Evidence map›Paper›PMID 42769520›Full record

ArticleProceedings of SPIE--the International Society for Optical Engineering2026

Evaluating New AI Cell Foundation Models on Challenging Kidney Pathology Cases Unaddressed by Previous Foundation Models.

Runchen Wang, Junlin Guo, Siqi Lu, Ruining Deng, Zhengyi Lu, Yanfan Zhu, Yuechen Yang, Chongyu Qu, Yu Wang, Shilin Zhao and 5 more

Abstract read
In one paragraph

Article in Proceedings of SPIE--the International Society for Optical Engineering, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors.

Runchen WangDepartment of Computer Science, Vanderbilt University, Nashville, TN 37235, USA.
Junlin GuoDepartment of Electrical and Computer Engineering, Vanderbilt University, Nashville, TN 37235, USA.
Siqi LuDepartment of Electrical and Computer Engineering, Vanderbilt University, Nashville, TN 37235, USA.
Ruining DengDepartment of Radiology, Weill Cornell Medicine, New York, NY 10021, USA.
Zhengyi LuDepartment of Electrical and Computer Engineering, Vanderbilt University, Nashville, TN 37235, USA.
Yanfan ZhuDepartment of Computer Science, Vanderbilt University, Nashville, TN 37235, USA.
Yuechen YangDepartment of Computer Science, Vanderbilt University, Nashville, TN 37235, USA.
Chongyu QuDepartment of Electrical and Computer Engineering, Vanderbilt University, Nashville, TN 37235, USA.
Yu WangDepartment of Biostatistics, Vanderbilt University Medical Center, Nashville, TN 37235, USA.
Shilin ZhaoDepartment of Biostatistics, Vanderbilt University Medical Center, Nashville, TN 37235, USA.
Catie ChangDepartment of Computer Science, Vanderbilt University, Nashville, TN 37235, USA.
Mitchell WilkesDepartment of Electrical and Computer Engineering, Vanderbilt University, Nashville, TN 37235, USA.
Mengmeng YinDepartment of Pathology, Microbiology and Immunology, Vanderbilt University Medical Center, Nashville, TN 37235, USA.
Haichun YangDepartment of Pathology, Microbiology and Immunology, Vanderbilt University Medical Center, Nashville, TN 37235, USA.
Yuankai HuoDepartment of Computer Science, Vanderbilt University, Nashville, TN 37235, USA.

Funding

Complementary ex vivo multimodal optical imaging and in vivo Raman spectroscopy to understand tissue dynamicsR01EB033385 · NIBIB · VANDERBILT UNIVERSITY · PI MAHADEVAN-JANSEN, ANITA, REESE, JOHN JEFFREY · 2022 to 2025
$2.6M
AI-empowered 3D Computer Vision and Image-Omics Integration for Digital Kidney HistopathologyR01DK135597 · NIDDK · VANDERBILT UNIVERSITY · PI Yuankai Huo · 2023 to 2026
$2.1M
Dual-wavelength endoscopic Raman probe for eosinophilic esophagitisR01DK132338 · NIDDK · VANDERBILT UNIVERSITY · PI MAHADEVAN-JANSEN, ANITA · 2022 to 2025
$1.7M
NIBIB NIH HHS R01 EB033385NIDDK NIH HHS R01 DK132338NIDDK NIH HHS R01 DK135597
6 · The paper itself

Abstract

Accurate cell nuclei segmentation is critical for downstream tasks in kidney pathology and remains a major challenge due to the morphological diversity and imaging variability of renal tissues. While our prior work has evaluated early-generation AI cell foundation models in this domain, the effectiveness of recent cell foundation models remains unclear. In this study, we benchmark advanced AI cell foundation models (2025), including CellViT++ variants and Cellpose-SAM, against three widely used cell foundation models developed prior to 2024, using a diverse large-scale set of kidney image patches within a human-in-the-loop rating framework. We further performed fusion-based ensemble evaluation and model agreement analysis to assess the segmentation capabilities of the different models. Our results show that CellViT++ [Virchow] yields the highest standalone performance with 40.3% of predictions rated as "Good" on a curated set of 2,091 challenging samples, outperforming all prior models. In addition, our fused model achieves 62.2% "Good" predictions and only 0.4% "Bad", substantially reducing segmentation errors. Notably, the fusion model (2025) successfully resolved the majority of challenging cases that remained unaddressed in our previous study. These findings demonstrate the potential of AI cell foundation model development in renal pathology and provide a curated dataset of challenging samples to support future kidney-specific model refinement.

Indexed as

Cell NucleiEnsemble LearningFoundation ModelHuman-in-the-loopInstance SegmentationKidney Pathology

Identifiers

PMID42769520
PMCPMC13591460

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.