ArticlePNAS nexus2025
AI system for diagnosing mucosa-associated lymphoid tissue lymphoma and diffuse large B cell lymphoma using ImageNet and hematoxylin and eosin-stained specimens.
Article in PNAS nexus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
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.
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.
Who cites it
3 citing papers in PubMed.
- Deep Learning Based on B-Mode and Color Doppler Ultrasound for Differentiation of Primary Thyroid Lymphoma and Hashimoto's Thyroiditis: A Retrospective Single-Center Study.Diagnostics (Basel, Switzerland) · 2026Article
- AI in Digital Pathology for Diffuse Large B-cell Lymphoma: A Systematic Review of Diagnosis and Classification.Cureus · 2025Review
- Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
AI-assisted morphological analysis using whole-slide images (WSIs) shows promise in supporting complex pathological diagnosis. However, the implementation in clinical settings is costly and demands extensive data storage. This study aimed to develop a compact, practical classification model using patch images selected by pathologists from representative disease areas under a microscope. To evaluate the limits of classification performance, we applied multiple pretraining strategies and convolutional neural networks (CNNs) specifically for the diagnosis of particularly challenging malignant lymphomas and their subtypes. The EfficientNet CNN, pretrained with ImageNet, exhibited the highest classification performance among the tested models. Our model achieved notable accuracy in a four-class classification (normal lymph node and three B cell lymphoma subtypes) using only hematoxylin and eosin-stained specimens (AUC = 0.87), comparable to results from immunohistochemical and genetic analyses. This finding suggests that the proposed model enables pathologists to independently prepare image data and easily access the algorithm and enhances diagnostic reliability while significantly reducing costs and time for additional tests, offering a practical and efficient diagnostic support tool for general medical facilities.
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Registered trials
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.