# Diagnostic Utility of Intratumoral Susceptibility Signals in Adult Diffuse Gliomas: Tumor Grade Prediction and Correlation with Molecular Markers Within the WHO CNS5 (2021) Classification

**Authors:** José Ignacio Tudela Martínez, Victoria Vázquez Sáez, Guillermo Carbonell, Héctor Rodrigo Lara, Florentina Guzmán-Aroca, Juan de Dios Berna Mestre

PMC · DOI: 10.3390/jcm14114004 · Journal of Clinical Medicine · 2025-06-05

## TL;DR

This study shows that intratumoral susceptibility signals (ITSS) can help predict the grade of adult diffuse gliomas and correlate with molecular markers, improving non-invasive diagnosis.

## Contribution

The study introduces semiquantitative ITSS grading as a novel imaging biomarker for glioma grading and molecular classification under WHO CNS5.

## Key findings

- Higher ITSS grades correlate with aggressive features like necrosis and CDKN2A/B deletions in glioblastomas.
- ITSS grades 0–1 are associated with IDH mutations and 1p/19q co-deletions in lower-grade gliomas.
- Combining ITSS with rCBV and tumor volume improves diagnostic accuracy for glioma grading.

## Abstract

Background/Objectives: This study evaluates intratumoral susceptibility signals (ITSS) as imaging markers for glioma grade prediction and their association with molecular and histopathologic features, in the context of the fifth edition of the World Health Organization Classification of Tumors of the Central Nervous System (WHO CNS5). Methods: We retrospectively analyzed patients with adult diffuse gliomas who underwent pretreatment magnetic resonance imaging. ITSS were semiquantitatively graded by two radiologists: grade 0 (no signal), grade 1 (1–5), grade 2 (6–10), and grade 3 (≥11). Relative cerebral blood volume (rCBV) and tumor volume were also obtained. Histopathologic features included tumor grade, Ki-67, mitotic count, necrosis, microvascular proliferation, and molecular alterations (isocitrate dehydrogenase [IDH], 1p/19q, cyclin-dependent kinase inhibitors 2A and 2B [CDKN2A/B], and p53). Regression models predicted tumor grade (low: 1–2, high: 3–4) using ITSS, tumor volume, and rCBV. ROC curves and diagnostic performance metrics were analyzed. Results: 99 patients were included. ITSS grading correlated with rCBV, tumor volume, mitotic count, Ki-67, and tumor grade (p < 0.001). ITSS grades 0–1 were associated with oligodendrogliomas and astrocytomas (p < 0.001), IDH mutations (p < 0.001), and 1p/19q co-deletions (p = 0.01). ITSS grades 2–3 were linked to glioblastomas (p < 0.001), necrosis (p < 0.001), microvascular proliferation (p < 0.001), and CDKN2A/B homozygous deletions (p = 0.02). Models combining ITSS with rCBV and volume showed AUC of 0.94 and 0.96 (p < 0.001), outperforming univariate models. Conclusions: Semiquantitative ITSS grading correlates with key histopathologic and molecular glioma features. Combined with perfusion and volumetric parameters, ITSS enhance non-invasive glioma grading, in alignment with WHO CNS5.

## Linked entities

- **Genes:** IDH1 (isocitrate dehydrogenase (NADP(+)) 1) [NCBI Gene 3417], cdkn2a/b (cyclin-dependent kinase inhibitor 2A/B (p15, inhibits CDK4)) [NCBI Gene 100329528], TP53 (tumor protein p53) [NCBI Gene 7157]
- **Diseases:** glioma (MONDO:0021042), oligodendroglioma (MONDO:0002540), astrocytoma (MONDO:0019781), glioblastoma (MONDO:0018177)

## Full-text entities

- **Genes:** TP53 (tumor protein p53) [NCBI Gene 7157] {aka BCC7, BMFS5, LFS1, P53, TRP53}, IDH1 (isocitrate dehydrogenase (NADP(+)) 1) [NCBI Gene 3417] {aka HEL-216, HEL-S-26, IDCD, IDH, IDP, IDPC}
- **Diseases:** glioblastomas (MESH:D005909), Tumors of the Central Nervous System (MESH:D016543), necrosis (MESH:D009336), glioma (MESH:D005910), oligodendrogliomas (MESH:D009837), Tumor (MESH:D009369), astrocytomas (MESH:D001254), Adult Diffuse Gliomas (MESH:D020339)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12156373/full.md

## References

31 references — full list in the complete paper: https://tomesphere.com/paper/PMC12156373/full.md

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Source: https://tomesphere.com/paper/PMC12156373