mlsanityData to 14 Oct 2026

Evaluating Cell AI Foundation Models in Kidney Pathology with Human-in-the-Loop Enrichment

arXiv 2411.00078 ↗First posted 31 Oct 2024cs.CV cs.AI eess.IVcited by 5

Not on the map. Why?

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

  1. 2017Mask R-CNNcited by 7,277
  2. 2021On the Opportunities and Risks of Foundation Modelscited by 4,033
  3. 2017A Survey on Deep Learning in Medical Image Analysiscited by 1,186
  4. 2023Medical SAM Adapter: Adapting Segment Anything Model for Medical Image Segmentationcited by 490
  5. 2018HoVer-Net: Simultaneous Segmentation and Classification of Nuclei in Multi-Tissue Histology Imagescited by 388
  6. 2022Scaling Vision Transformers to Gigapixel Images via Hierarchical Self-Supervised Learningcited by 359
  7. 2023Segment Anything Model for Medical Image Analysis: an Experimental Studycited by 291
  8. 2023Segment Anything in Medical Imagescited by 227
  9. 2023Segment Anything Model (SAM) for Digital Pathology: Assess Zero-shot Segmentation on Whole Slide Imagingcited by 161
  10. 2023CellViT: Vision Transformers for Precise Cell Segmentation and Classificationcited by 108
  11. 2021Lizard: A Large-Scale Dataset for Colonic Nuclear Instance Segmentation and Classificationcited by 89
  12. 2024VISTA3D: A Unified Segmentation Foundation Model For 3D Medical Imagingcited by 64
6 more
  1. 2018Micro-Net: A unified model for segmentation of various objects in microscopy imagescited by 56
  2. 2021CPP-Net: Context-aware Polygon Proposal Network for Nucleus Segmentationcited by 32
  3. 2022Nuclei instance segmentation and classification in histopathology images with StarDistcited by 31
  4. 2024Foundation Models for Biomedical Image Segmentation: A Surveycited by 28
  5. 2024HATs: Hierarchical Adaptive Taxonomy Segmentation for Panoramic Pathology Image Analysiscited by 9
  6. 2022Nuclei & Glands Instance Segmentation in Histology Images: A Narrative Reviewcited by 3

Built on by

Cited by year (2026 to 14 Oct)

Citing papers per year: 2025: 3; 2026: 2.

5 papers.