Francesco Tortorella

Marc Aubreville, Jonas Ammeling, Sweta Banerjee et al.

Automated mitosis detection is a well-established task in computational pathology. While previous benchmarks focused on scanner-induced domain shift, clinical "real-world" application requires models to be robust across the vast variance to be expected in the histological landscape. The MItosis DOmain Generalization (MIDOG) 2025 challenge was designed to evaluate algorithmic performance across unprecedented biological and contextual diversity. We curated a test dataset of 365 cases, encompassing 12 distinct human, canine and feline tumor types, digitized across multiple scanning platforms. Moving beyond hand-selected hotspots, the challenge required detection also in random tissue areas (representative of the whole slide detection situation) and challenging areas (areas rich in hard negatives). In the second track, we introduced the classification of atypical mitotic figures (AMFs). There were 18 teams submitting to the detection track, with F1 scores ranging up to 0.740. In the AMF detection track, we had 21 submissions with balanced accuracy values up to 0.908. Our analysis reveals that while most models perform reliably in traditional hotspots, significant performance degradation occurs in challenging ROIs, where false positive rates tripled. Furthermore, performance varied significantly across the 12 tumor types, highlighting "blind spots" in current state-of-the-art architectures when encountering rare or highly pleomorphic malignancies. Moreover, we evaluated the effectiveness of ensembling and found a mean increases of 1.5 and 1.3 percentage points in F1 score and balanced accuracy, respectively. In contrast, TTA showed no relevant improvement. MIDOG 2025 demonstrates that "in the wild" mitosis detection remains a significant hurdle. The transition from hotspot-only evaluation to a multi-contextual framework provides a more realistic proxy for clinical reliability.

Gennaro Percannella, Mattia Sarno, Francesco Tortorella et al.

Recognizing atypical mitotic figures in histopathology images allows physicians to correctly assess tumor aggressiveness. Although machine learning models could be exploited for automatically performing such a task, under domain shift these models suffer from significative performance drops. In this work, an approach based on multi-task learning is proposed for addressing this problem. By exploiting auxiliary tasks, correlated to the main classification task, the proposed approach, submitted to the track 2 of the MItosis DOmain Generalization (MIDOG) challenge, aims to aid the model to focus only on the object to classify, ignoring the domain varying background of the image. The proposed approach shows promising performance in a preliminary evaluation conducted on three distinct datasets, i.e., the MIDOG 2025 Atypical Training Set, the Ami-Br dataset, as well as the preliminary test set of the MIDOG25 challenge.

Gennaro Percannella, Mattia Sarno, Francesco Tortorella et al.

Mitosis detection in histopathology images plays a key role in tumor assessment. Although machine learning algorithms could be exploited for aiding physicians in accurately performing such a task, these algorithms suffer from significative performance drop when evaluated on images coming from domains that are different from the training ones. In this work, we propose a Mamba-based approach for mitosis detection under domain shift, inspired by the promising performance demonstrated by Mamba in medical imaging segmentation tasks. Specifically, our approach exploits a VM-UNet architecture for carrying out the addressed task, as well as stain augmentation operations for further improving model robustness against domain shift. Our approach has been submitted to the track 1 of the MItosis DOmain Generalization (MIDOG) challenge. Preliminary experiments, conducted on the MIDOG++ dataset, show large room for improvement for the proposed method.