Joon Jang

Han Jang, Junhyeok Lee, Heeseong Eum et al.

Precise molecular subtyping of gliomas, including isocitrate dehydrogenase (IDH) mutation and 1p/19q codeletion, directly guides surgical and therapeutic decisions, yet currently relies on invasive tissue sampling. Deep learning on structural MRI has emerged as a non-invasive alternative, but anatomy-only approaches cannot capture the hemodynamic signatures that distinguish molecular subtypes. Radiogenomics based on dynamic susceptibility contrast (DSC) MRI holds immense potential for non-invasively characterizing glioma molecular subtypes, yet clinical deployment has been hindered by inter-site variability and the limitations of voxel-wise analysis. We introduce HiPerfGNN, a framework that first learns discrete hemodynamic representations from raw time-intensity curves using a vector-quantized variational autoencoder (VQ-VAE). These quantized perfusion codes define coarse-level graph nodes representing functional tumor habitats, each of which is hierarchically subdivided into fine-level subregions guided by structural MRI. A hierarchical graph neural network then propagates information across scales for molecular prediction. On an internal cohort (n=475), the model achieved AUCs of 0.96 (IDH), 0.89 (1p/19q), and 0.84 (WHO grade), and maintained robust IDH performance (AUC 0.89) on an independent external cohort (n=397) without recalibration. Gradient-based saliency analysis confirms biologically grounded attention patterns aligned with known glioma pathophysiology. Our results demonstrate the added value of integrating perfusion dynamics into radiogenomic pipelines for glioma molecular subtyping. Code is available at https://github.com/janghana/HiPerfGNN.

Junhyeok Lee, Hyunwoong Kim, Hyungjin Chung et al.

Image-to-Image translation models can help mitigate various challenges inherent to medical image acquisition. Latent diffusion models (LDMs) leverage efficient learning in compressed latent space and constitute the core of state-of-the-art generative image models. However, this efficiency comes with a trade-off, potentially compromising crucial pixel-level detail essential for high-fidelity medical images. This limitation becomes particularly critical when generating clinically significant structures, such as lesions, which often occupy only a small portion of the image. Failure to accurately reconstruct these regions can severely impact diagnostic reliability and clinical decision-making. To overcome this limitation, we propose a novel post-training framework for LDMs in medical image-to-image translation by incorporating lesion-aware medical pixel space objectives. This approach is essential, as it not only enhances overall image quality but also improves the precision of lesion delineation. We evaluate our framework on brain CT-to-MRI translation in acute ischemic stroke patients, where early and accurate diagnosis is critical for optimal treatment selection and improved patient outcomes. While diffusion MRI is the gold standard for stroke diagnosis, its clinical utility is often constrained by high costs and low accessibility. Using a dataset of 817 patients, we demonstrate that our framework improves overall image quality and enhances lesion delineation when synthesizing DWI and ADC images from CT perfusion scans, outperforming existing image-to-image translation models. Furthermore, our post-training strategy is easily adaptable to pre-trained LDMs and exhibits substantial potential for broader applications across diverse medical image translation tasks.