# Ensemble of Pathology Foundation Models for MIDOG 2025 Track 2: Atypical Mitosis Classification

arXiv: https://arxiv.org/abs/2509.02591 · HTML: https://mlsanity.com/paper/2509.02591/

## Key facts

- No citing papers in the map yet (data through 14 Oct 2026).
- Builds on 7 of its 21 references that are in the map.
- First posted on arXiv 29 Aug 2025.

## Builds on (most cited first, 7 of 7)

- [LoRA: Low-Rank Adaptation of Large Language Models](https://mlsanity.com/paper/2106.09685/) (2021)
- [ImageNet-trained CNNs are biased towards texture; increasing shape bias improves accuracy and robustness](https://mlsanity.com/paper/1811.12231/) (2018)
- [Are Convolutional Neural Networks or Transformers more like human vision?](https://mlsanity.com/paper/2105.07197/) (2021)
- [Learning domain-agnostic visual representation for computational pathology using medically-irrelevant style transfer augmentation](https://mlsanity.com/paper/2102.01678/) (2021)
- [Histologic Dataset of Normal and Atypical Mitotic Figures on Human Breast Cancer (AMi-Br)](https://mlsanity.com/paper/2501.04467/) (2025)
- [Benchmarking Deep Learning and Vision Foundation Models for Atypical vs. Normal Mitosis Classification with Cross-Dataset Evaluation](https://mlsanity.com/paper/2506.21444/) (2025)
- [Sk-Unet Model with Fourier Domain for Mitosis Detection](https://mlsanity.com/paper/2109.00957/) (2021)

## Abstract (arXiv)

Mitotic figures are classified into typical and atypical variants, with atypical counts correlating strongly with tumor aggressiveness. Accurate differentiation is therefore essential for patient prognostication and resource allocation, yet remains challenging even for expert pathologists. Here, we leveraged Pathology Foundation Models (PFMs) pre-trained on large histopathology datasets and applied parameter-efficient fine-tuning via low-rank adaptation. In addition, we incorporated ConvNeXt V2, a state-of-the-art convolutional neural network architecture, to complement PFMs. During training, we employed a fisheye transform to emphasize mitoses and Fourier Domain Adaptation using ImageNet target images. Finally, we ensembled multiple PFMs to integrate complementary morphological insights, achieving competitive balanced accuracy on the Preliminary Evaluation Phase dataset.