MiThyCA: A Computational Pathology Pipeline for the Identification of Microscopic Foci of Papillary Thyroid Carcinoma-Like Nuclear Features with AI in Whole-Slide Histological Images.

IF 4.6 2区 医学 Q1 ENDOCRINOLOGY & METABOLISM
Leone Bacciu, Mario Urso, Vasco Coelho, Giorgio Cazzaniga, Angela Ida Pincelli, Mattia Garancini, Daniele M Papetti, Daniela Besozzi, Giulia Capitoli, Stefania Galimberti, Alessia Vargiolu, Nicola Fusco, Andrea Gianatti, Fabio Pagni, Vincenzo L'Imperio, Marco S Nobile
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引用次数: 0

Abstract

The histological identification of papillary thyroid carcinoma (PTC) is straightforward for experienced endocrine pathologists. The increase in radical thyroidectomies led to a raise in the rate of postoperative incidental subcentimeter PTC foci and the recent introduction of the Non-Invasive Follicular Thyroid Neoplasm with Papillary-like Nuclear Features (NIFTP) as a less aggressive mimicker of PTC, which significantly complicated the histology screening of thyroid histology specimens. Artificial Intelligence (AI) applied to Whole Slide Images (WSI) can speed up these processes, aiding pathologists to improve diagnostic accuracy and turnaround times. Here we present a computational pathology pipeline for the identification of Microscopic foci of papillary Thyroid Carcinoma-like nuclear features using Artificial intelligence (MiThyCA). This algorithm relies on a tandem architecture consisting of a Convolutional Neural Network (CNN) designed to identify neoplastic areas within thyroid specimens, and a Vision Transformer (TinyViT) focused on detecting PTC-like areas within the neoplastic regions identified by the first model. The study was conducted on a multi-institutional cohort of 73 WSIs from 67 patients with normal thyroid tissue (n = 22 patients, 33%), NIFTP (n = 19, 28%), PTC (n = 23, 34%), and lymph nodes (n = 3, 5%). Cases were divided into training (n = 40 patients, 41 WSIs), validation (n = 13 patients, 14 WSIs) and test (n = 14 patients, 18 WSIs) sets. Each model singly demonstrated excellent performance at the tile-level on the validation set (accuracy = 0.95 and AUC-ROC = 0.95 for CNN, accuracy = 0.86 and AUC-ROC = 0.84 for TinyViT), with their tandem combination in MiThyCA showing accuracy = 0.85 and F1 score = 0.8 on the validation set at the whole WSI-level. The average total execution time of MiThyCA on the test set WSIs was 51 ± 27 s on average on workstations not equipped with GPU, and up to 16 ± 6 s and 11 ± 4 s per WSI with Nvidia GPU and Apple's laptop chip, respectively. Worthy of note, WSIs dimension did not significantly impact the algorithm processing time. Given its speed and accessibility, MiThyCA is a promising AI-based computer-aided diagnostic tool for the detection of subcentimeter PTC foci in histology.

MiThyCA:利用人工智能在全片组织学图像中识别甲状腺乳头状癌样核特征的显微病灶的计算病理管道。
对于经验丰富的内分泌病理学家来说,甲状腺乳头状癌(PTC)的组织学鉴定是直截了当的。根治性甲状腺切除术的增加导致术后偶发亚厘米PTC灶的发生率增加,最近引入了具有乳头状核特征的无创滤泡性甲状腺肿瘤(NIFTP)作为PTC的低侵袭性模拟物,这大大增加了甲状腺组织学标本的组织学筛查。应用于全幻灯片图像(WSI)的人工智能(AI)可以加快这些过程,帮助病理学家提高诊断准确性和周转时间。在这里,我们提出了一种计算病理管道,用于使用人工智能(MiThyCA)识别乳头状甲状腺癌样核特征的显微病灶。该算法依赖于由卷积神经网络(CNN)组成的串联结构,该结构旨在识别甲状腺标本中的肿瘤区域,而视觉变压器(TinyViT)专注于检测由第一个模型识别的肿瘤区域内的ptc样区域。该研究对来自67例甲状腺组织正常(n = 22例,33%)、NIFTP (n = 19, 28%)、PTC (n = 23, 34%)和淋巴结(n = 3.5%)的73例wsi患者进行了多机构队列研究。病例分为训练组(n = 40例,41例wsi)、验证组(n = 13例,14例wsi)和试验组(n = 14例,18例wsi)。每个模型单独在验证集上都表现出优异的瓦片级性能(CNN的准确率为0.95,AUC-ROC = 0.95, TinyViT的准确率为0.86,AUC-ROC = 0.84),它们在MiThyCA中的串联组合在整个wsi水平上的验证集上的准确率为0.85,F1得分为0.8。MiThyCA在测试集WSI上的平均总执行时间在未配备GPU的工作站上平均为51±27 s,在使用Nvidia GPU和Apple笔记本电脑芯片的WSI上分别高达16±6 s和11±4 s。值得注意的是,wsi维数对算法处理时间没有显著影响。鉴于其速度和可及性,MiThyCA是一种有前途的基于人工智能的计算机辅助诊断工具,用于检测组织学中的亚厘米PTC病灶。
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来源期刊
Endocrine Pathology
Endocrine Pathology 医学-病理学
CiteScore
12.30
自引率
20.50%
发文量
41
审稿时长
>12 weeks
期刊介绍: Endocrine Pathology publishes original articles on clinical and basic aspects of endocrine disorders. Work with animals or in vitro techniques is acceptable if it is relevant to human normal or abnormal endocrinology. Manuscripts will be considered for publication in the form of original articles, case reports, clinical case presentations, reviews, and descriptions of techniques. Submission of a paper implies that it reports unpublished work, except in abstract form, and is not being submitted simultaneously to another publication. Accepted manuscripts become the sole property of Endocrine Pathology and may not be published elsewhere without written consent from the publisher. All articles are subject to review by experienced referees. The Editors and Editorial Board judge manuscripts suitable for publication, and decisions by the Editors are final.
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