Affiliation:
1. School of Electronic Engineering and Computer Science, Queen Mary University of London, London E1 4NS, UK
Abstract
Brain tumors pose significant health challenges worldwide, with glioblastoma being one of the most aggressive forms. The accurate determination of the O6-methylguanine-DNA methyltransferase (MGMT) promoter methylation status is crucial for personalized treatment strategies. However, traditional methods are labor-intensive and time-consuming. This paper proposes a novel multi-modal approach, BTDNet, that leverages multi-parametric MRI scans, including FLAIR, T1w, T1wCE, and T2 3D volumes, to predict the MGMT promoter methylation status. BTDNet’s main contribution involves addressing two main challenges: the variable volume lengths (i.e., each volume consists of a different number of slices) and the volume-level annotations (i.e., the whole 3D volume is annotated and not the independent slices that it consists of). BTDNet consists of four components: (i) data augmentation (which performs geometric transformations, convex combinations of data pairs, and test-time data augmentation); (ii) 3D analysis (which performs global analysis through a CNN-RNN); (iii) routing (which contains a mask layer that handles variable input feature lengths); and (iv) modality fusion (which effectively enhances data representation, reduces ambiguities, and mitigates data scarcity). The proposed method outperformed state-of-the-art methods in the RSNA-ASNR-MICCAI BraTS 2021 Challenge by at least 3.3% in terms of the F1 score, offering a promising avenue for enhancing brain tumor diagnosis and treatment.
Subject
Fluid Flow and Transfer Processes,Computer Science Applications,Process Chemistry and Technology,General Engineering,Instrumentation,General Materials Science
Cited by
1 articles.
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