首页 > 最新文献

Journal of Pathology Informatics最新文献

英文 中文
Mathematical modelling and deep learning algorithms to automate assessment of single and digitally multiplexed immunohistochemical stains in tumoural stroma 用数学建模和深度学习算法自动评估肿瘤基质中的单一和数字多重免疫组化染色结果
Q2 Medicine Pub Date : 2023-11-19 DOI: 10.1016/j.jpi.2023.100351
Liam Burrows , Declan Sculthorpe , Hongrun Zhang , Obaid Rehman , Abhik Mukherjee , Ke Chen

Whilst automated analysis of immunostains in pathology research has focused predominantly on the epithelial compartment, automated analysis of stains in the stromal compartment is challenging and therefore requires time-consuming pathological input and guidance to adjust to tissue morphometry as perceived by pathologists. This study aimed to develop a robust method to automate stromal stain analyses using 2 of the commonest stromal stains (SMA and desmin) employed in clinical pathology practice as examples. An effective computational method capable of automatically assessing and quantifying tumour-associated stromal stains was developed and applied on cores of colorectal cancer tissue microarrays. The methodology combines both mathematical models and deep learning techniques with the former requiring no training data and the latter as many inputs as possible. The novel mathematical model was used to produce a digital double marker overlay allowing for fast automated digital multiplex analysis of stromal stains. The results show that deep learning methodologies in combination with mathematical modelling allow for an accurate means of quantifying stromal stains whilst also opening up new possibilities of digital multiplex analyses.

虽然病理学研究中免疫染色的自动分析主要集中在上皮室,但间质室染色的自动分析具有挑战性,因此需要耗时的病理输入和指导,以适应病理学家所感知的组织形态测定。本研究旨在以临床病理实践中常用的两种基质染色(SMA和desmin)为例,开发一种强大的方法来自动进行基质染色分析。开发了一种有效的计算方法,能够自动评估和量化肿瘤相关基质染色,并应用于结直肠癌组织微阵列核心。该方法结合了数学模型和深度学习技术,前者不需要训练数据,后者需要尽可能多的输入。新的数学模型被用来产生一个数字双标记覆盖,允许快速自动数字复用分析基质污渍。结果表明,深度学习方法与数学建模相结合,可以准确地量化基质染色,同时也为数字多路分析开辟了新的可能性。
{"title":"Mathematical modelling and deep learning algorithms to automate assessment of single and digitally multiplexed immunohistochemical stains in tumoural stroma","authors":"Liam Burrows ,&nbsp;Declan Sculthorpe ,&nbsp;Hongrun Zhang ,&nbsp;Obaid Rehman ,&nbsp;Abhik Mukherjee ,&nbsp;Ke Chen","doi":"10.1016/j.jpi.2023.100351","DOIUrl":"https://doi.org/10.1016/j.jpi.2023.100351","url":null,"abstract":"<div><p>Whilst automated analysis of immunostains in pathology research has focused predominantly on the epithelial compartment, automated analysis of stains in the stromal compartment is challenging and therefore requires time-consuming pathological input and guidance to adjust to tissue morphometry as perceived by pathologists. This study aimed to develop a robust method to automate stromal stain analyses using 2 of the commonest stromal stains (SMA and desmin) employed in clinical pathology practice as examples. An effective computational method capable of automatically assessing and quantifying tumour-associated stromal stains was developed and applied on cores of colorectal cancer tissue microarrays. The methodology combines both mathematical models and deep learning techniques with the former requiring no training data and the latter as many inputs as possible. The novel mathematical model was used to produce a digital double marker overlay allowing for fast automated digital multiplex analysis of stromal stains. The results show that deep learning methodologies in combination with mathematical modelling allow for an accurate means of quantifying stromal stains whilst also opening up new possibilities of digital multiplex analyses.</p></div>","PeriodicalId":37769,"journal":{"name":"Journal of Pathology Informatics","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2023-11-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2153353923001657/pdfft?md5=482b41c3d6029ab0f2c8de25168258df&pid=1-s2.0-S2153353923001657-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138633482","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Whole slide images as non-fungible tokens: A decentralized approach to secure, scalable data storage and access 作为不可篡改代币的整张幻灯片图像:安全、可扩展数据存储和访问的去中心化方法
Q2 Medicine Pub Date : 2023-11-09 DOI: 10.1016/j.jpi.2023.100350
Arlen Brickman , Yigit Baykara , Miguel Carabaño , Sean M. Hacking

Background

Distributed ledger technology (DLT) enables the creation of tamper-resistant, decentralized, and secure digital ledgers. A non-fungible token (NFT) represents a record on-chain associated with a digital or physical asset, such as a whole-slide image (WSI). The InterPlanetary File System (IPFS) represents an off-chain network, hypermedia, and file sharing peer-to-peer protocol for storing and sharing data in a distributed file system. Today, we need cheaper, more efficient, highly scalable, and transparent solutions for WSI data storage and access of medical records and medical imaging data.

Methods

WSIs were created from non-human tissues and H&E-stained sections were scanned on a Philips Ultrafast WSI scanner at 40× magnification objective lens (1 μm/pixel). TIFF images were stored on IPFS, while NFTs were minted on the Ethereum blockchain network in ERC-1155 standard. WSI-NFTs were stored on MetaMask and OpenSea was used to display the WSI-NFT collection. Filebase storage application programing interface (API) were used to create dedicated gateways and content delivery networks (CDN).

Results

A total of 10 WSI-NFTs were minted on the Ethereum blockchain network, found on our collection “Whole Slide Images as Non-fungible Tokens Project” on Open Sea: https://opensea.io/collection/untitled-collection-126765644. WSI TIFF files ranged in size from 1.6 to 2.2 GB and were stored on IPFS and pinned on 3 separate nodes. Under optimal conditions, and using a dedicated CDN, WSI reached retrieved at speeds of over 10 mb/s, however, download speeds and WSI retrieval times varied significantly depending on the file and gateway used. Overall, the public IPFS gateway resulted in variably poorer WSI download retrieval performance compared to gateways provided by Filebase storage API.

