Evidence map›Paper›PMID 42142114›Full record

ArticleEuropean radiology2026

Robust deep learning for incomplete MRI sequences in glioma grading and IDH mutation status prediction: a large-scale multicenter study.

Fangrong Liang, Jing Yan, Shengsheng Lai, Chaoli Zhang, Jiaxin Lin, Ruili Wei, Yuankui Wu, Jingliang Cheng, Yaou Liu, Wensheng Wang and 2 more

Abstract readMulticenter Study
PubMed Publisher
In one paragraph

Article in European radiology, 2026. 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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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

12 authors.

Fangrong Liang *Department of Radiology, School of Medicine, The Second Affiliated Hospital of South China University of Technology (Guangzhou First People's Hospital), Guangzhou, China.
Jing Yan *Department of MRI, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Shengsheng LaiSchool of Medical Equipment, Guangdong Food and Drug Vocational College, Guangzhou, China.
Chaoli ZhangDepartment of MRI, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Jiaxin LinDepartment of Radiology, School of Medicine, The Second Affiliated Hospital of South China University of Technology (Guangzhou First People's Hospital), Guangzhou, China.
Ruili WeiDepartment of Radiology, School of Medicine, The Second Affiliated Hospital of South China University of Technology (Guangzhou First People's Hospital), Guangzhou, China.
Yuankui WuDepartment of Radiology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Jingliang ChengDepartment of MRI, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Yaou LiuDepartment of Radiology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
Wensheng WangDepartment of Radiology, Guangdong Sanjiu Brain Hospital, Guangdong, China.
Xin ZhenSchool of Biomedical Engineering, Southern Medical University, Guangzhou, China. xinzhen@smu.edu.cn.
Ruimeng YangDepartment of Radiology, School of Medicine, The Second Affiliated Hospital of South China University of Technology (Guangzhou First People's Hospital), Guangzhou, China. eyruimengyang@scut.edu.cn.ORCID http://orcid.org/0000-0003-2768-9429

Funding

Guangzhou Key Laboratory of Molecular Imaging and Clinical Translational Medicine 202201020376he Guangdong Natural Science Foundation 2024A1515012100Medical Science and Technology Research Project of Guangdong Province A2024637the Excellent Youth Talent Cultivation Program of Innovation in Health Science and Technology of Henan Province YXKC2022061the Guangdong Basic and Applied Basic Research Foundation 2021A1515220060the Guangdong Natural Science Foundation 2024A1515012177the National Natural Science Foundation of China 82371908, 81971574the National Natural Science Foundation of China 82472069, 82102149the Natural Science Foundation of Henan Province for Excellent Young Scholars 252300421120the Special Training Program for Clinical Medical Scientists under the "Three 100" Initiative of Henan Province HNCMS202426
6 · The paper itself

Abstract

objectivesIncomplete MRI sequences pose a significant challenge to the reliability of multiparametric MRI (mp-MRI) radiomics models. This study aimed to develop a robust and noninvasive approach for accurate glioma grading and isocitrate dehydrogenase (IDH) mutation status prediction using incomplete MRI data. MATERIALS AND

methodsConventional MRI scans of 2170 glioma patients were retrospectively collected from five clinical institutions and a public dataset. Radiomic features extracted from each sequence, including incomplete ones, were processed using a robust incomplete sequence estimation network (RISEN). This model imputes missing features and learns latent fusion representations for glioma grading and IDH mutation status prediction. Model performance was evaluated by determining the optimal combination of mp-MRI sequences and simulating various clinical scenarios with different rates of missing data, using the area under the curve (AUC).

resultsThe optimal sequence combination of T1WI, CE-T1WI, and T2-FLAIR achieved the highest performance for glioma grading (AUC: 0.8160, 0.9136, 0.8031) and IDH prediction (AUC: 0.8657, 0.8731, 0.7682) in internal and external validation datasets with complete data. In simulated incomplete-sequence scenarios, RISEN exhibited only moderate declines for glioma grading (mean AUC: 0.7942, 0.8955, 0.7759) and IDH prediction (mean AUC: 0.8454, 0.8478, 0.7414). Comparable robustness was observed in real-world missing-sequence data (AUC: 0.8910 and 0.8854, respectively).

conclusionRISEN demonstrates robust and clinically applicable performance for glioma grading and IDH mutation prediction across multiple cohorts, even under commonly encountered incomplete mp-MRI conditions. KEY POINTS: Question Incomplete MRI sequences present a major challenge for radiomics-based glioma grading and IDH mutation status prediction in real-world clinical settings. Findings The proposed RISEN model imputes missing features using latent representations, improving model robustness and maintaining high predictive performance across various missing data scenarios. Clinical relevance RISEN offers a reliable solution for real-world glioma diagnosis when MRI sequences are incomplete, ensuring consistent clinical decision-making and personalized therapy planning across diverse imaging conditions.

Indexed as

Brain NeoplasmsDeep LearningGliomaIsocitrate DehydrogenaseMagnetic Resonance ImagingAdultFemaleHumansMaleMiddle AgedMutationNeoplasm GradingRadiomicsReproducibility of ResultsRetrospective StudiesIsocitrate DehydrogenaseGlioma gradingIncomplete sequencesIsocitrate dehydrogenaseMultiparametric magnetic resonance imagingRadiomics

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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.