Scalable Swin Transformer network for brain tumor segmentation from incomplete MRI modalities.

Artif Intell Med

Department of Computer Science, Johns Hopkins University, Baltimore, 21218, MD, USA. Electronic address:

Published: March 2024

AI Article Synopsis

  • Deep learning methods show promise in improving brain tumor segmentation from MRI data but struggle with incomplete modalities commonly found in clinical settings.
  • The proposed IMSTrans model uses a single encoder from a Swin Transformer architecture for efficient feature extraction and fusion, enhancing performance while maintaining low complexity.
  • Experimental results demonstrate that IMSTrans outperforms the state-of-the-art mmFormer in multiple datasets, achieving higher Dice similarity scores and significantly reducing model complexity with fewer parameters and lower computational demands.

Article Abstract

Background: Deep learning methods have shown great potential in processing multi-modal Magnetic Resonance Imaging (MRI) data, enabling improved accuracy in brain tumor segmentation. However, the performance of these methods can suffer when dealing with incomplete modalities, which is a common issue in clinical practice. Existing solutions, such as missing modality synthesis, knowledge distillation, and architecture-based methods, suffer from drawbacks such as long training times, high model complexity, and poor scalability.

Method: This paper proposes IMSTrans, a novel lightweight scalable Swin Transformer network by utilizing a single encoder to extract latent feature maps from all available modalities. This unified feature extraction process enables efficient information sharing and fusion among the modalities, resulting in efficiency without compromising segmentation performance even in the presence of missing modalities.

Results: Two datasets, BraTS 2018 and BraTS 2020, containing incomplete modalities for brain tumor segmentation are evaluated against popular benchmarks. On the BraTS 2018 dataset, our model achieved higher average Dice similarity coefficient (DSC) scores for the whole tumor, tumor core, and enhancing tumor regions (86.57, 75.67, and 58.28, respectively), in comparison with a state-of-the-art model, i.e. mmFormer (86.45, 75.51, and 57.79, respectively). Similarly, on the BraTS 2020 dataset, our model scored higher DSC scores in these three brain tumor regions (87.33, 79.09, and 62.11, respectively) compared to mmFormer (86.17, 78.34, and 60.36, respectively). We also conducted a Wilcoxon test on the experimental results, and the generated p-value confirmed that our model's performance was statistically significant. Moreover, our model exhibits significantly reduced complexity with only 4.47 M parameters, 121.89G FLOPs, and a model size of 77.13 MB, whereas mmFormer comprises 34.96 M parameters, 265.79 G FLOPs, and a model size of 559.74 MB. These indicate our model, being light-weighted with significantly reduced parameters, is still able to achieve better performance than a state-of-the-art model.

Conclusion: By leveraging a single encoder for processing the available modalities, IMSTrans offers notable scalability advantages over methods that rely on multiple encoders. This streamlined approach eliminates the need for maintaining separate encoders for each modality, resulting in a lightweight and scalable network architecture. The source code of IMSTrans and the associated weights are both publicly available at https://github.com/hudscomdz/IMS2Trans.

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Source
http://dx.doi.org/10.1016/j.artmed.2024.102788DOI Listing

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