Conclusion

Whole-slide images, as the most complex and substantial data files in healthcare, demand innovative solutions. In this technical report, we identify pitfalls in IPFS, and demonstrate proof-of-concept using a 3-layer architecture for scalable, decentralized storage, and access. Optimized through dedicated gateways and CDNs, which can be effectively applied to all medical data and imaging modalities across the healthcare sector. DLT and off-chain network solutions present numerous opportunities for advancements in clinical care, education, and research. Such approaches uphold the principles of equitable healthcare data ownership, security, and democratization, and are poised to drive significant innovation.

背景分布式账本技术(DLT)能够创建防篡改、去中心化和安全的数字账本。不可篡改令牌(NFT)代表与数字或物理资产(如整张幻灯片图像(WSI))相关的链上记录。星际文件系统(IPFS)是一种链外网络、超媒体和文件共享点对点协议,用于在分布式文件系统中存储和共享数据。如今,我们需要更便宜、更高效、可高度扩展和透明的解决方案来存储 WSI 数据,并访问医疗记录和医学成像数据。方法从非人类组织创建 WSI,并在飞利浦超快 WSI 扫描仪上以 40 倍放大率物镜(1 微米/像素)扫描 H&E 染色切片。TIFF 图像存储在 IPFS 上,而 NFT 则以 ERC-1155 标准在以太坊区块链网络上铸造。WSI-NFT存储在MetaMask上,OpenSea用于显示WSI-NFT集合。Filebase 存储应用编程接口(API)被用于创建专用网关和内容交付网络(CDN)。结果在以太坊区块链网络上总共铸造了 10 个 WSI-NFT,这些 WSI-NFT 在 Open Sea 上的 "整张幻灯片图像作为不可篡改代币项目 "集合中找到:https://opensea.io/collection/untitled-collection-126765644。WSI TIFF 文件的大小从 1.6 GB 到 2.2 GB 不等,存储在 IPFS 上,并固定在 3 个不同的节点上。在最佳条件下,使用专门的 CDN,WSI 的检索速度超过 10 mb/s,但下载速度和 WSI 检索时间因文件和使用的网关不同而有很大差异。总体而言,与 Filebase 存储 API 提供的网关相比,公共 IPFS 网关的 WSI 下载检索性能要差一些。在本技术报告中,我们指出了 IPFS 中存在的缺陷,并使用可扩展、分散存储和访问的 3 层架构演示了概念验证。通过专用网关和 CDN 进行优化,可有效应用于医疗保健领域的所有医疗数据和成像模式。DLT 和链外网络解决方案为临床护理、教育和研究的进步提供了大量机会。这些方法坚持公平的医疗数据所有权、安全性和民主化原则,有望推动重大创新。
{"title":"Whole slide images as non-fungible tokens: A decentralized approach to secure, scalable data storage and access","authors":"Arlen Brickman ,&nbsp;Yigit Baykara ,&nbsp;Miguel Carabaño ,&nbsp;Sean M. Hacking","doi":"10.1016/j.jpi.2023.100350","DOIUrl":"10.1016/j.jpi.2023.100350","url":null,"abstract":"<div><h3>Background</h3><p>Distributed ledger technology (DLT) enables the creation of tamper-resistant, decentralized, and secure digital ledgers. A non-fungible token (NFT) represents a record on-chain associated with a digital or physical asset, such as a whole-slide image (WSI). The InterPlanetary File System (IPFS) represents an off-chain network, hypermedia, and file sharing peer-to-peer protocol for storing and sharing data in a distributed file system. Today, we need cheaper, more efficient, highly scalable, and transparent solutions for WSI data storage and access of medical records and medical imaging data.</p></div><div><h3>Methods</h3><p>WSIs were created from non-human tissues and H&amp;E-stained sections were scanned on a Philips Ultrafast WSI scanner at 40× magnification objective lens (1 μm/pixel). TIFF images were stored on IPFS, while NFTs were minted on the Ethereum blockchain network in ERC-1155 standard. WSI-NFTs were stored on MetaMask and OpenSea was used to display the WSI-NFT collection. Filebase storage application programing interface (API) were used to create dedicated gateways and content delivery networks (CDN).</p></div><div><h3>Results</h3><p>A total of 10 WSI-NFTs were minted on the Ethereum blockchain network, found on our collection “Whole Slide Images as Non-fungible Tokens Project” on Open Sea: <span>https://opensea.io/collection/untitled-collection-126765644</span><svg><path></path></svg>. WSI TIFF files ranged in size from 1.6 to 2.2 GB and were stored on IPFS and pinned on 3 separate nodes. Under optimal conditions, and using a dedicated CDN, WSI reached retrieved at speeds of over 10 mb/s, however, download speeds and WSI retrieval times varied significantly depending on the file and gateway used. Overall, the public IPFS gateway resulted in variably poorer WSI download retrieval performance compared to gateways provided by Filebase storage API.</p></div><div><h3>Conclusion</h3><p>Whole-slide images, as the most complex and substantial data files in healthcare, demand innovative solutions. In this technical report, we identify pitfalls in IPFS, and demonstrate proof-of-concept using a 3-layer architecture for scalable, decentralized storage, and access. Optimized through dedicated gateways and CDNs, which can be effectively applied to all medical data and imaging modalities across the healthcare sector. DLT and off-chain network solutions present numerous opportunities for advancements in clinical care, education, and research. Such approaches uphold the principles of equitable healthcare data ownership, security, and democratization, and are poised to drive significant innovation.</p></div>","PeriodicalId":37769,"journal":{"name":"Journal of Pathology Informatics","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2023-11-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2153353923001645/pdfft?md5=4164e105de7f34e0cc4b4035d1797cb6&pid=1-s2.0-S2153353923001645-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135565552","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Cognitive factors impacting patient understanding of laboratory test information 认知因素影响患者对实验室检测信息的理解
Q2 Medicine Pub Date : 2023-11-08 DOI: 10.1016/j.jpi.2023.100349
Edward C. Klatt

