Hybrid deep multi-task learning radiomics approach for predicting EGFR mutation status of non-small cell lung cancer in CT images

队列 接收机工作特性 无线电技术 人工智能 肺癌 特征(语言学) 深度学习 医学 肿瘤科 计算机科学 放射科 内科学 语言学 哲学
作者
Jing Gong,Fangqiu Fu,Xiaowen Ma,Ting Wang,Xiangyi Ma,Chao You,Yang Zhang,Weijun Peng,Haiquan Chen,Yajia Gu
出处
期刊:Physics in Medicine and Biology [IOP Publishing]
卷期号:68 (24): 245021-245021 被引量:11
标识
DOI:10.1088/1361-6560/ad0d43
摘要

Abstract Objective. Epidermal growth factor receptor (EGFR) mutation genotyping plays a pivotal role in targeted therapy for non-small cell lung cancer (NSCLC). We aimed to develop a computed tomography (CT) image-based hybrid deep radiomics model to predict EGFR mutation status in NSCLC and investigate the correlations between deep image and quantitative radiomics features. Approach. First, we retrospectively enrolled 818 patients from our centre and 131 patients from The Cancer Imaging Archive database to establish a training cohort ( N = 654), an independent internal validation cohort ( N = 164) and an external validation cohort ( N = 131). Second, to predict EGFR mutation status, we developed three CT image-based models, namely, a multi-task deep neural network (DNN), a radiomics model and a feature fusion model. Third, we proposed a hybrid loss function to train the DNN model. Finally, to evaluate the model performance, we computed the areas under the receiver operating characteristic curves (AUCs) and decision curve analysis curves of the models. Main results. For the two validation cohorts, the feature fusion model achieved AUC values of 0.86 ± 0.03 and 0.80 ± 0.05, which were significantly higher than those of the single-task DNN and radiomics models (all P < 0.05). There was no significant difference between the feature fusion and the multi-task DNN models ( P > 0.8). The binary prediction scores showed excellent prognostic value in predicting disease-free survival ( P = 0.02) and overall survival ( P < 0.005) for validation cohort 2. Significance. The results demonstrate that (1) the feature fusion and multi-task DNN models achieve significantly higher performance than that of the conventional radiomics and single-task DNN models, (2) the feature fusion model can decode the imaging phenotypes representing NSCLC heterogeneity related to both EGFR mutation and patient NSCLC prognosis, and (3) high correlations exist between some deep image and radiomics features.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
ET发布了新的文献求助10
刚刚
WXYZ发布了新的文献求助10
刚刚
ZetianYang发布了新的文献求助10
刚刚
田田田发布了新的文献求助10
刚刚
CLW发布了新的文献求助10
2秒前
Moon完成签到,获得积分10
4秒前
WANG发布了新的文献求助10
6秒前
Alex完成签到 ,获得积分10
7秒前
北城发布了新的文献求助10
8秒前
Lemon完成签到,获得积分10
9秒前
骑士完成签到,获得积分10
9秒前
9秒前
12秒前
骑士发布了新的文献求助100
12秒前
Moon发布了新的文献求助10
13秒前
15秒前
慢吞吞完成签到,获得积分10
15秒前
黄上权发布了新的文献求助20
18秒前
专注的语堂完成签到,获得积分10
19秒前
黑白完成签到,获得积分10
20秒前
21秒前
gyh完成签到,获得积分20
23秒前
寻梦发布了新的文献求助10
24秒前
25秒前
爱撒娇的妙竹完成签到,获得积分10
25秒前
追寻连虎发布了新的文献求助10
26秒前
27秒前
甜甜绮烟完成签到 ,获得积分10
27秒前
淡然的咖啡豆完成签到,获得积分10
28秒前
火星上牛排完成签到,获得积分10
29秒前
田田田发布了新的文献求助10
29秒前
29秒前
芳菲落尽梨花白完成签到 ,获得积分10
31秒前
时零完成签到 ,获得积分10
32秒前
曾经的芫发布了新的文献求助10
35秒前
Eason完成签到,获得积分10
36秒前
37秒前
暴躁的水蜜桃完成签到 ,获得积分10
37秒前
cloud完成签到,获得积分10
38秒前
暗眸发布了新的文献求助10
38秒前
高分求助中
Principles of Economics, 11th Edition 10000
University Physics with Modern Physics, 16th edition 10000
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Gründe der Seele:Die Wiener Psychatrie im 20.Jahrhundert 1000
Development of a Bridge Weigh-In-Motion System: A technology to convert the bridge response to the passage of traffic into data on vehicle configurations, speeds, times of travel and weights 1000
Organic Reactions, Volume 116 1000
Current concepts in cutaneous toxicity : proceedings of the Fourth Conference on Cutaneous Toxicity, Washington, D.C., May 9-11, 1979 1000
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7272349
求助须知:如何正确求助?哪些是违规求助? 8893211
关于积分的说明 18800282
捐赠科研通 6946770
什么是DOI,文献DOI怎么找? 3204705
关于科研通互助平台的介绍 2376889
邀请新用户注册赠送积分活动 2180178