Toward Reliable AR-Guided Surgical Navigation: Interactive Deformation Modeling with Data-Driven Biomechanics and Prompts

In augmented reality (AR)-guided surgical navigation, preoperative organ models are superimposed onto the patient's intraoperative anatomy to visualize critical structures such as vessels and tumors. Accurate deformation modeling is essential to maintain the reliability of AR overlays by ensuring alignment between preoperative models and the dynamically changing anatomy. Although the finite element method (FEM) offers physically plausible modeling, its high computational cost limits intraoperative applicability. Moreover, existing algorithms often fail to handle large anatomical changes, such as those induced by pneumoperitoneum or ligament dissection, leading to inaccurate anatomical correspondences and compromised AR guidance. To address these challenges, we propose a data-driven biomechanics algorithm that preserves FEM-level accuracy while improving computational efficiency. In addition, we introduce a novel human-in-the-loop mechanism into the deformation modeling process. This enables surgeons to interactively provide prompts to correct anatomical misalignments, thereby incorporating clinical expertise and allowing the model to adapt dynamically to complex surgical scenarios. Experiments on a publicly available dataset demonstrate that our algorithm achieves a mean target registration error of 3.42 mm. Incorporating surgeon prompts through the interactive framework further reduces the error to 2.78 mm, surpassing state-of-the-art methods in volumetric accuracy. These results highlight the ability of our framework to deliver efficient and accurate deformation modeling while enhancing surgeon-algorithm collaboration, paving the way for safer and more reliable computer-assisted surgeries.

Zero-Shot and Few-Shot Learning for Lung Cancer Multi-Label Classification using Vision Transformer

Lung cancer is the leading cause of cancer-related death worldwide. Lung adenocarcinoma (LUAD) and lung squamous cell carcinoma (LUSC) are the most common histologic subtypes of non-small-cell lung cancer (NSCLC). Histology is an essential tool for lung cancer diagnosis. Pathologists make classifications according to the dominant subtypes. Although morphology remains the standard for diagnosis, significant tool needs to be developed to elucidate the diagnosis. In our study, we utilize the pre-trained Vision Transformer (ViT) model to classify multiple label lung cancer on histologic slices (from dataset LC25000), in both Zero-Shot and Few-Shot settings. Then we compare the performance of Zero-Shot and Few-Shot ViT on accuracy, precision, recall, sensitivity and specificity. Our study show that the pre-trained ViT model has a good performance in Zero-Shot setting, a competitive accuracy ($99.87\%$) in Few-Shot setting ({epoch = 1}) and an optimal result ($100.00\%$ on both validation set and test set) in Few-Shot seeting ({epoch = 5}).