Evidence map›Paper›PMID 41857399›Full record

ArticleAnnals of hematology2026

Development and validation of the ultrasound-based radiomics and deep learning prognostic models for diffuse large B-cell lymphoma.

Yue Yu, Siqin Liao, Hongda Su, Zhiyong Li, Meijuan Zheng, Cong Chen, Ensheng Xue, Zhenhu Lin

Abstract readValidation Study
In one paragraph

Article in Annals of hematology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

8 authors.

Yue Yu *Department of Ultrasound, Fujian Medical University Union Hospital, Fuzhou, 350001, Fujian, China.
Siqin Liao *PET Center, Fujian Medical University Union Hospital, Fuzhou, China.
Hongda SuDepartment of Ultrasound, the First Affiliated Hospital, Fujian Medical University, Fuzhou, China.
Zhiyong LiDepartment of Ultrasound, Fujian Medical University Union Hospital, Fuzhou, 350001, Fujian, China.
Meijuan ZhengDepartment of Ultrasound, Fujian Medical University Union Hospital, Fuzhou, 350001, Fujian, China.
Cong ChenDepartment of Ultrasound, Fujian Medical University Union Hospital, Fuzhou, 350001, Fujian, China.
Ensheng XueDepartment of Ultrasound, Fujian Medical University Union Hospital, Fuzhou, 350001, Fujian, China.
Zhenhu LinDepartment of Ultrasound, Fujian Medical University Union Hospital, Fuzhou, 350001, Fujian, China. 377579875@qq.com.

Funding

the Scientific Research Development Fund of Fujian Medical University 2024QH1039
6 · The paper itself

Abstract

Lymphoma includes fatal hematological malignancies, with diffuse large B-cell lymphoma (DLBCL) as the most common aggressive non-Hodgkin lymphoma subtype. Accurate early identification of high-risk DLBCL patients is key for individualized treatment and improved outcomes. This study developed and validated two ultrasound-based radiomics and deep learning prognostic models for DLBCL, and evaluated their utility in risk stratification and survival prediction. A retrospective cohort of 149 pathologically confirmed DLBCL patients was randomly split into training (n = 75) and independent test (n = 74) groups. A radiomics model and a ResNet50-based deep learning model were built on the training group, with external validation in the test group. Kaplan–Meier curves compared overall survival (OS) between risk groups. Model performance was evaluated through AUC (the primary indicator), C-index (the discrimination ability), DCA (net clinical benefit), and calibration curves (prediction-observation agreement). Both of these models were able to effectively classify patients into different risk groups (P < 0.05). The AUC values of the radiomics model in the training group were 0.819 (1 year), 0.803 (3 years), and 0.821 (5 years); in the test group, they were 0.686, 0.747, and 0.756. The AUC values of the deep learning model in the training group were 0.771, 0.782, and 0.815; in the test group, it performed better in both short-term (1 year AUC: 0.840) and long-term (3 years: 0.832; 5 years: 0.764) periods. The C index indicated that both models had high heterogeneity. DCA showed that in the training group, the imaging-based model had a higher overall net benefit, while in the test group, the deep learning model performed better. The calibration curve indicated that the radiomics model had better prediction and calibration capabilities, and might be more reliable in evaluating long-term prognosis. The ultrasound-based radiomics and ResNet50 deep learning models developed in this study demonstrate robust efficacy in predicting OS and stratifying risk in DLBCL patients. Both models are non-invasive, objective, and clinically applicable, providing valuable complementary tools for individualized prognosis evaluation and aiding clinicians in making data-driven treatment decisions for DLBCL patients.

Indexed as

Deep LearningLymphoma, Large B-Cell, DiffuseRadiomicsAdultAgedFemaleHumansMaleMiddle AgedPrognosisRetrospective StudiesUltrasonographyDiffuse large B-cell lymphomaPrognostic ModelRadiomicsResNet50Ultrasound

Identifiers

PMID41857399
PMCPMC13002698

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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.