Laboratory testing can provide information useful to promote patient health literacy and ultimately patient well-being. The human state of mind involves not only cognition but also emotion and motivation factors when receiving, processing, and acting upon information. The cognitive load for patients acquiring and processing new information is high. Modes of distribution can affect both attention to and receipt of information. Implicit unconscious biases can affect whom and what patients believe. Positive wording and framing of information with salience for patients can evoke positive emotions. Providing patients with the gist, or essential meaning, of information can positively influence decision-making. What laboratorians provide as information helps to combat mis- and disinformation. Laboratorians can actively participate in measures to improve the patient experience in health care by developing and contributing to high-quality information to enable timely, meaningful communication and interpretation of test results.

实验室检测可以提供有用的信息,以促进患者健康知识,并最终提高患者的福祉。人的心理状态不仅包括认知,还包括接收、处理和对信息采取行动时的情感和动机因素。患者获取和处理新信息的认知负荷较高。传播方式会影响对信息的关注和接收。内隐的无意识偏见会影响患者的信仰。积极的措辞和信息框架对患者具有显著性,可以唤起积极情绪。向患者提供信息的要点或基本含义可以对决策产生积极影响。实验室提供的信息有助于打击错误和虚假信息。通过开发和提供高质量信息,以便及时、有意义地沟通和解释检测结果,实验室人员可以积极参与改善患者在医疗保健中的体验的措施。
{"title":"Cognitive factors impacting patient understanding of laboratory test information","authors":"Edward C. Klatt","doi":"10.1016/j.jpi.2023.100349","DOIUrl":"10.1016/j.jpi.2023.100349","url":null,"abstract":"<div><p>Laboratory testing can provide information useful to promote patient health literacy and ultimately patient well-being. The human state of mind involves not only cognition but also emotion and motivation factors when receiving, processing, and acting upon information. The cognitive load for patients acquiring and processing new information is high. Modes of distribution can affect both attention to and receipt of information. Implicit unconscious biases can affect whom and what patients believe. Positive wording and framing of information with salience for patients can evoke positive emotions. Providing patients with the gist, or essential meaning, of information can positively influence decision-making. What laboratorians provide as information helps to combat mis- and disinformation. Laboratorians can actively participate in measures to improve the patient experience in health care by developing and contributing to high-quality information to enable timely, meaningful communication and interpretation of test results.</p></div>","PeriodicalId":37769,"journal":{"name":"Journal of Pathology Informatics","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2023-11-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2153353923001633/pdfft?md5=00b861355861322a8aaa479615ff15fe&pid=1-s2.0-S2153353923001633-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135515811","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Performance of externally validated machine learning models based on histopathology images for the diagnosis, classification, prognosis, or treatment outcome prediction in female breast cancer: A systematic review 基于组织病理学图像的外部验证机器学习模型在女性乳腺癌诊断、分类、预后或治疗效果预测方面的表现:系统综述
Q2 Medicine Pub Date : 2023-11-05 DOI: 10.1016/j.jpi.2023.100348
Ricardo Gonzalez , Peyman Nejat , Ashirbani Saha , Clinton J.V. Campbell , Andrew P. Norgan , Cynthia Lokker

Numerous machine learning (ML) models have been developed for breast cancer using various types of data. Successful external validation (EV) of ML models is important evidence of their generalizability. The aim of this systematic review was to assess the performance of externally validated ML models based on histopathology images for diagnosis, classification, prognosis, or treatment outcome prediction in female breast cancer. A systematic search of MEDLINE, EMBASE, CINAHL, IEEE, MICCAI, and SPIE conferences was performed for studies published between January 2010 and February 2022. The Prediction Model Risk of Bias Assessment Tool (PROBAST) was employed, and the results were narratively described. Of the 2011 non-duplicated citations, 8 journal articles and 2 conference proceedings met inclusion criteria. Three studies externally validated ML models for diagnosis, 4 for classification, 2 for prognosis, and 1 for both classification and prognosis. Most studies used Convolutional Neural Networks and one used logistic regression algorithms. For diagnostic/classification models, the most common performance metrics reported in the EV were accuracy and area under the curve, which were greater than 87% and 90%, respectively, using pathologists' annotations/diagnoses as ground truth. The hazard ratios in the EV of prognostic ML models were between 1.7 (95% CI, 1.2–2.6) and 1.8 (95% CI, 1.3–2.7) to predict distant disease-free survival; 1.91 (95% CI, 1.11–3.29) for recurrence, and between 0.09 (95% CI, 0.01–0.70) and 0.65 (95% CI, 0.43–0.98) for overall survival, using clinical data as ground truth. Despite EV being an important step before the clinical application of a ML model, it hasn't been performed routinely. The large variability in the training/validation datasets, methods, performance metrics, and reported information limited the comparison of the models and the analysis of their results. Increasing the availability of validation datasets and implementing standardized methods and reporting protocols may facilitate future analyses.

