pathologylymphoma

Identifiers

PMID40927175
PMCPMC12415696

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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.