CVJul 6

Continual Model Merging with Test-Time Adaptation for Whole-Slide Image Analysis

arXiv:2607.047553.8
Predicted impact top 85% in CV · last 90 daysOriginality Synthesis-oriented
AI Analysis

For computational pathology, this work provides the first systematic evaluation of test-time adaptation for model merging in continual learning, identifying both promise and limitations for rehearsal-free WSI analysis.

This paper benchmarks test-time adaptation-guided model merging for continual whole-slide image classification, showing it achieves strong task-specific performance and knowledge retention without storing historical data, but remains sensitive to task order and distribution shifts.

Model merging offers a practical alternative to conventional continual learning by integrating independently fine-tuned models without retaining previous training data. Recent state-of-the-art model merging methods employ test-time adaptation (TTA-guided merging) to address distribution shifts by adjusting merging-related variables using unlabeled target data. However, these methods have primarily been studied in multi-task or single-target settings, and their behavior under sequential continual learning remains insufficiently understood. We present a benchmark study that maps this family of methods to rehearsal-free continual Whole Slide Image classification and evaluates them against traditional continual-learning approaches. Experiments on six TCGA cancer-subtyping cohorts cover CLASS-IL and TASK-IL scenarios, in-domain and out-of-domain evaluation, and different task orders. The results show that adapting model merging at test time can provide strong task-specific performance and improve retention of previously acquired knowledge without storing historical WSIs. Nevertheless, performance remains sensitive to task order and to the interaction between adaptation on the current distribution and accumulated knowledge. This benchmark identifies model merging with test-time adaptation as a promising direction for continual computational pathology and motivates future methods that balance adaptation to domain shift with explicit preservation of historical knowledge.

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