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Kalina P. Slavkova

Publications and source records attributed to Kalina P. Slavkova.

3 recordsLinked to original sources

Foundation model embeddings capture pre-diagnostic changes on screening mammograms

Foundation model embeddings of screening mammograms may encode pre-diagnostic tissue change without task-specific adaptation. We tested whether embeddings move faster along a data-derived "cancer direction" in women later biopsied for cancer than in matched screen-negative controls, and whether this depends on pretraining domain. We studied 1,773 biopsied women (785 malignant, 988 biopsy-negative) and 1,773 matched controls, each with at least two annual screening exams before their index exam. An identical pipeline was applied to four 2D models: Mammo-CLIP (MC, out-of-distribution mammography), HOPPR (in-distribution mammography), MedImageInsight (MII, general medical imaging), and BiomedCLIP (biomedical vision-language pretraining on literature figures). Breast-level embeddings quantified longitudinal movement along the cancer direction. We compared cases and controls using a between-patient design with complementary mixed-effects analysis, and biopsied versus healthy contralateral breasts within patients. Under matched modality in MII embedding space, malignant cases drifted significantly faster than controls in the first two screening intervals preceding the index exam; biopsy-negative cases showed significance only in the first. MC differences were significant in the first interval for both biopsy groups. Within-patient comparisons showed a broadly similar pattern, with MC significance extending to the second interval in both groups and HOPPR showing significance at interval 1. BiomedCLIP showed no significant differences in either design or biopsy group. Overall, directional embedding velocity emerges as a property of clinically grounded rather than general biomedical pretraining, showing that foundation model embeddings can encode pre-diagnostic mammographic change without task-specific adaptation.

cs.CV↗

HOPPR Medical-Grade Platform for Medical Imaging AI

Technological advances in artificial intelligence (AI) have enabled the development of large vision language models (LVLMs) that are trained on millions of paired image and text samples. Subsequent research efforts have demonstrated great potential of LVLMs to achieve high performance in medical imaging use cases (e.g., radiology report generation), but there remain barriers that hinder the ability to deploy these solutions broadly. These include the cost of extensive computational requirements for developing large scale models, expertise in the development of sophisticated AI models, and the difficulty in accessing substantially large, high-quality datasets that adequately represent the population in which the LVLM solution is to be deployed. The HOPPR Medical-Grade Platform addresses these barriers by providing powerful computational infrastructure, a suite of foundation models on top of which developers can fine-tune for their specific use cases, and a robust quality management system that sets a standard for evaluating fine-tuned models for deployment in clinical settings. The HOPPR Platform has access to millions of imaging studies and text reports sourced from hundreds of imaging centers from diverse populations to pretrain foundation models and enable use case-specific cohorts for fine-tuning. All data are deidentified and securely stored for HIPAA compliance. Additionally, developers can securely host models on the HOPPR platform and access them via an API to make inferences using these models within established clinical workflows. With the Medical-Grade Platform, HOPPR's mission is to expedite the deployment of LVLM solutions for medical imaging and ultimately optimize radiologist's workflows and meet the growing demands of the field.

cs.CL↗

An untrained deep learning method for reconstructing dynamic magnetic resonance images from accelerated model-based data

The purpose of this work is to implement physics-based regularization as a stopping condition in tuning an untrained deep neural network for reconstructing MR images from accelerated data. The ConvDecoder neural network was trained with a physics-based regularization term incorporating the spoiled gradient echo equation that describes variable-flip angle (VFA) data. Fully-sampled VFA k-space data were retrospectively accelerated by factors of R={8,12,18,36} and reconstructed with ConvDecoder (CD), ConvDecoder with the proposed regularization (CD+r), locally low-rank (LR) reconstruction, and compressed sensing with L1-wavelet regularization (L1). Final images from CD+r training were evaluated at the \emph{argmin} of the regularization loss; whereas the CD, LR, and L1 reconstructions were chosen optimally based on ground truth data. The performance measures used were the normalized root-mean square error, the concordance correlation coefficient (CCC), and the structural similarity index (SSIM). The CD+r reconstructions, chosen using the stopping condition, yielded SSIMs that were similar to the CD (p=0.47) and LR SSIMs (p=0.95) across R and that were significantly higher than the L1 SSIMs (p=0.04). The CCC values for the CD+r T1 maps across all R and subjects were greater than those corresponding to the L1 (p=0.15) and LR (p=0.13) T1 maps, respectively. For R > 12 (<4.2 minutes scan time), L1 and LR T1 maps exhibit a loss of spatially refined details compared to CD+r. We conclude that the use of an untrained neural network together with a physics-based regularization loss shows promise as a measure for determining the optimal stopping point in training without relying on fully-sampled ground truth data.

eess.IV↗