利用各种类型的数据为乳腺癌开发了大量机器学习(ML)模型。ML 模型成功的外部验证(EV)是其通用性的重要证据。本系统综述旨在评估经过外部验证的基于组织病理学图像的机器学习模型在女性乳腺癌诊断、分类、预后或治疗效果预测方面的性能。我们对 2010 年 1 月至 2022 年 2 月期间发表的研究进行了系统检索,包括 MEDLINE、EMBASE、CINAHL、IEEE、MICCAI 和 SPIE 会议。采用了预测模型偏倚风险评估工具(PROBAST),并对结果进行了叙述性描述。在 2011 年的非重复引用中,有 8 篇期刊论文和 2 篇会议论文集符合纳入标准。3 项研究对用于诊断的 ML 模型进行了外部验证,4 项用于分类,2 项用于预后,1 项用于分类和预后。大多数研究使用了卷积神经网络,一项研究使用了逻辑回归算法。对于诊断/分类模型,EV 报告中最常见的性能指标是准确率和曲线下面积,以病理学家的注释/诊断为基本事实,准确率和曲线下面积分别大于 87% 和 90%。使用临床数据作为基本真相,预后 ML 模型 EV 中预测远期无病生存的危险比介于 1.7(95% CI,1.2-2.6)和 1.8(95% CI,1.3-2.7)之间;预测复发的危险比介于 1.91(95% CI,1.11-3.29)之间;预测总生存的危险比介于 0.09(95% CI,0.01-0.70)和 0.65(95% CI,0.43-0.98)之间。尽管EV是ML模型临床应用前的一个重要步骤,但它还没有被常规化。训练/验证数据集、方法、性能指标和报告信息的巨大差异限制了模型的比较和结果分析。增加验证数据集的可用性并实施标准化的方法和报告协议可能会促进未来的分析。
{"title":"Performance of externally validated machine learning models based on histopathology images for the diagnosis, classification, prognosis, or treatment outcome prediction in female breast cancer: A systematic review","authors":"Ricardo Gonzalez ,&nbsp;Peyman Nejat ,&nbsp;Ashirbani Saha ,&nbsp;Clinton J.V. Campbell ,&nbsp;Andrew P. Norgan ,&nbsp;Cynthia Lokker","doi":"10.1016/j.jpi.2023.100348","DOIUrl":"10.1016/j.jpi.2023.100348","url":null,"abstract":"<div><p>Numerous machine learning (ML) models have been developed for breast cancer using various types of data. Successful external validation (EV) of ML models is important evidence of their generalizability. The aim of this systematic review was to assess the performance of externally validated ML models based on histopathology images for diagnosis, classification, prognosis, or treatment outcome prediction in female breast cancer. A systematic search of MEDLINE, EMBASE, CINAHL, IEEE, MICCAI, and SPIE conferences was performed for studies published between January 2010 and February 2022. The Prediction Model Risk of Bias Assessment Tool (PROBAST) was employed, and the results were narratively described. Of the 2011 non-duplicated citations, 8 journal articles and 2 conference proceedings met inclusion criteria. Three studies externally validated ML models for diagnosis, 4 for classification, 2 for prognosis, and 1 for both classification and prognosis. Most studies used Convolutional Neural Networks and one used logistic regression algorithms. For diagnostic/classification models, the most common performance metrics reported in the EV were accuracy and area under the curve, which were greater than 87% and 90%, respectively, using pathologists' annotations/diagnoses as ground truth. The hazard ratios in the EV of prognostic ML models were between 1.7 (95% CI, 1.2–2.6) and 1.8 (95% CI, 1.3–2.7) to predict distant disease-free survival; 1.91 (95% CI, 1.11–3.29) for recurrence, and between 0.09 (95% CI, 0.01–0.70) and 0.65 (95% CI, 0.43–0.98) for overall survival, using clinical data as ground truth. Despite EV being an important step before the clinical application of a ML model, it hasn't been performed routinely. The large variability in the training/validation datasets, methods, performance metrics, and reported information limited the comparison of the models and the analysis of their results. Increasing the availability of validation datasets and implementing standardized methods and reporting protocols may facilitate future analyses.</p></div>","PeriodicalId":37769,"journal":{"name":"Journal of Pathology Informatics","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2023-11-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2153353923001621/pdfft?md5=065ed1f82e40c99cefb1eb56d5945b9c&pid=1-s2.0-S2153353923001621-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135455650","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
AI-based digital histopathology for perihilar cholangiocarcinoma: A step, not a jump 基于人工智能的肝门周围胆管癌数字组织病理学:一个步骤,而不是一个跳跃
Q2 Medicine Pub Date : 2023-11-05 DOI: 10.1016/j.jpi.2023.100345
Dieter P. Hoyer , Saskia Ting , Nina Rogacka , Sven Koitka , René Hosch , Nils Flaschel , Johannes Haubold , Eugen Malamutmann , Björn-Ole Stüben , Jürgen Treckmann , Felix Nensa , Giulia Baldini

Introduction

Perihilar cholangiocarcinoma (PHCC) is a rare malignancy with limited survival prediction accuracy. Artificial intelligence (AI) and digital pathology advancements have shown promise in predicting outcomes in cancer. We aimed to improve prognosis prediction for PHCC by combining AI-based histopathological slide analysis with clinical factors.

Methods

We retrospectively analyzed 317 surgically treated PHCC patients (January 2009–December 2018) at the University Hospital of Essen. Clinical data, surgical details, pathology, and outcomes were collected. Convolutional neural networks (CNN) analyzed whole-slide images. Survival models incorporated clinical and histological features.

Results

Among 142 eligible patients, independent survival predictors were tumor grade (G), tumor size (T), and intraoperative transfusion requirement. The CNN-based model combining clinical and histopathological features demonstrates proof of concept in prognosis prediction, limited by histopathological complexity and feature extraction challenges. However, the CNN-based model generated heatmaps assisting pathologists in identifying areas of interest.

Conclusion

AI-based digital pathology showed potential in PHCC prognosis prediction, though refinement is necessary for clinical relevance. Future research should focus on enhancing AI models and exploring novel approaches to improve PHCC patient prognosis prediction.

