Evidence map›Paper›PMID 42310216›Full record

ArticleEuropean journal of nuclear medicine and molecular imaging2026

Deep integration of clinical metadata with [

Jucheng Zhang, Xiaohui Zhang, Jing Wang, Han Hao, Daoyan Hu, Kangjun Hu, Xuena Li, Yaming Li, Guanghui Liu, Rong Tian and 7 more

Abstract readMulticenter Study
PubMed Publisher
In one paragraph

Article in European journal of nuclear medicine and molecular imaging, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

17 authors.

Jucheng Zhang *Department of Clinical Engineering, The Second Affiliated Hospital of Zhejiang University School of Medicine, Hangzhou, Zhejiang, 310009, China.
Xiaohui Zhang *Institute of Nuclear Medicine and Molecular Imaging of Zhejiang University, Hangzhou, Zhejiang, 310009, China.
Jing Wang *Institute of Nuclear Medicine and Molecular Imaging of Zhejiang University, Hangzhou, Zhejiang, 310009, China.
Han HaoThe Polytechnic Institute, Zhejiang University, Hangzhou, Zhejiang, 310015, China.
Daoyan HuCollege of Biomedical Engineering & Instrument Science, Zhejiang University, Hangzhou, Zhejiang, 310027, China.
Kangjun HuCollege of Biomedical Engineering & Instrument Science, Zhejiang University, Hangzhou, Zhejiang, 310027, China.
Xuena LiDepartment of Nuclear Medicine, The First Hospital of China Medical University, 155 Nanjing St, Shenyang, Liaoning, 110001, China.
Yaming LiDepartment of Nuclear Medicine, The First Hospital of China Medical University, 155 Nanjing St, Shenyang, Liaoning, 110001, China.
Guanghui LiuDepartment of Nuclear Medicine, The First Hospital of China Medical University, 155 Nanjing St, Shenyang, Liaoning, 110001, China.
Rong TianDepartment of Nuclear Medicine, West China Hospital, Sichuan University, Chengdu, Sichuan, 610041, China.
Weiming WuDepartment of Nuclear Medicine, West China Hospital, Sichuan University, Chengdu, Sichuan, 610041, China.
Xiaofen MaDepartment of Nuclear Medicine, The Affiliated Guangdong Second Provincial General Hospital of Jinan University, Guangzhou, Guangdong, 510317, China.
Yile HuangDepartment of Nuclear Medicine, The Second School of Clinical Medicine, Southern Medical University, Guangzhou, Guangdong, 510317, China.
Chentao JinInstitute of Nuclear Medicine and Molecular Imaging of Zhejiang University, Hangzhou, Zhejiang, 310009, China.
Yan ZhongInstitute of Nuclear Medicine and Molecular Imaging of Zhejiang University, Hangzhou, Zhejiang, 310009, China. yanzhong@zju.edu.cn.
Mei TianHuman Phenome Institute, Fudan University, Shanghai, 201203, China. tianmei@fudan.edu.cn.
Hong ZhangInstitute of Nuclear Medicine and Molecular Imaging of Zhejiang University, Hangzhou, Zhejiang, 310009, China. hzhang21@zju.edu.cn.ORCID 0000-0002-4084-5150

Funding

Key Technologies Research and Development Program 2021YFA1101700National Natural Science Foundation of China 82361148130National Natural Science Foundation of China 82372025National Natural Science Foundation of China 82394433
6 · The paper itself

Abstract

purposeTo develop and validate a multimodal deep learning framework that integrates clinical metadata with [

methodsA multi-center surgical NSCLC cohort (n = 780) was partitioned into a development set (n = 675) and an independent external test set (n = 105). The framework first utilized a 3D Transformer for bounding-box-based tumor localization. Subsequently, a multi-task network employed Feature-wise Linear Modulation (FiLM) to dynamically inject clinical metadata into the visual backbone.

resultsFor histological subtyping of adenocarcinoma versus squamous cell carcinoma, in the validation cohort, the proposed multimodal framework achieved the highest area under the receiver operating characteristic curve (AUC) of 0.894 (95% CI: 0.813-0.959), significantly outperforming the conventional radiomics baseline (AUC = 0.796, DeLong test P = 0.017) and the clinical-only baseline (AUC = 0.759, P = 0.004). On the internal test set, the multimodal model maintained an AUC of 0.832 (95% CI: 0.744-0.906), outperforming competing models numerically, though differences did not reach statistical significance (all P > 0.11). On the independent external test cohort, the multimodal framework demonstrated superior cross-center stability, maintaining an AUC of 0.787 (95% CI: 0.687-0.876). On the external cohort, the between-model AUC differences did not reach statistical significance against the clinical-only model (AUC of 0.740, P = 0.480) or the image-only model (AUC of 0.685, P = 0.082). Nevertheless, the multimodal framework achieved the highest F1-score and yielded the most optimal net clinical benefit across a wide range of threshold probabilities in decision curve analysis. For the intrinsically challenging auxiliary staging task, the unguided image-only network exhibited severe vulnerability, however, the FiLM-based multimodal mechanism effectively enhanced diagnostic capacity by employing systemic clinical priors, improving the AUC to 0.656.

conclusionCombining 3D detection with an early clinico-biological fusion strategy effectively enhances NSCLC characterization on [

Indexed as

Carcinoma, Non-Small-Cell LungDeep LearningFluorodeoxyglucose F18Image Processing, Computer-AssistedLung NeoplasmsPositron Emission Tomography Computed TomographyFemaleHumansMaleRadiomicsFluorodeoxyglucose F18[18F]FDG PET/CTDeep learningHistologic subtypeNSCLCRadiomics

Identifiers

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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 Socratic graph.