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Objectives: We aimed to evaluate the diagnostic performance of deep learning (DL)-based radiomics models for the noninvasive prediction of isocitrate dehydrogenase (IDH) mutation and 1p/19q co-deletion status in glioma patients using MRI sequences, and to identify methodological factors influencing accuracy and generalizability.
Materials And Methods: Following PRISMA guidelines, we systematically searched major databases (PubMed, Scopus, Embase, Web of Science, and Google Scholar) up to March 2025, screening studies that utilized DL to predict IDH and 1p/19q co-deletion status from MRI data. We assessed study quality and risk of bias using the Radiomics Quality Score and the QUADAS-2 tool. Our meta-analysis employed a bivariate model to compute pooled sensitivity and specificity, and meta-regression to assess interstudy heterogeneity.
Results: Among the 1517 unique publications, 104 were included in the qualitative synthesis, and 72 underwent meta-analysis. Pooled estimates for IDH prediction in test cohorts yielded a sensitivity of 0.80 (95% CI: 0.77-0.83) and specificity of 0.85 (95% CI: 0.81-0.87). For 1p/19q co-deletion, sensitivity was 0.75 (95% CI: 0.65-0.82) and specificity was 0.82 (95% CI: 0.75-0.88). Meta-regression identified the tumor segmentation method and the extent of DL integration into the radiomics pipeline as significant contributors to interstudy variability.
Conclusion: Although DL models demonstrate strong potential for noninvasive molecular classification of gliomas, clinical translation requires several critical steps: harmonization of multi-center MRI data using techniques such as histogram matching and DL-based style transfer; adoption of standardized and automated segmentation protocols; extensive multi-center external validation; and prospective clinical validation.
Key Points: Question Can DL based radiomics using routine MRI noninvasively predict IDH mutation and 1p/19q co-deletion status in gliomas, and what factors affect diagnostic accuracy? Findings Meta-analysis showed 80% sensitivity and 85% specificity for predicting IDH mutation, and 75% sensitivity and 82% specificity for 1p/19q co-deletion status. Clinical relevance MRI-based DL models demonstrate clinically useful accuracy for noninvasive glioma molecular classification, but data harmonization, standardized automated segmentation, and rigorous multi-center external validation are essential for clinical adoption.
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http://dx.doi.org/10.1007/s00330-025-11898-2 | DOI Listing |
Sci Rep
September 2025
Department of Neurosurgery, Shenzhen Second People's Hospital, The First Affiliated Hospital of Shenzhen University Health Science Center, Shenzhen, 518035, P.R. China.
Glioblastoma multiforme (GBM) is a lethal brain tumor with limited therapies. NUF2, a kinetochore protein involved in cell cycle regulation, shows oncogenic potential in various cancers; however, its role in GBM pathogenesis remains unclear. In this study, we investigated NUF2's function and mechanisms in GBM and developed an MRI-based machine learning model to predict its expression non-invasively, and evaluated its potential as a therapeutic target and prognostic biomarker.
View Article and Find Full Text PDFFree Radic Biol Med
August 2025
Department of Biotherapy, Cancer Center and State Key Laboratory of Biotherapy, West China Hospital, Sichuan University, Chengdu, 610041, China. Electronic address:
Gliomas are highly aggressive and heterogeneous brain tumors with poor clinical outcomes, necessitating an urgent need for novel prognostic biomarkers and therapeutic targets. Redox regulation, which balances reactive oxygen species (ROS) generation with antioxidant defense mechanisms, has emerged as a crucial adaptive mechanism supporting glioma progression. However, the precise roles and clinical implications of redox-associated genes in glioma remain poorly defined.
View Article and Find Full Text PDFEur Radiol
August 2025
Centre for Health Informatics, Australian Institute of Health Innovation, Macquarie University, Sydney, NSW, Australia.
Objectives: We aimed to evaluate the diagnostic performance of deep learning (DL)-based radiomics models for the noninvasive prediction of isocitrate dehydrogenase (IDH) mutation and 1p/19q co-deletion status in glioma patients using MRI sequences, and to identify methodological factors influencing accuracy and generalizability.
Materials And Methods: Following PRISMA guidelines, we systematically searched major databases (PubMed, Scopus, Embase, Web of Science, and Google Scholar) up to March 2025, screening studies that utilized DL to predict IDH and 1p/19q co-deletion status from MRI data. We assessed study quality and risk of bias using the Radiomics Quality Score and the QUADAS-2 tool.
Front Oncol
July 2025
Department of Magnetic Resonance Imaging, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Background And Purpose: In the 2021 WHO Classification, the importance of molecular pathology in glioma diagnosis has been emphasized, particularly the status of isocitrate dehydrogenase (IDH) mutation and 1p/19q co-deletion. Advanced magnetic resonance diffusion-weighted imaging (DWI) including mono-exponential (Mono), intravoxel incoherent motion (IVIM), stretched exponential model (SEM) techniques are beneficial for non-invasive prediction of these molecular markers. The continuous-time random walk (CTRW) model mitigates the empirical nature of the SEM and has shown promising results in grading gliomas.
View Article and Find Full Text PDFQuant Imaging Med Surg
August 2025
Department of Radiology, the First Hospital of China Medical University, Shenyang, China.
Background: Given the limitations of conventional imaging in accurately grading gliomas, predicting molecular subtypes, and assessing tumor proliferation and angiogenesis, there is a growing need for advanced quantitative magnetic resonance imaging (MRI) biomarkers. This study aimed to compare the diagnostic performance of histogram features of dynamic contrast enhanced (DCE) and dynamic susceptibility contrast (DSC) imaging in predicting glioma grade and genotyping, as well as to explore the association between DCE and DSC with Ki-67 and microvascular density (MVD).
Methods: Forty-six patients with gliomas were enrolled prospectively.