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Targeted gene expression profiling predicts meningioma outcomes and radiotherapy responses
David Raleigh1, William Chen2, Abrar Choudhury3
1University of California San Francisco.
A new gene expression biomarker improves meningioma risk stratification and predicts response to radiotherapy, outperforming current methods for better patient management.
Area of Science:
- Neuro-oncology
- Genomics
- Cancer Biomarkers
Background:
- Meningioma, the most common primary intracranial tumor, requires improved risk stratification beyond current standards.
- Postoperative radiotherapy indications for meningioma remain controversial, highlighting the need for better prognostic tools.
Approach:
- Developed and validated a 34-gene expression biomarker and risk score for predicting meningioma clinical outcomes.
- Compared the biomarker's performance against nine other classification systems in a large, multi-institutional cohort (N=1856).
Key Points:
- The gene expression biomarker significantly improved prediction of local recurrence (AUC 0.81) and overall survival (AUC 0.80) compared to existing methods.
- It identified meningiomas likely to benefit from postoperative radiotherapy, with a hazard ratio of 0.54.
- The biomarker re-classified a substantial proportion of meningiomas (up to 52.0%), suggesting refined postoperative management for nearly 30% of patients.
Conclusions:
- A targeted gene expression biomarker offers superior discrimination of meningioma outcomes.
- This biomarker accurately predicts response to postoperative radiotherapy, enabling more personalized treatment strategies.
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