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Radiomic Based Machine Learning Performance for a Three Class Problem in Neuro-Oncology: Time to Test the Waters?
Sarv Priya1, Yanan Liu2, Caitlin Ward3
1Department of Radiology, University of Iowa Hospitals and Clinics, Iowa City, IA 52242, USA.
Radiomics can differentiate three malignant brain tumors, including glioblastoma (GBM), primary central nervous system lymphoma (PCNSL), and metastatic disease. The T1 contrast-enhanced MRI sequence performed comparably to multiparametric MRI, highlighting its utility.
Area of Science:
- Radiology and Imaging Science
- Oncology
- Medical Artificial Intelligence
Background:
- Previous radiomics studies primarily focused on two-class brain tumor classification, limiting their real-world applicability.
- Differentiating between glioblastoma (GBM), primary central nervous system lymphoma (PCNSL), and metastatic disease using radiomics requires further investigation.
- The impact of MRI sequence selection and tumor subregion segmentation on radiomics model performance is not well-understood.
Purpose of the Study:
- To assess the performance of radiomics in distinguishing between GBM, PCNSL, and metastatic brain tumors.
- To evaluate factors influencing radiomics model performance, including MRI sequence choice and segmentation strategies.
- To compare the utility of single MRI sequences versus multiparametric MRI (MP-MRI) for brain tumor classification.
Main Methods:
- A retrospective analysis of 253 patients with GBM, PCNSL, or metastatic brain tumors.
- Radiomic features were extracted using two pipelines: whole tumor (enhancing + necrotic) and edema masks, and separate enhancing, necrotic, and edema masks.
- Model performance was evaluated using MP-MRI, individual sequences, and the T1 contrast-enhanced (T1-CE) sequence across various model/feature selection combinations.
Main Results:
- The second radiomics pipeline, segmenting distinct tumor subregions, demonstrated high performance (Brier score: 0.311-0.325).
- The Gradient Boosting Regression Model (GBRM) using the full feature set from the T1-CE sequence achieved the best performance.
- Top-performing models showed no significant difference between MP-MRI (AUC 0.910) and T1-CE sequences with (AUC 0.908) or without edema masks (AUC 0.894), indicating T1-CE's standalone efficacy.
Conclusions:
- The T1 contrast-enhanced (T1-CE) MRI sequence alone provides performance comparable to multiparametric MRI (MP-MRI) for differentiating the three most common malignant brain tumors.
- Radiomics models utilizing detailed tumor subregion segmentation (enhancing, necrotic, edema) show superior performance.
- Model performance is influenced by tumor subregion definition and the choice of modeling and feature selection techniques.
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