Domain Generalization for Endoscopic Image Segmentation by Disentangling Style-Content Information and SuperPixel Consistency
This work addresses the domain gap issue in medical imaging for gastrointestinal cancer monitoring, offering an incremental improvement over existing methods to enhance segmentation accuracy across modalities.
The paper tackles the problem of domain generalization for endoscopic image segmentation across different imaging modalities, proposing a method that combines style-content disentanglement with superpixel consistency to improve performance, resulting in improvements of up to 18% over baseline and state-of-the-art methods on polyp datasets and a 2% gain on Barrett's Esophagus data.
Frequent monitoring is necessary to stratify individuals based on their likelihood of developing gastrointestinal (GI) cancer precursors. In clinical practice, white-light imaging (WLI) and complementary modalities such as narrow-band imaging (NBI) and fluorescence imaging are used to assess risk areas. However, conventional deep learning (DL) models show degraded performance due to the domain gap when a model is trained on one modality and tested on a different one. In our earlier approach, we used a superpixel-based method referred to as "SUPRA" to effectively learn domain-invariant information using color and space distances to generate groups of pixels. One of the main limitations of this earlier work is that the aggregation does not exploit structural information, making it suboptimal for segmentation tasks, especially for polyps and heterogeneous color distributions. Therefore, in this work, we propose an approach for style-content disentanglement using instance normalization and instance selective whitening (ISW) for improved domain generalization when combined with SUPRA. We evaluate our approach on two datasets: EndoUDA Barrett's Esophagus and EndoUDA polyps, and compare its performance with three state-of-the-art (SOTA) methods. Our findings demonstrate a notable enhancement in performance compared to both baseline and SOTA methods across the target domain data. Specifically, our approach exhibited improvements of 14%, 10%, 8%, and 18% over the baseline and three SOTA methods on the polyp dataset. Additionally, it surpassed the second-best method (EndoUDA) on the Barrett's Esophagus dataset by nearly 2%.