Meningioma is the most common primary intracranial tumor in adults, and loss of NF2 function in meningiomas has been associated with a more aggressive biology, shorter time to recurrence and shorter overall survival. In this work, radiomics based biomarkers of NF2 copy number loss (NF2-L) have been assessed. Lower grey-level co-occurrence matrix cluster shade with wavelet high-high-low pass filter, lower original image first order minimum, and higher first order skewness with wavelet low-low-high pass filter were observed in tumors with NF2-L compared to tumors with no copy number loss. The classification accuracy of NF2 molecular subsets was 0.80±0.03 (precision=0.85±0.04, recall=0.73±0.05).
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