Evidence map›Paper›PMID 39087085›Full record

ArticleJournal of medical imaging (Bellingham, Wash.)2024

Transformation from hematoxylin-and-eosin staining to Ki-67 immunohistochemistry digital staining images using deep learning: experimental validation on the labeling index.

Cunyuan Ji, Kengo Oshima, Takumi Urata, Fumikazu Kimura, Keiko Ishii, Takeshi Uehara, Kenji Suzuki, Saori Takeyama, Masahiro Yamaguchi

Abstract read
In one paragraph

Article in Journal of medical imaging (Bellingham, Wash.), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Cunyuan JiTokyo Institute of Technology, School of Engineering, Department of Information and Communications Engineering, Yokohama, Japan.ORCID https://orcid.org/0009-0001-2801-7408
Kengo OshimaShinshu University, School of Health Sciences, Department of Biomedical Laboratory Sciences, Matsumoto, Japan.ORCID https://orcid.org/0000-0001-6045-3296
Takumi UrataTokyo Institute of Technology, School of Engineering, Department of Information and Communications Engineering, Yokohama, Japan.ORCID https://orcid.org/0009-0001-3512-4527
Fumikazu KimuraShinshu University, School of Health Sciences, Department of Biomedical Laboratory Sciences, Matsumoto, Japan.
Keiko IshiiOkaya City Hospital, Division of Diagnostic Pathology, Okaya, Japan.
Takeshi UeharaShinshu University, School of Medicine, Department of Laboratory Medicine, Matsumoto, Japan.
Kenji SuzukiTokyo Institute of Technology, Institute of Innovative Research, Biomedical AI Research Unit, Yokohama, Japan.
Saori TakeyamaTokyo Institute of Technology, School of Engineering, Department of Information and Communications Engineering, Yokohama, Japan.ORCID https://orcid.org/0000-0002-8282-2491
Masahiro YamaguchiTokyo Institute of Technology, School of Engineering, Department of Information and Communications Engineering, Yokohama, Japan.ORCID https://orcid.org/0000-0003-1001-4505

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: Endometrial cancer (EC) is one of the most common types of cancer affecting women. While the hematoxylin-and-eosin (H&E) staining remains the standard for histological analysis, the immunohistochemistry (IHC) method provides molecular-level visualizations. Our study proposes a digital staining method to generate the hematoxylin-3,3'-diaminobenzidine (H-DAB) IHC stain of Ki-67 for the whole slide image of the EC tumor from its H&E stain counterpart. Approach: We employed a color unmixing technique to yield stain density maps from the optical density (OD) of the stains and utilized the U-Net for end-to-end inference. The effectiveness of the proposed method was evaluated using the Pearson correlation between the digital and physical stain's labeling index (LI), a key metric indicating tumor proliferation. Two different cross-validation schemes were designed in our study: intraslide validation and cross-case validation (CCV). In the widely used intraslide scheme, the training and validation sets might include different regions from the same slide. The rigorous CCV validation scheme strictly prohibited any validation slide from contributing to training. Results: The proposed method yielded a high-resolution digital stain with preserved histological features, indicating a reliable correlation with the physical stain in terms of the Ki-67 LI. In the intraslide scheme, using intraslide patches resulted in a biased accuracy (e.g., Conclusions: Our study revealed that molecule-level insights could be obtained from H&E images using deep learning. Furthermore, the improvement brought via OD inference indicated a possible method for creating more generalizable models for digital staining via per-stain analysis.

Indexed as

deep learningdigital stainingKi-67labeling indexwhole slide image

Identifiers

PMID39087085
PMCPMC11287056

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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.