Evidence map›Paper›PMID 41992190›Full record

ArticleBMC medicine2026

Interpretable multimodal PET/CT-EHR fusion via mixture-of-experts for prognostic stratification in mantle cell lymphoma: a multicenter study.

Chong Jiang, Zitong Zhang, Zekun Jiang, Chongyang Ding, Yue Teng, Limin Gao, Ming Jiang, Linhao Qu, Rong Tian

Abstract readMulticenter Study
In one paragraph

Article in BMC medicine, 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

9 authors.

Chong JiangDepartment of Nuclear Medicine and Clinical Nuclear Medicine Research Lab, West China Hospital, Sichuan University, Chengdu, 610041, Sichuan, China.
Zitong ZhangDepartment of Nuclear Medicine, West China Hospital, Sichuan University, Chengdu, Sichuan, China.
Zekun JiangWest China Biomedical Big Data Center, West China Hospital, Sichuan University, Chengdu, China.
Chongyang DingDepartment of Nuclear Medicine, the First Affiliated Hospital of Nanjing Medical University, Jiangsu Province Hospital, Nanjing, China.
Yue TengDepartment of Nuclear Medicine, Nanjing Drum Tower Hospital, the Affiliated Hospital of Nanjing University Medical School, Nanjing, China.
Limin GaoDepartment of Pathology, West China Hospital, Sichuan University, Chengdu, China. Gaolimin80117@163.com.
Ming JiangDepartment of Oncology, West China Hospital of Sichuan University, Chengdu, China. jiangming79@wchscu.cn.
Linhao QuShanghai Medical College, Fudan University, Shanghai, China. lhqu20@fudan.edu.cn.
Rong TianDepartment of Nuclear Medicine, West China Hospital, Sichuan University, Chengdu, Sichuan, China. rongtiannuclear@126.com.

Funding

China Postdoctoral Science Foundation 2024M762244the National Natural Science Foundation of China 81971653the National Natural Science Foundation of China 82572319the PostDoctor Research Fund of West China Hospital,Sichuan University 2025HXBH087
6 · The paper itself

Abstract

backgroundMantle cell lymphoma (MCL) is a rare, biologically heterogeneous B-cell malignancy with highly variable outcomes. Existing prognostic tools are suboptimal. We developed an interpretable deep learning framework integrating baseline [

methodsIn this multicenter study, 187 treatment-naïve MCL patients were analyzed. A mixture-of-experts (MoE) fusion network integrated multimodal representations from PET/CT and EHR data. Expert modules comprising vision encoders, radiomics extractors, and a medical language model were integrated through an attention-based gating mechanism to construct multimodal radiomic signatures (R-signatures) predictive of progression-free survival (PFS) and overall survival (OS). R-signatures were validated and incorporated with clinical and metabolic factors into multiparametric models. Deep learning model interpretability was evaluated using attention visualization, expert-level contributions and pathologic correlation.

resultsR-signatures robustly discriminated relapse (AUC = 0.893 training, 0.755 validation) and death (AUC = 0.804 and 0.844), and independently predicted adverse outcomes (PFS: HR = 27.70, P < 0.001; OS: HR = 6.86, P = 0.001). Multiparametric models integrating R-signatures with total lesion glycolysis, β2-microglobulin, WBC, and Ki-67 outperformed conventional indices (C-indices: PFS 0.892 training, 0.781 validation; OS 0.877 training, 0.862 validation). Time-dependent ROC analyses consistently showed AUCs approaching or exceeding 0.800. Calibration and decision curve analyses confirmed excellent agreement and superior clinical net benefit. Attention maps localized high-weighted regions to hypermetabolic tumor areas, with higher R-signature values in blastoid and pleomorphic variants versus classical histology (P = 0.028 and P = 0.010).

conclusionsThis interpretable PET/CT-EHR fusion framework substantially improves prognostic precision in MCL, providing a noninvasive, clinically translatable tool for risk-adapted management.

Indexed as

Electronic Health RecordsLymphoma, Mantle-CellPositron Emission Tomography Computed TomographyAgedDeep LearningFemaleFluorodeoxyglucose F18HumansMaleMiddle AgedMultimodal ImagingPrognosisRadiomicsFluorodeoxyglucose F18Deep learningMantle cell lymphomaMultimodal fusionPET/CTPrognostic stratificationRadiomics

Identifiers

PMID41992190
PMCPMC13202896

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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.