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Differentiation of malignant brain tumor types using intratumoral and peritumoral radiomic features

Tumor infiltration of central nervous system (CNS) malignant tumors may extend beyond visible contrast enhancement. This study explored tumor habitat characteristics in the intratumoral and peritumoral regions to distinguish common malignant brain tumors such as glioblastoma, primary central nervous...

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Published in:Frontiers in oncology 2022-07, Vol.12, p.848846-848846
Main Authors: Liu, Dongming, Chen, Jiu, Ge, Honglin, Hu, Xinhua, Yang, Kun, Liu, Yong, Hu, Guanjie, Luo, Bei, Yan, Zhen, Song, Kun, Xiao, Chaoyong, Zou, Yuanjie, Zhang, Wenbin, Liu, Hongyi
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Language:English
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Summary:Tumor infiltration of central nervous system (CNS) malignant tumors may extend beyond visible contrast enhancement. This study explored tumor habitat characteristics in the intratumoral and peritumoral regions to distinguish common malignant brain tumors such as glioblastoma, primary central nervous system lymphoma, and brain metastases. The preoperative MRI data of 200 patients with solitary malignant brain tumors were included from two datasets for training. Quantitative radiomic features from the intratumoral and peritumoral regions were extracted for model training. The performance of the model was evaluated using data ( n = 50) from the third clinical center. When combining the intratumoral and peritumoral features, the Adaboost model achieved the best area under the curve (AUC) of 0.91 and accuracy of 76.9% in the test cohort. Based on the optimal features and classifier, the model in the binary classification diagnosis achieves AUC of 0.98 (glioblastoma and lymphoma), 0.86 (lymphoma and metastases), and 0.70 (glioblastoma and metastases) in the test cohort, respectively. In conclusion, quantitative features from non-enhanced peritumoral regions (especially features from the 10-mm margin around the tumor) can provide additional information for the characterization of regional tumoral heterogeneity, which may offer potential value for future individualized assessment of patients with CNS tumors.
ISSN:2234-943X
2234-943X
DOI:10.3389/fonc.2022.848846