arXiv subjects

Cecilia Diana-Albelda

Publications and source records attributed to Cecilia Diana-Albelda.

3 recordsLinked to original sources

arXiv2026

CAPS: Clinically-Verifiable Anatomy-Prioritized Synthesis for Missing MRI Imputation in Brain Tumor Segmentation

Multi-parametric MRI is the gold standard for neuro-oncology, yet acquiring complete 4-modality protocols may be unfeasible in real-world clinical practice. When handling missing modalities, existing automated systems force a critical compromise: robust segmenters operate as uninterpretable "black boxes" that bypass image generation, while standard synthesis models often produce blurry reconstructions lacking diagnostic reliability. To address this issue, we propose CAPS, a Clinically-Verifiable Anatomy-Prioritized Synthesis framework that reconciles computational precision with clinical transparency. Our multi-modal generative architecture is driven by a hybrid objective function (L_1 + L_AFP + L_DualDice) that explicitly enforces the preservation of deep anatomical features and strict topological boundaries, rather than relying solely on pixel-wise optimization. Evaluated comprehensively on the BraTS Adult Glioma dataset, the framework achieves superior synthesis fidelity across intensity-based metrics, and demonstrates robust downstream segmentation performance (82.38% mean Dice), successfully restoring verifiable visual context. Furthermore, the framework exhibits exceptional zero-shot cross-domain generalization, maintaining high structural fidelity across completely unseen Meningioma, Pediatric, and Sub-Saharan African cohorts without domain-specific adaptation. Finally, a blinded radiological assessment confirms that our anatomy-aware approach significantly enhances both perceived image quality and clinical utility, providing clinicians with the reliable visual evidence required to trust downstream automated workflows.

eess.IV↗

arXiv2026

Convergent Performance, Divergent Mechanisms in LoRA-Adapted Vision Foundation Models for Brain MRI

Adapting Vision Foundation Models (VFMs) to medical imaging via LoRA has become standard practice, yet model selection is guided almost entirely by downstream task metrics, treating backbones with similar performance as interchangeable. We investigate whether equal performance implies equal internal representational shift. We analyse four ViT-B/16 backbones, DINOv3, SigLIP2, MerMED-FM, and BiomedCLIP, pre-trained with different objectives (self-distillation vs. contrastive vision-language) and on different data domains (natural vs. medical images). We adapt each to brain tumour segmentation and evaluate on six datasets covering both segmentation and Alzheimer's disease classification. Using attention divergence, weight-change analysis, and activation patching, we find that the four models converge to similar segmentation performance (mean Dice 78-81%) through markedly different internal dynamics, yet diverge in cross-task transfer: segmentation adaptation improves Alzheimer's disease classification for DINOv3 but degrades it for the other three backbones. We reveal a dissociation between modification magnitude and causal importance: the most heavily modified layers are not the causally relevant ones, with early-to-mid layers identified as sufficient for segmentation recovery. Restricting LoRA to these layers matches or approaches full-layer segmentation while reducing classification degradation in the three affected backbones, providing a mechanistically grounded strategy that is more parameter-efficient and more robust than standard full-layer adaptation.

cs.CV↗

arXiv2025

GBT-SAM: A Parameter-Efficient Depth-Aware Model for Generalizable Brain tumour Segmentation on mp-MRI

Gliomas are aggressive brain tumors that require accurate imaging-based diagnosis, with segmentation playing a critical role in evaluating morphology and treatment decisions. Manual delineation of gliomas is time-consuming and prone to variability, motivating the use of deep learning to improve consistency and alleviate clinical workload. However, existing methods often fail to fully exploit the information available in multi-parametric MRI (mp-MRI), particularly inter-slice contextual features, and typically require considerable computational resources while lacking robustness across tumor type variations. We present GBT-SAM, a parameter-efficient deep learning framework that adapts the Segment Anything Model (SAM), a large-scale vision model, to volumetric mp-MRI data. GBT-SAM reduces input complexity by selecting fewer than 2.6\% of slices per scan while incorporating all four MRI modalities, preserving essential tumor-related information with minimal cost. Furthermore, our model is trained by a two-step fine-tuning strategy that incorporates a depth-aware module to capture inter-slice correlations and lightweight adaptation layers, resulting in just 6.5M trainable parameters, which is the lowest among SAM-based approaches. GBT-SAM achieves a Dice Score of 93.54 on the BraTS Adult Glioma dataset and demonstrates robust performance on Meningioma, Pediatric Glioma, and Sub-Saharan Glioma datasets. These results highlight GBT-SAM's potential as a computationally efficient and domain-robust framework for brain tumor segmentation using mp-MRI. Our code and models are available at https://github.com/vpulab/med-sam-brain .

eess.IV↗