Evaluating Cell AI Foundation Models in Kidney Pathology with Human-in-the-Loop Enrichment
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Abstract (arXiv)
Training AI foundation models has emerged as a promising large-scale learning approach for addressing real-world healthcare challenges, including digital pathology. While many of these models have been developed for tasks like disease diagnosis and tissue quantification using extensive and diverse training datasets, their readiness for deployment on some arguably simplest tasks, such as nuclei segmentation within a single organ (e.g., the kidney), remains uncertain. This paper seeks to answer this key question, "How good are we?", by thoroughly evaluating the performance of recent cell foundation models on a curated multi-center, multi-disease, and multi-species external testing dataset. Additionally, we tackle a more challenging question, "How can we improve?", by developing and assessing human-in-the-loop data enrichment strategies aimed at enhancing model performance while minimizing the reliance on pixel-level human annotation. To address the first question, we curated a multicenter, multidisease, and multispecies dataset consisting of 2,542 kidney whole slide images (WSIs). Three state-of-the-art (SOTA) cell foundation models-Cellpose, StarDist, and CellViT-were selected for evaluation. To tackle the second question, we explored data enrichment algorithms by distilling predictions from the different foundation models with a human-in-the-loop framework, aiming to further enhance foundation model performance with minimal human efforts. Our experimental results showed that all three foundation models improved over their baselines with model fine-tuning with enriched data. Interestingly, the baseline model with the highest F1 score does not yield the best segmentation outcomes after fine-tuning. This study establishes a benchmark for the development and deployment of cell vision foundation models tailored for real-world data applications.
Key facts. Cited by 5 papers in the map (data through 14 Oct 2026). Builds on 18 of its 53 references that are in the map. First posted on arXiv 31 Oct 2024.
Builds on
18 of 53 references.
References · 18
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6 more
- 2018Micro-Net: A unified model for segmentation of various objects in microscopy imagescited by 56
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Built on by
Citing papers per year: 2025: 3; 2026: 2.
5 papers.
- 2025DeepAndes: A Self-Supervised Vision Foundation Model for Multi-Spectral Remote Sensing Imagery of the Andescited by 2
- 2025AMA-SAM: Adversarial Multi-Domain Alignment of Segment Anything Model for High-Fidelity Histology Nuclei Segmentationcited by 1
- 2025ZeroReg3D: A Zero-shot Registration Pipeline for 3D Consecutive Histopathology Image Reconstructioncited by 1
- 2026Explainable Pathomics Feature Visualization via Correlation-aware Conditional Feature Editingcited by 0
- 2026Scalable In-Domain Self-Supervised Foundation Model for Dense Representation Transfer in High-Resolution Plant Imagingcited by 0
- 2026Scalable In-Domain Self-Supervised Foundation Model for Dense Representation Transfer in High-Resolution Plant Imaging26 Sep 2026
- 2026Explainable Pathomics Feature Visualization via Correlation-aware Conditional Feature Editing5 Feb 2026
- 2025ZeroReg3D: A Zero-shot Registration Pipeline for 3D Consecutive Histopathology Image Reconstruction27 Jun 2025
- 2025DeepAndes: A Self-Supervised Vision Foundation Model for Multi-Spectral Remote Sensing Imagery of the Andes28 Apr 2025
- 2025AMA-SAM: Adversarial Multi-Domain Alignment of Segment Anything Model for High-Fidelity Histology Nuclei Segmentation27 Mar 2025