Evidence map›Paper›PMID 42794970›Full record

ArticleCancers2026

An Iterative, Pathologist-in-the-Loop Workflow for Generation of Clinical-Grade Synthetic Pathology Images in a Diverse Cohort of Pancreatic Tumors.

Yixi Xu, Md Nasir, Valentina Matos-Romero, Tiane Chen, Ralph H Hruban, William B Weeks, Rahul Dodhia, Juan Lavista Ferres, Ashley L Kiemen

Abstract read
In one paragraph

Article in Cancers, 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

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.

Yixi XuAI for Good Lab, Microsoft, Redmond, WA 98052, USA.
Md NasirAI for Good Lab, Microsoft, Redmond, WA 98052, USA.ORCID 0000-0002-3955-0996
Valentina Matos-RomeroDepartment of Chemical & Biomolecular Engineering, Johns Hopkins University, Baltimore, MD 21218, USA.
Tiane ChenThe Sol Goldman Pancreatic Cancer Research Center, Department of Pathology, Johns Hopkins University, Baltimore, MD 21218, USA.ORCID 0000-0003-4799-7488
Ralph H HrubanThe Sol Goldman Pancreatic Cancer Research Center, Department of Pathology, Johns Hopkins University, Baltimore, MD 21218, USA.ORCID 0000-0003-4554-5672
William B WeeksAI for Good Lab, Microsoft, Redmond, WA 98052, USA.
Rahul DodhiaAI for Good Lab, Microsoft, Redmond, WA 98052, USA.
Juan Lavista FerresAI for Good Lab, Microsoft, Redmond, WA 98052, USA.
Ashley L KiemenDepartment of Chemical & Biomolecular Engineering, Johns Hopkins University, Baltimore, MD 21218, USA.

Funding

Tech Core 2U54CA268083 · NCI · JOHNS HOPKINS UNIVERSITY · PI Denis Wirtz, Laura DeLong Wood · 2022 to 2026
$10.2M
Doug and Julie OstroverFCSP FoundationLustgarten Foundation-AACR Career Development Award for Pancreatic Cancer Research, in Honor of Ruth Bader GinsburgNCI NIH HHS U54 CA268083NCI NIH HHS U54CA268083Rolfe Pancreatic Cancer FoundationSusan Wojcicki and Denis TroperThe Carl and Carol Nale Fund for Pancreatic Cancer ResearchThe Joseph C. Monastra Foundation for Pancreatic Cancer ResearchThe Stringer Foundation
6 · The paper itself

Abstract

BACKGROUND/

objectivesThe training of diagnostic pancreatic pathologists is largely limited by the diversity of available pathology images, especially those of rare diseases or conditions.

methodsUsing a cohort of seven pancreatic neoplasms, we developed an iterative, pathologist-in-the-loop workflow integrating scalable tile pruning, generative-model optimization, and postprocessing truncation. Two pathologists evaluated synthetic-image quality and subtype representation on a 0-3 scale; the independent pathologist was blinded to image source and truncation condition and also rated curated real training tiles.

resultsUntruncated images had lower class-balanced FID than per-class-truncated images (6.64 versus 29.08) and higher recall and coverage, whereas truncation increased precision. The independent pathologist rated per-class-truncated images higher than matched non-truncated images (mean difference 0.80, bootstrap 95% CI 0.57-1.03). Quadratic-weighted Cohen's κ was 0.599 (95% CI 0.489-0.691); after grouping ratings as 0-1 versus 2-3, raw agreement was 80.7% (95% CI 75.0-86.4%).

conclusionsPer-class truncation improved independently rated image quality and subtype representation. Successful synthetic histology generation requires careful data curation, domain-specific oversight, and independent validation; clinical utility requires separate task-based evaluation.

Indexed as

artificial intelligencecomputational pathologyimage tilingpancreatic pathologysynthetic image generation

Identifiers

PMID42794970
PMCPMC13605902

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.