CDIDN: A Registration Model with High Deformation Impedance Capability for Long-Term Tracking of Pulmonary Lesion Dynamics
This work addresses the challenge of accurately tracking pulmonary lesion dynamics over time, which is crucial for early detection and monitoring in medical imaging, though it appears incremental as it builds on existing learning-based registration methods.
The paper tackles the problem of medical CT image registration by focusing on handling local large deformations (LLDs) caused by organ motion and tissue changes, proposing the CDIDN model which shows the best deformation impedance capability and excellent accuracy compared to other learning-based methods.
We study the problem of registration for medical CT images from a novel perspective -- the sensitivity to degree of deformations in CT images. Although some learning-based methods have shown success in terms of average accuracy, their ability to handle regions with local large deformation (LLD) may significantly decrease compared to dealing with regions with minor deformation. This motivates our research into this issue. Two main causes of LLDs are organ motion and changes in tissue structure, with the latter often being a long-term process. In this paper, we propose a novel registration model called Cascade-Dilation Inter-Layer Differential Network (CDIDN), which exhibits both high deformation impedance capability (DIC) and accuracy. CDIDN improves its resilience to LLDs in CT images by enhancing LLDs in the displacement field (DF). It uses a feature-based progressive decomposition of LLDs, blending feature flows of different levels into a main flow in a top-down manner. It leverages Inter-Layer Differential Module (IDM) at each level to locally refine the main flow and globally smooth the feature flow, and also integrates feature velocity fields that can effectively handle feature deformations of various degrees. We assess CDIDN using lungs as representative organs with large deformation. Our findings show that IDM significantly enhances LLDs of the DF, by which improves the DIC and accuracy of the model. Compared with other outstanding learning-based methods, CDIDN exhibits the best DIC and excellent accuracy. Based on vessel enhancement and enhanced LLDs of the DF, we propose a novel method to accurately track the appearance, disappearance, enlargement, and shrinkage of pulmonary lesions, which effectively addresses detection of early lesions and peripheral lung lesions, issues of false enlargement, false shrinkage, and mutilation of lesions.