ArticleFrontiers in oncology2024
VASARI 2.0: a new updated MRI VASARI lexicon to predict grading and
Article in Frontiers in oncology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
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7 citing papers in PubMed.
- Spatial tumour characteristics as an indirect marker of metabolic dysregulation: evaluation for non-invasive IDH-genotyping of glioma using hybrid [18 F]FET-PET/MRI.European journal of nuclear medicine and molecular imaging · 2026Article
- Choroid plexus volume variation in patients with gliomas, glioneuronal and neuronal tumors: Associations with tumor characteristics.PloS one · 2026Observational
- GL-Net: A knowledge-guided Gaussian-gated and layered refinement network for 3D MRI segmentation of brain gliomas.PloS one · 2026Article
- Opportunities and challenges in application of VASARI features in neuro-oncology.Neuro-oncology practice · 2025Review
- Clinical and molecular characteristics and prognostic factors of diffuse astrocytoma, IDH-wildtype, not elsewhere classified.Journal of neuro-oncology · 2025Article
- Improving diagnostic accuracy in preoperative glioma classification: performance of knowledge-enhanced large language models compared with radiologists.NPJ precision oncology · 2025Article
- Predicting isocitrate dehydrogenase status in glioma using hierarchical attention-based deep 3D multiple instance learning.Frontiers in oncology · 2025Article
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10 authors.
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Abstract
Introduction: Precision medicine refers to managing brain tumors according to each patient's unique characteristics when it was realized that patients with the same type of tumor differ greatly in terms of survival, responsiveness to treatment, and toxicity of medication. Precision diagnostics can now be advanced through the establishment of imaging biomarkers, which necessitates quantitative image acquisition and processing. The VASARI (Visually AcceSAble Rembrandt Images) manual annotation methodology is an ideal and suitable way to determine the accurate association between genotype and imaging phenotype. Our work proposes an updated version of the VASARI score that is derived by changing the evaluation ranges of its components in an effort to increase the diagnostic accuracy of the VASARI manual annotation system and to find neuroimaging biomarkers in neuro-oncology with increasing reliability. Materials and methods: We gathered the histological grade and molecular status of 126 patients with glioma (Men/Women = 75/51; mean age: 55.30) by a retrospective analysis. Two residents and three neuroradiologists blindedly examined each patient using all 25 VASARI characteristics, after having appropriately modified the reference ranges in order to implement an innovative VASARI lexicon (VASARI 2.0). It was determined how well the observers agreed. A box plot and a bar plot were used in a statistical analysis to assess the distribution of the observations. After that, we ran a Wald test and univariate and multivariate logistic regressions. To find cutoff values that are predictive of a diagnosis, we also computed the odds ratios, confidence intervals, and evaluation matrices using receiver operating characteristic curves for each variable. Finally, we performed a Pearson correlation test to evaluate whether the variable grades and Results: An excellent Intraclass Correlation Coefficient (ICC) estimate was obtained. In this study, five features were part of the predictive model for determining glioma grade: F4, enhancement quality [area under the curve (AUC): 0.87]; F5, tumor-enhancing proportion (AUC: 0.70); F6, tumor-non-enhancing proportion (AUC: 0.89); F7, necrosis proportion (AUC: 0.79); and F17, diffusion characteristics (AUC: 0.75). Furthermore, six features were found to predict Discussion and conclusion: Glioma grade and isocitrate dehydrogenase (
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