Toward comprehensive cellular characterization of H&E slides

Q2 Medicine
Journal of Pathology Informatics Pub Date : 2026-08-01 Epub Date: 2026-07-23 DOI:10.1016/j.jpi.2026.100696
Benjamin Adjadj, Pierre-Antoine Bannier, Guillaume Horent, Sebastien Mandela, Gary Klajer, Aurore Lyon, Kathryn Schutte, Ulysse Marteau, Valentin Gaury, Laura Dumont, Thomas Mathieu, Reda Belbahri, Benoît Schmauch, Eric Durand, Katharina Von Loga, Lucie Gillet
{"title":"Toward comprehensive cellular characterization of H&E slides","authors":"Benjamin Adjadj,&nbsp;Pierre-Antoine Bannier,&nbsp;Guillaume Horent,&nbsp;Sebastien Mandela,&nbsp;Gary Klajer,&nbsp;Aurore Lyon,&nbsp;Kathryn Schutte,&nbsp;Ulysse Marteau,&nbsp;Valentin Gaury,&nbsp;Laura Dumont,&nbsp;Thomas Mathieu,&nbsp;Reda Belbahri,&nbsp;Benoît Schmauch,&nbsp;Eric Durand,&nbsp;Katharina Von Loga,&nbsp;Lucie Gillet","doi":"10.1016/j.jpi.2026.100696","DOIUrl":null,"url":null,"abstract":"<div><div>Cell detection, segmentation, and classification are essential for analyzing tumor microenvironments (TME) on hematoxylin and eosin (H&amp;E) slides. Existing methods suffer from poor performance on understudied cell types (rare or not present in public datasets) and limited cross-domain generalization. To address these shortcomings, we introduce HistoPLUS, a state-of-the-art model for cell analysis, trained on a novel curated pan-cancer dataset of 108,722 nuclei covering 13 cell types. In external validation across 4 independent cohorts, HistoPLUS outperforms current state-of-the-art models in detection quality by 5.2% and overall F1 classification score by 23.7%, while using 5× fewer parameters. In addition, we show that HistoPLUS robustly transfers to two oncology indications unseen during training and allows interpretable biomarker discovery in downstream tasks, outperforming clinical baselines and prior deep learning methods. To support broader TME biomarker research, we release the model weights and inference code.</div></div>","PeriodicalId":37769,"journal":{"name":"Journal of Pathology Informatics","volume":"22 ","pages":"Article 100696"},"PeriodicalIF":0.0000,"publicationDate":"2026-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Pathology Informatics","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2153353926001562","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/7/23 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0

Abstract

Cell detection, segmentation, and classification are essential for analyzing tumor microenvironments (TME) on hematoxylin and eosin (H&E) slides. Existing methods suffer from poor performance on understudied cell types (rare or not present in public datasets) and limited cross-domain generalization. To address these shortcomings, we introduce HistoPLUS, a state-of-the-art model for cell analysis, trained on a novel curated pan-cancer dataset of 108,722 nuclei covering 13 cell types. In external validation across 4 independent cohorts, HistoPLUS outperforms current state-of-the-art models in detection quality by 5.2% and overall F1 classification score by 23.7%, while using 5× fewer parameters. In addition, we show that HistoPLUS robustly transfers to two oncology indications unseen during training and allows interpretable biomarker discovery in downstream tasks, outperforming clinical baselines and prior deep learning methods. To support broader TME biomarker research, we release the model weights and inference code.
对H&E玻片的全面细胞表征
细胞检测、分割和分类对于分析苏木精和伊红(H&;E)载玻片上的肿瘤微环境(TME)至关重要。现有的方法在未充分研究的细胞类型(在公共数据集中很少或不存在)上表现不佳,并且跨域泛化有限。为了解决这些缺点,我们引入了HistoPLUS,这是一种最先进的细胞分析模型,该模型是在一个涵盖13种细胞类型的108,722个细胞核的新型泛癌症数据集上训练的。在4个独立队列的外部验证中,HistoPLUS在检测质量上比目前最先进的模型高出5.2%,在F1分类总分上高出23.7%,同时使用的参数减少了5倍。此外,我们发现HistoPLUS稳健地转移到训练过程中未见的两种肿瘤适应症,并允许在下游任务中发现可解释的生物标志物,优于临床基线和先前的深度学习方法。为了支持更广泛的TME生物标志物研究,我们发布了模型权重和推理代码。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Journal of Pathology Informatics
Journal of Pathology Informatics Medicine-Pathology and Forensic Medicine
CiteScore
3.70
自引率
0.00%
发文量
2
审稿时长
18 weeks
期刊介绍: The Journal of Pathology Informatics (JPI) is an open access peer-reviewed journal dedicated to the advancement of pathology informatics. This is the official journal of the Association for Pathology Informatics (API). The journal aims to publish broadly about pathology informatics and freely disseminate all articles worldwide. This journal is of interest to pathologists, informaticians, academics, researchers, health IT specialists, information officers, IT staff, vendors, and anyone with an interest in informatics. We encourage submissions from anyone with an interest in the field of pathology informatics. We publish all types of papers related to pathology informatics including original research articles, technical notes, reviews, viewpoints, commentaries, editorials, symposia, meeting abstracts, book reviews, and correspondence to the editors. All submissions are subject to rigorous peer review by the well-regarded editorial board and by expert referees in appropriate specialties.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书