Amide proton transfer MRI-based radiomic signatures for molecular subgrouping of pediatric medulloblastoma
Motivation: Medulloblastoma (MB) is classified into different molecular (WNT, SHH, Group 3, and Group 4) subgroups. Accurate identification of molecular subgroups provides clinical value to the diagnosis of MB. Goal(s): We aim to combine APT MRI and radiomic analysis to establish signatures for distinguishing molecular subgroups of pediatric medulloblastoma. Approach: Fifty newly diagnosed pediatric patients with medulloblastoma were enrolled in this study. Radiomic features were extracted from APT-related metrics to differentiate MB subgroups. Results: APT MRI-based radiomic signatures exhibited favorable performance in identifying WNT, SHH, Group 3, and Group 4 subgroups with AUCs ≥ 0.91. Impact: Our research findings demonstrate that amide proton transfer MRI-based radiomic analysis offers a noninvasive and cost-effective method to distinguish molecular subgroups and holds great potential in providing valuable clinical insights for the diagnosis of pediatric medulloblastoma patients.
Authors
- Feng Hua Zhao (ORCID: https://orcid.org/0000-0003-4793-7135)
- Kannie W. Y. Chan (ORCID: https://orcid.org/0000-0002-7315-1550)
- Zhipeng Shen (ORCID: https://orcid.org/0000-0002-6537-6098)
- Yi Zhang (ORCID: https://orcid.org/0000-0002-5867-9322)
- Junjie Wen (ORCID: https://orcid.org/0009-0002-6629-434X)
- Xiaohui Ma
- Hongxi Zhang (ORCID: https://orcid.org/0000-0002-6335-010X)
- Xinchun Chen (ORCID: https://orcid.org/0000-0002-2101-9013)
- Weibo Chen (ORCID: https://orcid.org/0000-0002-4727-3642)
Publication Details
- Journal
- Proceedings on CD-ROM - International Society for Magnetic Resonance in Medicine. Scientific Meeting and Exhibition/Proceedings of the International Society for Magnetic Resonance in Medicine, Scientific Meeting and Exhibition
- Published
- 2024-11-26
- DOI
- https://doi.org/10.58530/2024/2397
- Primary Topic
- Radiopharmaceutical Chemistry and Applications
- Type
- article
- Field-Weighted Citation Impact
- 0.00