Evidence map›Paper›PMID 42135447›Full record

ArticleNPJ digital medicine2026

A human-in-the-loop explanation framework for morphologically transparent AI predictions from whole-slide images.

Peiliang Lou, Yitan Zhu, Nicholas Chia, Roopa Kumari, William Yang, Yan Wang, Brenna C Novotny, Stacey J Winham, Ruifeng Guo, Ellen L Goode and 4 more

Abstract read
In one paragraph

Article in NPJ digital medicine, 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
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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

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

14 authors.

Peiliang LouDivision of Computational Biology, Mayo Clinic, Rochester, MN, USA.
Yitan ZhuDivision of Data Science and Learning, Argonne National Laboratory, Lemont, IL, USA.
Nicholas ChiaDivision of Data Science and Learning, Argonne National Laboratory, Lemont, IL, USA.
Roopa KumariDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
William YangDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
Yan WangDepartment of Pathology, Second People's Hospital of Wuhu, Anhui, China.
Brenna C NovotnyDivision of Computational Biology, Mayo Clinic, Rochester, MN, USA.
Stacey J WinhamDivision of Computational Biology, Mayo Clinic, Rochester, MN, USA.
Ruifeng GuoDivision of Anatomic Pathology, Department of Laboratory Medicine and Pathology, Mayo Clinic, Jacksonville, FL, USA.
Ellen L GoodeDivision of Computational Biology, Mayo Clinic, Rochester, MN, USA.
Yajue HuangDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA. Huang.Yajue@mayo.edu.
Wenchao HanDivision of Computational Pathology and Informatics, Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
Tianshu FengDepartment of Systems Engineering and Operations Research, George Mason University, Fairfax, VA, USA.
Chen WangDivision of Computational Biology, Mayo Clinic, Rochester, MN, USA. wang.chen@mayo.edu.

Funding

Women's Cancer ProgramP30CA015083 · NCI · MAYO CLINIC ROCHESTER · PI Lila J. Rutten · 1985 to 2026
$151.3M
Use of microfluidic tumor cultures to enable clinical trials of therapies for ovarian cancerP50CA136393 · NCI · MAYO CLINIC ROCHESTER · PI SCOTT H KAUFMANN · 2009 to 2026
$37.0M
Relating Molecular Subgroups of Endometriosis-Associated Ovarian Cancers to Survival and RiskR01CA248288 · NCI · MAYO CLINIC ROCHESTER · PI Stacey J Winham · 2021 to 2026
$4.8M
Mayo Clinic NCI R01 CA248288NCI NIH HHS P30 CA015083NCI NIH HHS P50 CA136393NCI NIH HHS R01 CA248288
6 · The paper itself

Abstract

Deep learning models enable the prediction of clinical endpoints from whole-slide images (WSIs), but many such models function as "black boxes", lacking transparency about whether and which histomorphological patterns drive their predictions, hindering interpretability and clinical adoption. Here we propose a human-in-the-loop explanation framework, MorphoXAI, which provides both local and global interpretability for deep learning models by incorporating human-expert interpretations. At the global level, it reveals the histomorphological patterns on which the model consistently relies to distinguish between classes of WSIs, as well as the patterns associated with confusion between classes. At the local level, it indicates which of these patterns are used in the prediction of an individual WSI and which regions within the slide correspond to such patterns. We validated our method across multiple deep learning-based WSI analysis tasks spanning different tissue types. The results show that our framework generates explanations that accurately reflect the histomorphology underlying the model's predictions at both global and local levels. For interpretability and clinical utility in diagnostic contexts, human evaluation results showed that our explanations were easy to interpret, rich in diagnostic features, and directly helpful for diagnostic decision-making, thereby enhancing pathologist-AI collaboration. Our work highlights that unifying global and local explanations and grounding them in expert-interpreted morphology enhances the interpretability and verifiability of deep learning models, thereby facilitating the transparent deployment of such models in clinical practice.

Identifiers

PMID42135447
PMCPMC13408912

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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.