肝门周围胆管癌(PHCC)是一种罕见的恶性肿瘤,其生存预测精度有限。人工智能(AI)和数字病理学的进步在预测癌症结果方面显示出了希望。我们的目的是将基于人工智能的组织病理切片分析与临床因素相结合,提高PHCC的预后预测。方法回顾性分析2009年1月至2018年12月在埃森大学医院接受手术治疗的317例PHCC患者。收集临床资料、手术细节、病理和结果。卷积神经网络(CNN)分析了整个幻灯片图像。生存模型结合了临床和组织学特征。结果在142例符合条件的患者中,独立生存预测因子为肿瘤分级(G)、肿瘤大小(T)和术中输血需求。结合临床和组织病理学特征的基于cnn的模型在预测预后方面证明了概念的正确性,但受到组织病理学复杂性和特征提取挑战的限制。然而,基于cnn的模型生成了热图,帮助病理学家识别感兴趣的区域。结论人工智能数字病理在PHCC预后预测中具有一定的应用价值,但仍需进一步完善。未来的研究应注重增强人工智能模型,探索改善PHCC患者预后预测的新方法。
{"title":"AI-based digital histopathology for perihilar cholangiocarcinoma: A step, not a jump","authors":"Dieter P. Hoyer ,&nbsp;Saskia Ting ,&nbsp;Nina Rogacka ,&nbsp;Sven Koitka ,&nbsp;René Hosch ,&nbsp;Nils Flaschel ,&nbsp;Johannes Haubold ,&nbsp;Eugen Malamutmann ,&nbsp;Björn-Ole Stüben ,&nbsp;Jürgen Treckmann ,&nbsp;Felix Nensa ,&nbsp;Giulia Baldini","doi":"10.1016/j.jpi.2023.100345","DOIUrl":"10.1016/j.jpi.2023.100345","url":null,"abstract":"<div><h3>Introduction</h3><p>Perihilar cholangiocarcinoma (PHCC) is a rare malignancy with limited survival prediction accuracy. Artificial intelligence (AI) and digital pathology advancements have shown promise in predicting outcomes in cancer. We aimed to improve prognosis prediction for PHCC by combining AI-based histopathological slide analysis with clinical factors.</p></div><div><h3>Methods</h3><p>We retrospectively analyzed 317 surgically treated PHCC patients (January 2009–December 2018) at the University Hospital of Essen. Clinical data, surgical details, pathology, and outcomes were collected. Convolutional neural networks (CNN) analyzed whole-slide images. Survival models incorporated clinical and histological features.</p></div><div><h3>Results</h3><p>Among 142 eligible patients, independent survival predictors were tumor grade (G), tumor size (T), and intraoperative transfusion requirement. The CNN-based model combining clinical and histopathological features demonstrates proof of concept in prognosis prediction, limited by histopathological complexity and feature extraction challenges. However, the CNN-based model generated heatmaps assisting pathologists in identifying areas of interest.</p></div><div><h3>Conclusion</h3><p>AI-based digital pathology showed potential in PHCC prognosis prediction, though refinement is necessary for clinical relevance. Future research should focus on enhancing AI models and exploring novel approaches to improve PHCC patient prognosis prediction.</p></div>","PeriodicalId":37769,"journal":{"name":"Journal of Pathology Informatics","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2023-11-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2153353923001591/pdfft?md5=6306a1e73353f828e6b03fecfd67c6cf&pid=1-s2.0-S2153353923001591-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135455655","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Seeing the random forest through the decision trees. Supporting learning health systems from histopathology with machine learning models: Challenges and opportunities 通过决策树来观察随机森林。用机器学习模型支持组织病理学学习卫生系统:挑战与机遇
Q2 Medicine Pub Date : 2023-11-04 DOI: 10.1016/j.jpi.2023.100347
Ricardo Gonzalez , Ashirbani Saha , Clinton J.V. Campbell , Peyman Nejat , Cynthia Lokker , Andrew P. Norgan

This paper discusses some overlooked challenges faced when working with machine learning models for histopathology and presents a novel opportunity to support “Learning Health Systems” with them. Initially, the authors elaborate on these challenges after separating them according to their mitigation strategies: those that need innovative approaches, time, or future technological capabilities and those that require a conceptual reappraisal from a critical perspective. Then, a novel opportunity to support "Learning Health Systems" by integrating hidden information extracted by ML models from digitalized histopathology slides with other healthcare big data is presented.

本文讨论了在使用组织病理学机器学习模型时面临的一些被忽视的挑战,并提出了一个新的机会来支持“学习健康系统”。最初,作者根据缓解策略将这些挑战区分开来,然后详细阐述了这些挑战:那些需要创新方法、时间或未来技术能力的挑战,以及那些需要从批判性角度重新评估概念的挑战。然后,通过将ML模型从数字化组织病理学幻灯片中提取的隐藏信息与其他医疗保健大数据相结合,提出了一种支持“学习健康系统”的新机会。
{"title":"Seeing the random forest through the decision trees. Supporting learning health systems from histopathology with machine learning models: Challenges and opportunities","authors":"Ricardo Gonzalez ,&nbsp;Ashirbani Saha ,&nbsp;Clinton J.V. Campbell ,&nbsp;Peyman Nejat ,&nbsp;Cynthia Lokker ,&nbsp;Andrew P. Norgan","doi":"10.1016/j.jpi.2023.100347","DOIUrl":"10.1016/j.jpi.2023.100347","url":null,"abstract":"<div><p>This paper discusses some overlooked challenges faced when working with machine learning models for histopathology and presents a novel opportunity to support “Learning Health Systems” with them. Initially, the authors elaborate on these challenges after separating them according to their mitigation strategies: those that need innovative approaches, time, or future technological capabilities and those that require a conceptual reappraisal from a critical perspective. Then, a novel opportunity to support \"Learning Health Systems\" by integrating hidden information extracted by ML models from digitalized histopathology slides with other healthcare big data is presented.</p></div>","PeriodicalId":37769,"journal":{"name":"Journal of Pathology Informatics","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2023-11-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S215335392300161X/pdfft?md5=61eb80bf2823facaa480b73e1391ad92&pid=1-s2.0-S215335392300161X-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135412417","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Computational pathology in the identification of HER2-low breast cancer: Opportunities and challenges 计算病理学在低her2乳腺癌鉴别中的应用:机遇与挑战
Q2 Medicine Pub Date : 2023-11-04 DOI: 10.1016/j.jpi.2023.100343
Marie Brevet , Zaibo Li , Anil Parwani

For the past 2 decades, pathologists have been accustomed to reporting the HER2 status of breast cancer as either positive or negative, based on HER2 IHC. Today, however, there is a clinical imperative to employ a 3-tier approach to interpreting HER2 IHC that can also identify tumours categorised as HER2-low. Meeting this need for a finer degree of discrimination may be challenging, and in this article, we consider the potential for the integration of computational approaches to support pathologists in achieving accurate and reproducible HER2 IHC scoring as well as outlining some of the practicalities involved.

