4.6 Article

A deep learning model using hyperspectral image for EUS-FNA cytology diagnosis in pancreatic ductal adenocarcinoma

Journal

CANCER MEDICINE
Volume -, Issue -, Pages -

Publisher

WILEY
DOI: 10.1002/cam4.6335

Keywords

artificial intelligence; deep learning; endoscopic ultrasound-guided fine-needle aspiration; neural network models; pancreatic ductal carcinoma

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In this study, a hyperspectral imaging-based convolutional neural network algorithm was developed to assist in the diagnosis of pancreatic cancer using endoscopic ultrasonography-guided fine-needle aspiration cytology specimens. The model showed high accuracy, sensitivity, and specificity in distinguishing between malignant and benign pancreatic cells. These findings suggest that the model has important clinical implications in the field of cytological diagnosis.
Background and Aims: Endoscopic ultrasonography-guided fine-needle aspiration/biopsy (EUS-FNA/B) is considered to be a first-line procedure for the pathological diagnosis of pancreatic cancer owing to its high accuracy and low complication rate. The number of new cases of pancreatic ductal adenocarcinoma (PDAC) is increasing, and its accurate pathological diagnosis poses a challenge for cytopathologists. Our aim was to develop a hyperspectral imaging (HSI)-based convolution neural network (CNN) algorithm to aid in the diagnosis of pancreatic EUS-FNA cytology specimens.Methods: HSI images were captured of pancreatic EUS-FNA cytological specimens from benign pancreatic tissues (n = 33) and PDAC (n = 39) prepared using a liquid-based cytology method. A CNN was established to test the diagnostic performance, and Attribution Guided Factorization Visualization (AGF-Visualization) was used to visualize the regions of important classification features identified by the model.Results: A total of 1913 HSI images were obtained. Our ResNet18-SimSiam model achieved an accuracy of 0.9204, sensitivity of 0.9310 and specificity of 0.9123 (area under the curve of 0.9625) when trained on HSI images for the differentiation of PDAC cytological specimens from benign pancreatic cells. AGF-Visualization confirmed that the diagnoses were based on the features of tumor cell nuclei.Conclusions: An HSI-based model was developed to diagnose cytological PDAC specimens obtained using EUS-guided sampling. Under the supervision of experienced cytopathologists, we performed multi-staged consecutive in-depth learning of the model. Its superior diagnostic performance could be of value for cytologists when diagnosing PDAC.

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