Evidence map›Paper›PMID 41079974›Full record

ArticleJournal of medical imaging (Bellingham, Wash.)2025

Quantification-based explainable artificial intelligence for deep learning decisions: clustering and visualization of quantitative morphometric features in hepatocellular carcinoma discrimination.

Gen Takagi, Saori Takeyama, Tokiya Abe, Akinori Hashiguchi, Michiie Sakamoto, Kenji Suzuki, Masahiro Yamaguchi

Abstract read
In one paragraph

Article in Journal of medical imaging (Bellingham, Wash.), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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

7 authors.

Gen TakagiInstitute of Science Tokyo, School of Engineering, Department of Information and Communications Engineering, Yokohama, Japan.ORCID https://orcid.org/0009-0002-0287-5508
Saori TakeyamaInstitute of Science Tokyo, School of Engineering, Department of Information and Communications Engineering, Yokohama, Japan.ORCID https://orcid.org/0000-0002-8282-2491
Tokiya AbeKeio University School of Medicine, Department of Pathology, Shinjuku, Japan.ORCID https://orcid.org/0000-0003-0665-8834
Akinori HashiguchiKeio University School of Medicine, Department of Pathology, Shinjuku, Japan.ORCID https://orcid.org/0000-0002-6455-071X
Michiie SakamotoKeio University School of Medicine, Department of Pathology, Shinjuku, Japan.
Kenji SuzukiInstitute of Science Tokyo, School of Engineering, Department of Information and Communications Engineering, Yokohama, Japan.ORCID https://orcid.org/0000-0002-3993-8309
Masahiro YamaguchiInstitute of Science Tokyo, 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: Deep learning (DL) is rapidly advancing in computational pathology, offering high diagnostic accuracy but often functioning as a "black box" with limited interpretability. This lack of transparency hinders its clinical adoption, emphasizing the need for quantitative explainable artificial intelligence (QXAI) methods. We propose a QXAI approach to objectively and quantitatively elucidate the reasoning behind DL model decisions in hepatocellular carcinoma (HCC) pathological image analysis. Approach: The proposed method utilizes clustering in the latent space of embeddings generated by a DL model to identify regions that contribute to the model's discrimination. Each cluster is then quantitatively characterized by morphometric features obtained through nuclear segmentation using HoverNet and key feature selection with LightGBM. Statistical analysis is performed to assess the importance of selected features, ensuring an interpretable relationship between morphological characteristics and classification outcomes. This approach enables the quantitative interpretation of which regions and features are critical for the model's decision-making, without sacrificing accuracy. Results: Experiments on pathology images of hematoxylin-and-eosin-stained HCC tissue sections showed that the proposed method effectively identified key discriminatory regions and features, such as nuclear size, chromatin density, and shape irregularity. The clustering-based analysis provided structured insights into morphological patterns influencing classification, with explanations evaluated as clinically relevant and interpretable by a pathologist. Conclusions: Our QXAI framework enhances the interpretability of DL-based pathology analysis by linking morphological features to classification decisions. This fosters trust in DL models and facilitates their clinical integration.

Indexed as

artificial intelligencecomputer visionimage analysis

Identifiers

PMID41079974
PMCPMC12513858

What OpenQuestion holds

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Registered trials

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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.