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Predicting p53 Status in IDH-Mutant Gliomas Using MRI-Based Radiomic Model
Jiamin Li1,2, Zhihong Lan1, Xiao Zhang3,4,5
1Department of Radiology, Zhuhai People's Hospital, Zhuhai Hospital Affiliated With Jinan University, Zhuhai, China.
Cancer Medicine
|August 1, 2025
Summary
Radiomics analysis of contrast-enhanced T1-weighted imaging (CE-T1WI) can accurately predict p53 mutation status in isocitrate dehydrogenase-mutant (IDH-mt) gliomas noninvasively. Peritumoral edema features showed the most promise for reflecting tumor heterogeneity and predicting p53 status.
Area of Science:
- Neuro-oncology
- Medical imaging
- Radiomics
Background:
- Accurate p53 status prediction is crucial for molecular stratification of isocitrate dehydrogenase-mutant (IDH-mt) gliomas.
- Noninvasive methods for assessing p53 status in IDH-mt gliomas are challenging but clinically significant.
Purpose of the Study:
- To evaluate the diagnostic efficacy of radiomics using pre-surgery contrast-enhanced T1-weighted imaging (CE-T1WI) for predicting p53 status in IDH-mt gliomas.
- To develop and validate radiomic models and a clinical-radiomics nomogram for p53 status prediction.
Main Methods:
- Radiomic features were extracted from three volumes of interest (entire tumor, peritumoral edema, and combined) in 78 IDH-mt glioma patients.
- Machine learning algorithms were used for feature selection and model development (Rad_VOIT, Rad_VOIPE, Rad_VOIT + PE).
- A clinical-radiomics nomogram was constructed integrating age and radiomic scores, with performance assessed by ROC analysis.
Main Results:
- The peritumoral edema (VOIPE) radiomic model showed the highest predictive performance (AUC 0.811 in training, 0.810 in validation).
- A clinical-radiomics nomogram incorporating age and radiomic scores achieved excellent discrimination (AUC 0.969 in training, 0.929 in validation).
Conclusions:
- CE-T1WI-based radiomic models can noninvasively predict p53 mutation status in IDH-mt gliomas.
- Textural features of peritumoral edema may better reflect tumor heterogeneity associated with p53 status.

