📝 SummarXiv

Abstract

The MIDOG 2025 challenge extends prior work on mitotic figure detection by introducing a new Track 2 on atypical mitosis classification. This task aims to distinguish normal from atypical mitotic figures in histopathology images, a clinically relevant but highly imbalanced and cross-domain problem. We investigated two complementary backbones: (i) ConvNeXt-Small, pretrained on ImageNet, and (ii) a histopathology-specific ViT from Lunit trained via self-supervision. To address the strong prevalence imbalance (9408 normal vs. 1741 atypical), we synthesized additional atypical examples to approximate class balance and compared models trained with real-only vs. real+synthetic data. Using five-fold cross-validation, both backbones reached strong performance (mean AUROC approximately 95 percent), with ConvNeXt achieving slightly higher peaks while Lunit exhibited greater fold-to-fold stability. Synthetic balancing, however, did not lead to consistent improvements. On the organizers' preliminary hidden test set, explicitly designed as an out-of-distribution debug subset, ConvNeXt attained the highest AUROC (95.4 percent), whereas Lunit remained competitive on balanced accuracy. These findings suggest that both ImageNet and domain-pretrained backbones are viable for atypical mitosis classification, with domain-pretraining conferring robustness and ImageNet pretraining reaching higher peaks, while naive synthetic balancing has limited benefit. Full hidden test set results will be reported upon challenge completion.