ZHENGYANG ZHU1, Zehong Cao2, Jianan Zhou1, Meiping Ye1, Huiquan Yang1, Xin Zhang1, Feng Shi2, and Bing Zhang3
1Department of Radiology, Department of Radiology, The Affiliated Drum Tower Hospital of Nanjing University Medical School, Nanjing, China, 2Department of Research and Development, Department of Research and Development, Shanghai United Imaging Intelligence Co., Shanghai, China, 3Department of Radiology, The Affiliated Drum Tower Hospital of Nanjing University Medical School, Nanjing University, Nanjing, China
Synopsis
Keywords: Tumors (Pre-Treatment), Tumor, DCE-MRI, IDH, Glioma, Machine learning
Motivation: IDH mutation status of glioma have important influence on its occurrence and prognosis.
Goal(s): To build radiomics models in DCE-MRI for predicting IDH mutation in adult diffuse gliomas.
Approach: Several groups of features were extracted through multiparametric image: 1) Automatically calculated DCE-MRI metrics; 2) Structural MRI radiomics features, and 3) DCE-MRI radiomics features. Z-score normalization was used for feature normalization. Mann–Whitney U test was used for tumor selection. Stochastic gradient descent was used for machine learning classifier.
Results: We achived an AUC of 0.874 for model combing structural-MRI, DCE-MRI radiomics and automatically-calculated DCE-MRI metrics.
Impact: DCE-MRI
radiomics models demonstrated great potential to predict IDH mutation status in
Gliomas.
Background and Purpose
Gliomas are the most common type of primary
intracranial tumors among the world1. In 2016, the 4th edition of World
Health Organization Classification Criteria of Tumors of the Central Nervous
System Tumor (WHO CNS4) first introduced iso-citrate dehydrogenase (IDH)
mutation and 1p19q co-deletion status as diagnostic molecular markers for adult
diffuse gliomas2. In the latest edition WHO CNS5, Adult diffuse gliomas
consist of three subtypes: Glioblastoma, IDH wild type, Astrocytoma, IDH mutant
and Oligodendroglioma, IDH mutant with 1p19q co-delated3. IDH mutation is important for patient management an prognoisis prediction.
Dynamic contrast-enhanced MRI (DCE-MRI) can depict perfusion and microcirculation of tumors4. The aim of this research was to build radiomics
models in DCE-MRI for predicting isocitrate
dehydrogenase (IDH) mutation in adult diffuse gliomas. Method
Patients diagnosed as adult diffuse glioma between September
2018 and September 2022 in our hospital were included. All patients underwent examination before surgery in a 3.0T MR scanner
(uMR790, United Imaging Healthcare). IDH mutation status were determined by either
immunohistochemistry or Sanger sequencing of tumor sample after surgery.
DCE-MRI was performed after Gadodiamide injection
(0.2mL/kg, 3.5mL/s).
DCE-MRI metrics Ktrans, Kep, Ve, Vp, and iAUC were
obtained through extended Tofts model. ADC map was obtained from DWI. Clinically
obtained DCE-MRI and DWI metric values combined with Age and Sex were included as
clinical indices.
Region-of-interests
(ROI) of Tumor Core (TC) and Whole Tumor (WT) were automatically delineated on
T1CE and T2WI using a pretrained deep learning model. The ROI were registered to
DCE-MRI and DWI metrics. Several groups of features were extracted through
multiparametric image: 1) Automatically calculated DCE-MRI metrics; 2) Structural
MRI radiomics features, and 3) DCE-MRI radiomics features. Z-score normalization
was used for feature normalization. Mann–Whitney U test was used for tumor
selection. Stochastic gradient descent was used for machine learning classifier.
Performance of different models was quantified using area under receiver
operating characteristic curve (AUC).Results
A total of
142 patients were included, in which 89 patients are IDH-wildtype. Model-wise
AUCs were 0.587 for clinical Index, 0.676 for automatically-calculated DCE metrics,
0.774 for structural-MRI radiomics, 0.791 for DCE-MRI radiomics, 0.841 for combined
structural-MRI and DCE-MRI radiomics, and 0.874 for combined structural-MRI,
DCE-MRI radiomics and automatically-calculated DCE-MRI metrics.Conclusion
DCE-MRI radiomics models demonstrated great potential to predict IDH
mutation status in Gliomas.Acknowledgements
No acknowledgement found.References
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