在过去的20年里,病理学家已经习惯于根据HER2免疫组化报告乳腺癌的HER2状态为阳性或阴性。然而,如今临床迫切需要采用三层方法来解释HER2免疫组化,这种方法也可以识别归类为HER2低的肿瘤。满足这种对更精细程度的区分的需求可能具有挑战性,在本文中,我们考虑了整合计算方法的潜力,以支持病理学家实现准确和可重复的HER2 IHC评分,并概述了一些涉及的实用性。
{"title":"Computational pathology in the identification of HER2-low breast cancer: Opportunities and challenges","authors":"Marie Brevet ,&nbsp;Zaibo Li ,&nbsp;Anil Parwani","doi":"10.1016/j.jpi.2023.100343","DOIUrl":"10.1016/j.jpi.2023.100343","url":null,"abstract":"<div><p>For the past 2 decades, pathologists have been accustomed to reporting the HER2 status of breast cancer as either positive or negative, based on HER2 IHC. Today, however, there is a clinical imperative to employ a 3-tier approach to interpreting HER2 IHC that can also identify tumours categorised as HER2-low. Meeting this need for a finer degree of discrimination may be challenging, and in this article, we consider the potential for the integration of computational approaches to support pathologists in achieving accurate and reproducible HER2 IHC scoring as well as outlining some of the practicalities involved.</p></div>","PeriodicalId":37769,"journal":{"name":"Journal of Pathology Informatics","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2023-11-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2153353923001578/pdfft?md5=8fd6af9fd78e655c07d1b2afbe73f9a5&pid=1-s2.0-S2153353923001578-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135455777","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Comparative evaluation of slide scanners, scan settings, and cytopreparations for digital urine cytology 数字化尿液细胞学的滑动扫描仪、扫描设置和细胞修复的比较评价
Q2 Medicine Pub Date : 2023-11-04 DOI: 10.1016/j.jpi.2023.100346
Jen-Fan Hang , Yen-Chuan Ou , Wei-Lei Yang , Tang-Yi Tsao , Cheng-Hung Yeh , Chi-Bin Li , En-Yu Hsu , Po-Yen Hung , Yi-Ting Hwang , Tien-Jen Liu , Min-Che Tung

Background

Acquiring well-focused digital images of cytology slides with scanners can be challenging due to the 3-dimensional nature of the slides. This study evaluates performances of whole-slide images (WSIs) obtained from 2 different cytopreparations by 2 distinct scanners with 3 focus modes.

Methods

Fourteen urine specimens were collected from patients with urothelial carcinoma. Each specimen was equally divided into 2 portions, prepared with Cytospin and ThinPrep methods and scanned for WSIs using Leica (Aperio AT2) and Hamamatsu (NanoZoomer S360) scanners, respectively. The scan settings included 3 focus modes (default, semi-auto, and manual) for single-layer scanning, along with a manual focus mode for 21 Z-layers scanning. Performance metrics were evaluated including scanning success rate, artificial intelligence (AI) algorithm-inferred atypical cell numbers and coverage rate (atypical cell numbers in single or multiple Z-layers divided by the total atypical cell numbers in 21 Z-layers), scanning time, and image file size.

Results

The default mode had scanning success rates of 85.7% or 92.9%, depending on the scanner used. The semi-auto mode increased success to 92.9% or 100%, and manual even further to 100%. However, these changes did not affect the standardized median atypical cell numbers and coverage rates. The selection of scanners, cytopreparations, and Z-stacking influenced standardized median atypical cell numbers and coverage rates, scanning times, and image file sizes.

Discussion

Both scanners showed satisfactory scanning. We recommend using semi-auto or manual focus modes to achieve a scanning success rate of up to 100%. Additionally, a minimum of 9-layer Z-stacking at 1 μm intervals is required to cover 80% of atypical cells. These advanced focus methods do not impact the number of atypical cells or their coverage rate. While Z-stacking enhances the AI algorithm's inferred quantity and coverage rates of atypical cells, it simultaneously results in longer scanning times and larger image file sizes.

