Department of Pathology, Kurume University School of Medicine, Kurume, 830-0011, Japan.
Department of Diagnostic Pathology, Kurume University Hospital, Kurume, 830-0011, Japan.
Sci Rep. 2021 Apr 19;11(1):8454. doi: 10.1038/s41598-021-87748-0.
Histopathological diagnosis of pancreatic ductal adenocarcinoma (PDAC) on endoscopic ultrasonography-guided fine-needle biopsy (EUS-FNB) specimens has become the mainstay of preoperative pathological diagnosis. However, on EUS-FNB specimens, accurate histopathological evaluation is difficult due to low specimen volume with isolated cancer cells and high contamination of blood, inflammatory and digestive tract cells. In this study, we performed annotations for training sets by expert pancreatic pathologists and trained a deep learning model to assess PDAC on EUS-FNB of the pancreas in histopathological whole-slide images. We obtained a high receiver operator curve area under the curve of 0.984, accuracy of 0.9417, sensitivity of 0.9302 and specificity of 0.9706. Our model was able to accurately detect difficult cases of isolated and low volume cancer cells. If adopted as a supportive system in routine diagnosis of pancreatic EUS-FNB specimens, our model has the potential to aid pathologists diagnose difficult cases.
在内镜超声引导下细针穿刺活检 (EUS-FNB) 标本中对胰腺导管腺癌 (PDAC) 进行组织病理学诊断已成为术前病理诊断的主要方法。然而,在 EUS-FNB 标本中,由于标本体积小,仅含有孤立的癌细胞,且血液、炎症和消化道细胞污染严重,因此准确的组织病理学评估较为困难。在这项研究中,我们由胰腺病理专家对训练集进行标注,并训练了一个深度学习模型,以评估胰腺 EUS-FNB 组织病理全切片图像中的 PDAC。我们得到了高接收者操作曲线下的曲线面积为 0.984、准确率为 0.9417、敏感度为 0.9302 和特异性为 0.9706。我们的模型能够准确地检测到孤立和低体积癌细胞的困难病例。如果将其作为胰腺 EUS-FNB 标本常规诊断的辅助系统采用,我们的模型有可能帮助病理学家诊断困难病例。