4.6 Article

Extensive peritumoral edema and brain-to-tumor interface MRI features enable prediction of brain invasion in meningioma: development and validation

Journal

NEURO-ONCOLOGY
Volume 23, Issue 2, Pages 324-333

Publisher

OXFORD UNIV PRESS INC
DOI: 10.1093/neuonc/noaa190

Keywords

meningioma; brain invasion; MRI; radiomics; machine learning

Funding

  1. National Research Foundation of Korea (NRF) - Ministry of Education [NRF-2020R1A2B5B01001707, NRF-2020R1A2C4001748]

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An imaging-based model combining interface radiomics and peritumoral edema can help predict brain invasion by meningioma and improve diagnostic performance over known clinical and imaging parameters.
Background. Brain invasion by meningioma is a stand-alone criterion for tumor atypia in the 2016 World Health Organization classification, but no imaging parameter has yet been shown to be sufficient for predicting it. The aim of this study was to develop and validate an MRI-based radiomics model from the brain-to-tumor interface to predict brain invasion by meningioma. Methods. Preoperative T2-weighted and contrast-enhanced T1-weighted imaging data were obtained from 454 patients (88 patients with brain invasion) between 2012 and 2017. Feature selection was performed from 3222 radiomics features obtained in the 1 cm thickness tumor-to-brain interface region using least absolute shrinkage and selection operator. Peritumoral edema volume, age, sex, and selected radiomics features were used to construct a random forest classifier-based diagnostic model. The performance was evaluated using the areas under the curves (AUCs) of the receiver operating characteristic in an independent cohort of 150 patients (29 patients with brain invasion) between 2018 and 2019. Results. Volume of peritumoral edema was an independent predictor of brain invasion (P < 0.001). The top 6 interface radiomics features plus the volume of peritumoral edema were selected for model construction. The combined model showed the highest performance for prediction of brain invasion in the training (AUC 0.97; 95% CI: 0.95-0.98) and validation sets (AUC 0.91; 95% CI: 0.84-0.98), and improved diagnostic performance over volume of peritumoral edema only (AUC 0.76; 95% CI: 0.66-0.86). Conclusion. An imaging-based model combining interface radiomics and peritumoral edema can help to predict brain invasion by meningioma and improve the diagnostic performance of known clinical and imaging parameters.

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