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Radiomic features from multiparametric magnetic resonance imaging predict molecular subgroups of pediatric low-grade gliomas

BACKGROUND: We aimed to develop machine learning models for prediction of molecular subgroups (low-risk group and intermediate/high-risk group) and molecular marker (KIAA1549-BRAF fusion) of pediatric low-grade gliomas (PLGGs) based on radiomic features extracted from multiparametric MRI. METHODS: 6...

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Detalles Bibliográficos
Autores principales: Liu, Zhen, Hong, Xuanke, Wang, Linglong, Ma, Zeyu, Guan, Fangzhan, Wang, Weiwei, Qiu, Yuning, Zhang, Xueping, Duan, Wenchao, Wang, Minkai, Sun, Chen, Zhao, Yuanshen, Duan, Jingxian, Sun, Qiuchang, Liu, Lin, Ding, Lei, Ji, Yuchen, Yan, Dongming, Liu, Xianzhi, Cheng, Jingliang, Zhang, Zhenyu, Li, Zhi-Cheng, Yan, Jing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10496393/
https://www.ncbi.nlm.nih.gov/pubmed/37697238
http://dx.doi.org/10.1186/s12885-023-11338-8
Descripción
Sumario:BACKGROUND: We aimed to develop machine learning models for prediction of molecular subgroups (low-risk group and intermediate/high-risk group) and molecular marker (KIAA1549-BRAF fusion) of pediatric low-grade gliomas (PLGGs) based on radiomic features extracted from multiparametric MRI. METHODS: 61 patients with PLGGs were included in this retrospective study, which were divided into a training set and an internal validation set at a ratio of 2:1 based on the molecular subgroups or the molecular marker. The patients were classified into low-risk and intermediate/high-risk groups, BRAF fusion positive and negative groups, respectively. We extracted 5929 radiomic features from multiparametric MRI. Thereafter, we removed redundant features, trained random forest models on the training set for predicting the molecular subgroups or the molecular marker, and validated their performance on the internal validation set. The performance of the prediction model was verified by 3-fold cross-validation. RESULTS: We constructed the classification model differentiating low-risk PLGGs from intermediate/high-risk PLGGs using 4 relevant features, with an AUC of 0.833 and an accuracy of 76.2% in the internal validation set. In the prediction model for predicting KIAA1549-BRAF fusion using 4 relevant features, an AUC of 0.818 and an accuracy of 81.0% were achieved in the internal validation set. CONCLUSIONS: The current study demonstrates that MRI radiomics is able to predict molecular subgroups of PLGGs and KIAA1549-BRAF fusion with satisfying sensitivity. TRIAL REGISTRATION: This study was retrospectively registered at clinicaltrials.gov (NCT04217018). SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12885-023-11338-8.