Author:
Zhao Lian,Shi Liting,Huang Shun-gen,Cai Tian-na,Guo Wan-liang,Gao Xin,Wang Jian
Abstract
Abstract
Background
To identify radiomic features that can predict the pathological type of neuroblastic tumor in children.
Methods
Data on neuroblastic tumors in 104 children were retrospectively analyzed. There were 14 cases of ganglioneuroma, 24 cases of ganglioneuroblastoma, and 65 cases of neuroblastoma. Stratified sampling was used to randomly allocate the cases into the training and validation sets in a ratio of 3:1. The maximum relevance–minimum redundancy algorithm was used to identify the top 10 of two clinical features and 851 radiomic features in portal venous–phase contrast-enhanced computed tomography images. Least absolute shrinkage and selection operator regression was used to classify tumors in two binary steps: first as ganglioneuroma compared to the other two types, then as ganglioneuroblastoma compared to neuroblastoma.
Results
Based on 10 clinical-radiomic features, the classifier identified ganglioneuroma compared to the other two tumor types in the validation dataset with sensitivity of 100.0%, specificity of 81.8%, and an area under the receiver operating characteristic curve (AUC) of 0.875. The classifier identified ganglioneuroblastoma versus neuroblastoma with a sensitivity of 83.3%, a specificity of 87.5%, and an AUC of 0.854. The overall accuracy of the classifier across all three types of tumors was 80.8%.
Conclusion
Radiomic features can help predict the pathological type of neuroblastic tumors in children.
Funder
the Key Research and Development Program of Shandong Province
Key Research and Development Program of Jiangsu Province
Key Research and Development Program (Social Development) of Jiangsu Province
Introductory Project in the Suzhou "Clinical Medicine Expert Team" Program
Suzhou Science and Technology Development (Minsheng Technology) Project
Publisher
Springer Science and Business Media LLC
Subject
Pediatrics, Perinatology and Child Health
Cited by
4 articles.
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