由于玻片的三维性质,用扫描仪获取聚焦良好的细胞学玻片数字图像可能具有挑战性。本研究评估了两种不同的扫描仪、三种聚焦模式下从两种不同的细胞修复中获得的全片图像(wsi)的性能。方法收集14例尿路上皮癌患者尿液标本。每个标本平均分成2份,分别用Cytospin和ThinPrep方法制备,分别用Leica (Aperio AT2)和Hamamatsu (NanoZoomer S360)扫描仪扫描wsi。扫描设置包括3种对焦模式(默认,半自动和手动),用于单层扫描,以及21 z层扫描的手动对焦模式。评估的性能指标包括扫描成功率、人工智能(AI)算法推断的非典型细胞数和覆盖率(单个或多个z层的非典型细胞数除以21个z层的非典型细胞总数)、扫描时间和图像文件大小。结果默认模式的扫描成功率分别为85.7%和92.9%,具体取决于所使用的扫描仪。半自动模式将成功率提高到92.9%或100%,手动模式甚至进一步提高到100%。然而,这些变化并不影响标准化中位数非典型细胞数和覆盖率。扫描仪的选择、细胞修复和z堆叠影响标准化中位数非典型细胞数和覆盖率、扫描时间和图像文件大小。两种扫描器显示满意的扫描。我们建议使用半自动或手动对焦模式来实现高达100%的扫描成功率。此外,至少需要以1 μm的间隔进行9层z堆叠,以覆盖80%的非典型细胞。这些先进的聚焦方法不影响非典型细胞的数量或它们的覆盖率。Z-stacking在增强AI算法推断非典型细胞数量和覆盖率的同时,导致扫描时间变长,图像文件大小变大。
{"title":"Comparative evaluation of slide scanners, scan settings, and cytopreparations for digital urine cytology","authors":"Jen-Fan Hang ,&nbsp;Yen-Chuan Ou ,&nbsp;Wei-Lei Yang ,&nbsp;Tang-Yi Tsao ,&nbsp;Cheng-Hung Yeh ,&nbsp;Chi-Bin Li ,&nbsp;En-Yu Hsu ,&nbsp;Po-Yen Hung ,&nbsp;Yi-Ting Hwang ,&nbsp;Tien-Jen Liu ,&nbsp;Min-Che Tung","doi":"10.1016/j.jpi.2023.100346","DOIUrl":"10.1016/j.jpi.2023.100346","url":null,"abstract":"<div><h3>Background</h3><p>Acquiring well-focused digital images of cytology slides with scanners can be challenging due to the 3-dimensional nature of the slides. This study evaluates performances of whole-slide images (WSIs) obtained from 2 different cytopreparations by 2 distinct scanners with 3 focus modes.</p></div><div><h3>Methods</h3><p>Fourteen urine specimens were collected from patients with urothelial carcinoma. Each specimen was equally divided into 2 portions, prepared with Cytospin and ThinPrep methods and scanned for WSIs using Leica (Aperio AT2) and Hamamatsu (NanoZoomer S360) scanners, respectively. The scan settings included 3 focus modes (default, semi-auto, and manual) for single-layer scanning, along with a manual focus mode for 21 Z-layers scanning. Performance metrics were evaluated including scanning success rate, artificial intelligence (AI) algorithm-inferred atypical cell numbers and coverage rate (atypical cell numbers in single or multiple Z-layers divided by the total atypical cell numbers in 21 Z-layers), scanning time, and image file size.</p></div><div><h3>Results</h3><p>The default mode had scanning success rates of 85.7% or 92.9%, depending on the scanner used. The semi-auto mode increased success to 92.9% or 100%, and manual even further to 100%. However, these changes did not affect the standardized median atypical cell numbers and coverage rates. The selection of scanners, cytopreparations, and Z-stacking influenced standardized median atypical cell numbers and coverage rates, scanning times, and image file sizes.</p></div><div><h3>Discussion</h3><p>Both scanners showed satisfactory scanning. We recommend using semi-auto or manual focus modes to achieve a scanning success rate of up to 100%. Additionally, a minimum of 9-layer Z-stacking at 1 μm intervals is required to cover 80% of atypical cells. These advanced focus methods do not impact the number of atypical cells or their coverage rate. While Z-stacking enhances the AI algorithm's inferred quantity and coverage rates of atypical cells, it simultaneously results in longer scanning times and larger image file sizes.</p></div>","PeriodicalId":37769,"journal":{"name":"Journal of Pathology Informatics","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2023-11-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2153353923001608/pdfft?md5=2ee536dfedd3c029d54d522a3a6fa784&pid=1-s2.0-S2153353923001608-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135455421","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Learning to predict prostate cancer recurrence from tissue images 学习从组织图像预测前列腺癌复发
Q2 Medicine Pub Date : 2023-11-01 DOI: 10.1016/j.jpi.2023.100344
Mahtab Farrokh, Neeraj Kumar, Peter H. Gann, Russell Greiner
Roughly 30% of men with prostate cancer who undergo radical prostatectomy will suffer biochemical cancer recurrence (BCR). Accurately predicting which patients will experience BCR could identify who would benefit from increased surveillance or adjuvant therapy. Unfortunately, no current method can effectively predict this. We develop and evaluate PathCLR, a novel semi-supervised method that learns a model that can use hematoxylin and eosin (H&E)-stained tissue microarrays (TMAs) to predict prostate cancer recurrence within 5 years after diagnosis. The learning process involves 2 sequential steps: PathCLR (a) first employs self-supervised learning to generate effective feature representations of the input images, then (b) feeds these learned features into a fully supervised neural network classifier to learn a model for predicting BCR. We conducted training and evaluation using 2 large prostate cancer datasets: (1) the Cooperative Prostate Cancer Tissue Resource (CPCTR) with 374 patients, including 189 who experienced BCR, and (2) the Johns Hopkins University (JHU) prostate cancer dataset of 646 patients, with 451 patients having BCR. PathCLR’s (10-fold cross-validation) F1 score was 0.61 for CPCTR and 0.85 for JHU. This was statistically superior (paired t-test with P<.05) to the best-learned model that relied solely on clinicopathological features, including PSA level, primary and secondary Gleason Grade, etc. We attribute the improvement of PathCLR over models using only clinicopathological features to its utilization of both learned latent representations of tissue core images and clinicopathological features. This finding suggests that there is essential predictive information in tissue images at the time of surgery that goes beyond the knowledge obtained from reported clinicopathological features, helping predict the patient’s 5-year outcome.
大约30%的前列腺癌患者接受根治性前列腺切除术后会出现生化癌复发(BCR)。准确预测哪些患者将经历BCR,可以确定哪些患者将受益于加强监测或辅助治疗。不幸的是,目前没有任何方法可以有效地预测这一点。我们开发并评估了PathCLR,这是一种新颖的半监督方法,可以学习一个模型,该模型可以使用苏木精和伊红(H&E)染色的组织微阵列(TMAs)来预测前列腺癌诊断后5年内的复发。学习过程包括两个连续的步骤:PathCLR (a)首先使用自监督学习来生成输入图像的有效特征表示,然后(b)将这些学习到的特征输入到一个完全监督的神经网络分类器中,以学习预测BCR的模型。我们使用两个大型前列腺癌数据集进行培训和评估:(1)合作前列腺癌组织资源(CPCTR)的374例患者,其中189例经历过BCR;(2)约翰霍普金斯大学(JHU)的646例患者的前列腺癌数据集,其中451例患有BCR。CPCTR的PathCLR(10倍交叉验证)F1评分为0.61,JHU为0.85。这在统计学上优于仅依赖临床病理特征(包括PSA水平、原发性和继发性Gleason分级等)的最佳学习模型(配对t检验P< 0.05)。我们将PathCLR优于仅使用临床病理特征的模型归因于其对组织核心图像和临床病理特征的习得潜在表征的利用。这一发现表明,在手术时的组织图像中有必要的预测信息,这些信息超出了从报告的临床病理特征中获得的知识,有助于预测患者的5年预后。
{"title":"Learning to predict prostate cancer recurrence from tissue images","authors":"Mahtab Farrokh, Neeraj Kumar, Peter H. Gann, Russell Greiner","doi":"10.1016/j.jpi.2023.100344","DOIUrl":"https://doi.org/10.1016/j.jpi.2023.100344","url":null,"abstract":"Roughly 30% of men with prostate cancer who undergo radical prostatectomy will suffer biochemical cancer recurrence (BCR). Accurately predicting which patients will experience BCR could identify who would benefit from increased surveillance or adjuvant therapy. Unfortunately, no current method can effectively predict this. We develop and evaluate PathCLR, a novel semi-supervised method that learns a model that can use hematoxylin and eosin (H&E)-stained tissue microarrays (TMAs) to predict prostate cancer recurrence within 5 years after diagnosis. The learning process involves 2 sequential steps: PathCLR (a) first employs self-supervised learning to generate effective feature representations of the input images, then (b) feeds these learned features into a fully supervised neural network classifier to learn a model for predicting BCR. We conducted training and evaluation using 2 large prostate cancer datasets: (1) the Cooperative Prostate Cancer Tissue Resource (CPCTR) with 374 patients, including 189 who experienced BCR, and (2) the Johns Hopkins University (JHU) prostate cancer dataset of 646 patients, with 451 patients having BCR. PathCLR’s (10-fold cross-validation) F1 score was 0.61 for CPCTR and 0.85 for JHU. This was statistically superior (paired t-test with P<.05) to the best-learned model that relied solely on clinicopathological features, including PSA level, primary and secondary Gleason Grade, etc. We attribute the improvement of PathCLR over models using only clinicopathological features to its utilization of both learned latent representations of tissue core images and clinicopathological features. This finding suggests that there is essential predictive information in tissue images at the time of surgery that goes beyond the knowledge obtained from reported clinicopathological features, helping predict the patient’s 5-year outcome.","PeriodicalId":37769,"journal":{"name":"Journal of Pathology Informatics","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2023-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135455776","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
An update on computational pathology tools for genitourinary pathology practice: A review paper from the Genitourinary Pathology Society (GUPS) 泌尿生殖系统病理实践中计算病理学工具的最新进展:泌尿生殖病理学会(GUPS)的一篇综述论文
Q2 Medicine Pub Date : 2023-01-01 DOI: 10.1016/j.jpi.2022.100177
Anil V. Parwani , Ankush Patel , Ming Zhou , John C. Cheville , Hamid Tizhoosh , Peter Humphrey , Victor E. Reuter , Lawrence D. True

