Pretext Matters: An Empirical Study of SSL Methods in Medical Imaging
Organizations: Biomedical AI Research Lab, University of California, Los Angeles, Los Angeles, CA, USA · Department of Radiology, University of California, Los Angeles, Los Angeles, CA, USA · Department of Bioengineering, University of California, Los Angeles, Los Angeles, CA, USA · Department of Electrical and Computer Engineering, University of California, Los Angeles, Los Angeles, CA, USA ·
Abstract
Though self-supervised learning (SSL) has demonstrated incredible ability to learn robust representations from unlabeled data, the choice of optimal SSL strategy can lead to vastly different performance outcomes in specialized domains. Joint embedding architectures (JEAs) and joint embedding predictive architectures (JEPAs) have shown robustness to noise and strong semantic feature learning compared to pixel reconstruction-based SSL methods, leading to widespread adoption in medical imaging. However, no prior work has systematically investigated which SSL objective is better aligned with the spatial organization of clinically relevant signal. In this work, we empirically investigate how the choice of SSL method impacts the learned representations in medical imaging. We select two representative imaging modalities characterized by unique noise profiles: ultrasound and histopathology. When informative signal is spatially localized, as in histopathology, JEAs are more effective due to their view-invariance objective. In contrast, when diagnostically relevant information is globally structured, such as the macroscopic anatomy present in liver ultrasounds, JEPAs are optimal. These differences are especially evident in the clinical relevance of the learned features, as independently validated by board-certified radiologists and pathologists. Together, our results provide a framework for matching SSL objectives to the structural and noise properties of medical imaging modalities.
Figures & tables
| Ultrasound | Histopathology | ||
| Dataset | Task | Dataset | Task |
| MMOTU | Ovarian Tumor | CPTAC-Lung | LUAD vs LSCC |
| AUL | Liver Mass Malignancy | PLCO-Lung | LUAD vs LSCC |
| TN5000 | Thyroid Tumor | PLCO-Breast | Breast Cancer Subtype |
| Fatty Liver | Hepatic Steatosis (NAFLD) | Ovarian | Ovarian Cancer Subtype |
| POCUS | Lung Pathology | PANDA | Prostate Biopsy ISUP Grade |
| MAE | DINOv3 | I-JEPA | ||||
| Dataset | AUROC (%) | F1 (%) | AUROC (%) | F1 (%) | AUROC (%) | F1 (%) |
| MMOTU | 78.43 0.12 | 38.04 1.4 | 84.57 0.07 | 50.31 0.65 | 82.59 0.06 | 42.03 0.58 |
| AUL | 81.86 0.21 | 62.52 2.1 | 86.77 0.23 | 66.33 0.52 | 86.47 0.21 | 64.71 0.81 |
| TN5000 | 69.88 0.2 | 58.25 2.2 | 72.36 0.42 | 63.34 1.5 | 75.60 0.12 | 65.83 1.6 |
| Fatty Liver | 65.89 0.6 | 50.76 5.7 | 86.66 1.5 | 64.06 1.7 | 98.70 0.26 | 92.80 1.2 |
| POCUS | 96.12 0.19 | 91.01 0.11 | 99.49 0.07 | 94.00 0.19 | 97.18 0.06 | 90.48 0.52 |
| MAE | DINOv3 | I-JEPA | ||||
| Dataset | AUROC (%) | F1 (%) | AUROC (%) | F1 (%) | AUROC (%) | F1 (%) |
| CPTAC-Lung | 77.1 4.2 | 27.2 33.3 | 91.4 1.0 | 83.3 1.4 | 54.8 1.3 | 31.6 29.4 |
| PLCO-Lung | 63.8 0.9 | 30.6 13.7 | 82.9 1.3 | 66.8 5.3 | 57.4 8.4 | 21.8 26.7 |
| PLCO-Breast | 49.2 2.2 | 26.5 6.2 | 65.2 1.1 | 38.7 8.5 | 52.3 6.2 | 11.6 8.6 |
| Ovarian | 73.5 0.7 | 34.1 7.3 | 92.0 1.8 | 73.3 2.4 | 55.2 4.3 | 4.5 2.0 |
| PANDA | 81.9 0.2 | 44.2 0.3 | 87.0 0.3 | 53.9 0.8 | 64.0 0.6 | 22.7 1.5 |
Appendix figures & tables9 assets
Supplementary material from the paper’s appendix.
Appendix
| Model | Hyperparameter | Value |
| MAE | ViT | ViT-small |
| Batch size | 256 | |
| Learning rate | ||
| Warmup epochs | 10 | |
| DINOv3 | ViT | ViT-small |
| Batch size | 128 |
Self-Supervised Learning
Self-supervised learning uses structure within unlabeled data to train representations and models for downstream tasks.
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