医学
人工智能
基本事实
淋巴结
结直肠癌
接收机工作特性
分割
深度学习
H&E染色
计算机科学
病理
模式识别(心理学)
放射科
癌症
内科学
染色
作者
Amjad Khan,Nelleke P.M. Brouwer,Annika Blank,F. Müller,Davide Soldini,Aurelia Noske,Elisabeth Gaus,Simone Brandt,Irıs D. Nagtegaal,Heather Dawson,Jean‐Philippe Thiran,Aurel Perren,Alessandro Lugli,Inti Zlobec
出处
期刊:Modern Pathology
[Elsevier BV]
日期:2023-02-02
卷期号:36 (5): 100118-100118
被引量:34
标识
DOI:10.1016/j.modpat.2023.100118
摘要
Screening of lymph node metastases in colorectal cancer (CRC) can be a cumbersome task, but it is amenable to artificial intelligence (AI)-assisted diagnostic solution. Here, we propose a deep learning-based workflow for the evaluation of CRC lymph node metastases from digitized hematoxylin and eosin (HE)-stained sections. A segmentation model was trained on 100 whole slide images (WSIs). It achieved a Matthews correlation coefficient (MCC) of 0.86 (± 0.154) and an acceptable Hausdorff Distance (HD) range of 135.59 μm (± 72.14 μm), indicating a high congruence with ground truth. For metastasis detection, two models (Xception and Vision Transform) were independently trained first on a patch-based breast cancer lymph node dataset and were then fine-tuned using the CRC dataset. After fine-tuning, the ensemble model showed significant improvements in the F1 score (0.797 – 0.949, p < 0.00001) and the area under the receiver operating characteristic curve (0.959 – 0.978, p < 0.00001). Four independent cohorts (three internal, one external) of CRC lymph nodes were used for validation in cascading segmentation and metastasis-detection models. Our approach showed excellent performance, with high sensitivity (0.995, 1.0) and specificity (0.967, 1.0) in two validation cohorts of adenocarcinoma cases (n = 3836 slides) when comparing slide-level labels with ground truth (pathologists reports). Similarly, an acceptable performance was achieved in a validation cohort (n = 172 slides) with mucinous and signet-ring cell histology (sensitivity: 0.872 and specificity: 0.936). The patch-based classification confidence was aggregated to overlay the potential metastatic regions within each lymph node slide for visualization. We also applied our method to a consecutive case series of lymph nodes obtained over the last 6 months at our institute (n = 217 slides). The overlays of prediction within lymph node regions matched 100% when compared with a microscope evaluation by an expert pathologist. Our results provide the basis for a computer-assisted diagnostic tool for easy and efficient lymph node screening in CRC patients.
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