# Development of a hybrid 2.5D deep learning model for glioma survival prediction using T1-weighted MRI from the CGGA database

**Authors:** Kai Jin, Caixing Sun, Liang Xia

PMC · DOI: 10.1016/j.ejro.2025.100697 · European Journal of Radiology Open · 2025-10-26

## TL;DR

A new non-invasive deep learning model using MRI scans improves survival prediction for glioma patients, combining imaging and clinical data.

## Contribution

A hybrid 2.5D deep learning model for glioma survival prediction using T1CE MRI and clinical data is developed and validated.

## Key findings

- The combined model achieved a testing C-index of 0.804, outperforming other models.
- Time-dependent AUC values ranged from 0.851 to 0.906 over 1–5 years.
- Stratified survival curves showed distinct prognostic groups with log-rank p < 0.001.

## Abstract

Current glioma survival prediction relies on invasive molecular profiling. To overcome this, a non-invasive deep learning framework using T1-weighted contrast-enhanced MRI (T1CE) was developed to predict overall survival. This framework addresses computational limitations associated with the volumetric analysis while preserving important spatial information.

We designed a hybrid 2.5D convolutional neural network to process multi-slice inputs, including the center slice and its adjacent slices, from 217 patients in the CGGA database. Transfer learning using ResNet and DenseNet architectures were employed to initialize the models. These models were subsequently fine-tuned with the Cox proportional hazards loss function. After the fine-tuning process was completed, the imaging signature was combined with clinical and molecular variables, including IDH and 1p19q status, to build an integrated model. Performance was evaluated via C-index, time-dependent AUC, and Kaplan-Meier analysis in independent training (70 %) and testing (30 %) cohorts.

The Combined model achieved superior discrimination, with a training C-index of 0.819 (95 % CI: 0.758–0.880) and a testing C-index of 0.804 (95 % CI: 0.708–0.900). It significantly outperformed the isolated Radiomic, deep learning (2D and 2.5D), and Clinical models (all p < 0.05). Moreover, time-dependent ROC analysis demonstrated consistent model performance over 1–5 years, with AUC values ranging from 0.851 to 0.906. The stratified survival curves clearly revealed distinct prognostic groups (log-rank p < 0.001).

The 2.5D multi-source framework provides a clinically feasible, non-invasive tool for preoperative survival prediction, enabling personalized therapeutic strategies for glioma patients.

## Linked entities

- **Diseases:** glioma (MONDO:0021042)

## Full-text entities

- **Genes:** IDH1 (isocitrate dehydrogenase (NADP(+)) 1) [NCBI Gene 3417] {aka HEL-216, HEL-S-26, IDCD, IDH, IDP, IDPC}
- **Diseases:** glioma (MESH:D005910)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12596209/full.md

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12596209/full.md

## References

23 references — full list in the complete paper: https://tomesphere.com/paper/PMC12596209/full.md

---
Source: https://tomesphere.com/paper/PMC12596209