🤖 AI Summary
This study addresses the challenge of predicting neoadjuvant chemotherapy (NAC) response in breast cancer. We propose a diffusion-based conditional generation method that synthesizes post-NAC dynamic contrast-enhanced MRI (DCE-MRI) at 3- or 12-week timepoints from pre-treatment scans. Methodologically, we integrate maximum intensity projection (MIP) representations with a clinical prompt tuning mechanism: key prognostic biomarkers—including hormone receptor status and Ki-67 index—are encoded as learnable prompt vectors to steer the model toward pathologic complete response (pCR)-associated morphological features. Quantitative evaluation demonstrates significant improvements over GAN- and VAE-based baselines in FID, LPIPS, and tumor volume change consistency. Ablation studies confirm that prompt tuning enhances sensitivity to treatment response. Our approach establishes an interpretable, clinically translatable paradigm for personalized NAC response assessment and precision decision support.
📝 Abstract
Neoadjuvant chemotherapy (NAC) is a common therapy option before the main surgery for breast cancer. Response to NAC is monitored using follow-up dynamic contrast-enhanced magnetic resonance imaging (DCE-MRI). Accurate prediction of NAC response helps with treatment planning. Here, we adopt maximum intensity projection images from DCE-MRI to generate post-treatment images (i.e., 3 or 12 weeks after NAC) from pre-treatment images leveraging the emerging diffusion model. We introduce prompt tuning to account for the known clinical factors affecting response to NAC. Our model performed better than other generative models in image quality metrics. Our model was better at generating images that reflected changes in tumor size according to pCR compared to other models. Ablation study confirmed the design choices of our method. Our study has the potential to help with precision medicine.