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A new model using deep learning to predict recurrence after surgical resection of lung adenocarcinoma

腺癌 切除术 外科切除术 计算机科学 人工智能 医学 外科 普通外科 内科学 癌症
作者
Pil-Jong Kim,Hyeon-Shik Hwang,Gyuheon Choi,Hyun-Jung Sung,Bokyung Ahn,Jinsoo Uh,Shinkyo Yoon,Deokhoon Kim,Sung Chun,Se Jin Jang,Heounjeong Go
出处
期刊:Scientific Reports [Springer Nature]
卷期号:14 (1)
标识
DOI:10.1038/s41598-024-56867-9
摘要

Abstract This study aimed to develop a deep learning (DL) model for predicting the recurrence risk of lung adenocarcinoma (LUAD) based on its histopathological features. Clinicopathological data and whole slide images from 164 LUAD cases were collected and used to train DL models with an ImageNet pre-trained efficientnet-b2 architecture, densenet201, and resnet152. The models were trained to classify each image patch into high-risk or low-risk groups, and the case-level result was determined by multiple instance learning with final FC layer’s features from a model from all patches. Analysis of the clinicopathological and genetic characteristics of the model-based risk group was performed. For predicting recurrence, the model had an area under the curve score of 0.763 with 0.750, 0.633 and 0.680 of sensitivity, specificity, and accuracy in the test set, respectively. High-risk cases for recurrence predicted by the model (HR group) were significantly associated with shorter recurrence-free survival and a higher stage (both, p < 0.001). The HR group was associated with specific histopathological features such as poorly differentiated components, complex glandular pattern components, tumor spread through air spaces, and a higher grade. In the HR group, pleural invasion, necrosis, and lymphatic invasion were more frequent, and the size of the invasion was larger (all, p < 0.001). Several genetic mutations, including TP53 ( p = 0.007) mutations, were more frequently found in the HR group. The results of stages I-II were similar to those of the general cohort. DL-based model can predict the recurrence risk of LUAD and identify the presence of the TP53 gene mutation by analyzing histopathologic features.

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