Machine learning has been leveraged for image analysis applications throughout a multitude of subspecialties. This position paper provides a perspective on the evolutionary trajectory of practical deep learning tools for genitourinary pathology through evaluating the most recent iterations of such algorithmic devices. Deep learning tools for genitourinary pathology demonstrate potential to enhance prognostic and predictive capacity for tumor assessment including grading, staging, and subtype identification, yet limitations in data availability, regulation, and standardization have stymied their implementation.

机器学习已经被广泛应用于图像分析应用。本文通过评估这些算法设备的最新迭代,提供了实用深度学习工具用于泌尿生殖系统病理学的进化轨迹的视角。用于泌尿生殖系统病理学的深度学习工具显示出增强肿瘤评估(包括分级、分期和亚型识别)的预后和预测能力的潜力,但数据可用性、监管和标准化方面的限制阻碍了它们的实施。
{"title":"An update on computational pathology tools for genitourinary pathology practice: A review paper from the Genitourinary Pathology Society (GUPS)","authors":"Anil V. Parwani ,&nbsp;Ankush Patel ,&nbsp;Ming Zhou ,&nbsp;John C. Cheville ,&nbsp;Hamid Tizhoosh ,&nbsp;Peter Humphrey ,&nbsp;Victor E. Reuter ,&nbsp;Lawrence D. True","doi":"10.1016/j.jpi.2022.100177","DOIUrl":"10.1016/j.jpi.2022.100177","url":null,"abstract":"<div><p>Machine learning has been leveraged for image analysis applications throughout a multitude of subspecialties. This position paper provides a perspective on the evolutionary trajectory of practical deep learning tools for genitourinary pathology through evaluating the most recent iterations of such algorithmic devices. Deep learning tools for genitourinary pathology demonstrate potential to enhance prognostic and predictive capacity for tumor assessment including grading, staging, and subtype identification, yet limitations in data availability, regulation, and standardization have stymied their implementation.</p></div>","PeriodicalId":37769,"journal":{"name":"Journal of Pathology Informatics","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/72/90/main.PMC9841212.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9153396","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
期刊
Journal of Pathology Informatics
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
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
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1