Predicting the pathological status of mammographic microcalcifications through a radiomics approach

IF 4.4 Q1 COMPUTER SCIENCE, INTERDISCIPLINARY APPLICATIONS
Min Li , Liyu Zhu , Guangquan Zhou , Jianan He , Yanni Jiang , Yang Chen
{"title":"Predicting the pathological status of mammographic microcalcifications through a radiomics approach","authors":"Min Li ,&nbsp;Liyu Zhu ,&nbsp;Guangquan Zhou ,&nbsp;Jianan He ,&nbsp;Yanni Jiang ,&nbsp;Yang Chen","doi":"10.1016/j.imed.2021.05.003","DOIUrl":null,"url":null,"abstract":"<div><p><strong>Objective</strong> The study aimed to develop a machine learning (ML)-coupled interpretable radiomics signature to predict the pathological status of non-palpable suspicious breast microcalcifications (MCs).</p><p><strong>Methods</strong> We enrolled 463 digital mammographical view images from 260 consecutive patients detected with non-palpable MCs and BI-RADS scored at 4 (training cohort, <em>n</em> = 428; independent testing cohort, <em>n</em> = 35) in the First Affiliated Hospital of Nanjing Medical University between September 2010 and January 2019. Subsequently, 837 textures and 9 shape features were subsequently extracted from each view and finally selected by an XGBoost-embedded recursive feature elimination technique (RFE), followed by four machine learning-based classifiers to build the radiomics signature.</p><p><strong>Results</strong> Ten radiomic features constituted a malignancy-related signature for breast MCs as logistic regression (LR) and support vector machine (SVM) yielded better positive predictive value (PPV)/sensitivity (SE), 0.904 (95% CI, 0.865–0.949)/0.946 (95% CI, 0.929–0.977) and 0.891 (95% CI, 0.822–0.939)/0.939 (95% CI, 0.907–0.973) respectively, outperforming their negative predictive value (NPV)/specificity (SP) from 10-fold cross-validation (10FCV) of the training cohort. The optimal prognostic model was obtained by SVM with an area under the curve (AUC) of 0.906 (95% CI, 0.834–0.969) and accuracy (ACC) 0.787 (95% CI, 0.680–0.855) from 10FCV against AUC 0.810 (95% CI, 0.760–0.960) and ACC 0.800 from the testing cohort.</p><p><strong>Conclusion</strong> The proposed radiomics signature dependens on a set of ML-based advanced computational algorithms and is expected to identify pathologically cancerous cases from mammographically undecipherable MCs and thus offer prospective clinical diagnostic guidance.</p></div>","PeriodicalId":73400,"journal":{"name":"Intelligent medicine","volume":"1 3","pages":"Pages 95-103"},"PeriodicalIF":4.4000,"publicationDate":"2021-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.imed.2021.05.003","citationCount":"3","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Intelligent medicine","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2667102621000127","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"COMPUTER SCIENCE, INTERDISCIPLINARY APPLICATIONS","Score":null,"Total":0}
引用次数: 3

Abstract

Objective The study aimed to develop a machine learning (ML)-coupled interpretable radiomics signature to predict the pathological status of non-palpable suspicious breast microcalcifications (MCs).

Methods We enrolled 463 digital mammographical view images from 260 consecutive patients detected with non-palpable MCs and BI-RADS scored at 4 (training cohort, n = 428; independent testing cohort, n = 35) in the First Affiliated Hospital of Nanjing Medical University between September 2010 and January 2019. Subsequently, 837 textures and 9 shape features were subsequently extracted from each view and finally selected by an XGBoost-embedded recursive feature elimination technique (RFE), followed by four machine learning-based classifiers to build the radiomics signature.

Results Ten radiomic features constituted a malignancy-related signature for breast MCs as logistic regression (LR) and support vector machine (SVM) yielded better positive predictive value (PPV)/sensitivity (SE), 0.904 (95% CI, 0.865–0.949)/0.946 (95% CI, 0.929–0.977) and 0.891 (95% CI, 0.822–0.939)/0.939 (95% CI, 0.907–0.973) respectively, outperforming their negative predictive value (NPV)/specificity (SP) from 10-fold cross-validation (10FCV) of the training cohort. The optimal prognostic model was obtained by SVM with an area under the curve (AUC) of 0.906 (95% CI, 0.834–0.969) and accuracy (ACC) 0.787 (95% CI, 0.680–0.855) from 10FCV against AUC 0.810 (95% CI, 0.760–0.960) and ACC 0.800 from the testing cohort.

Conclusion The proposed radiomics signature dependens on a set of ML-based advanced computational algorithms and is expected to identify pathologically cancerous cases from mammographically undecipherable MCs and thus offer prospective clinical diagnostic guidance.

通过放射组学方法预测乳房x线微钙化的病理状态
目的建立一种机器学习(ML)耦合的可解释放射组学特征来预测不可触及的可疑乳房微钙化(MCs)的病理状态。方法:我们收集了260例连续检测到不可触及MCs的患者的463张数字乳房x线摄影图像,BI-RADS评分为4(训练队列,n = 428;独立检测队列,n = 35),于2010年9月至2019年1月在南京医科大学第一附属医院进行。随后,从每个视图中提取837个纹理和9个形状特征,最后通过嵌入xgboost的递归特征消除技术(RFE)进行选择,然后使用4个基于机器学习的分类器构建放射组学签名。结果10个放射学特征构成乳腺MCs的恶性相关特征,logistic回归(LR)和支持向量机(SVM)的阳性预测值(PPV)/敏感性(SE)更高,分别为0.904 (95% CI, 0.865-0.949)/0.946 (95% CI, 0.929-0.977)和0.891 (95% CI, 0.822-0.939)/0.939 (95% CI, 0.907-0.973),优于训练队列10倍交叉验证(10FCV)的阴性预测值(NPV)/特异性(SP)。通过支持向量机获得最佳预后模型,曲线下面积(AUC)为0.906 (95% CI, 0.834-0.969),准确度(ACC)为0.787 (95% CI, 0.680-0.855),而测试队列的AUC为0.810 (95% CI, 0.760-0.960), ACC为0.800。结论提出的放射组学特征依赖于一套基于ml的先进计算算法,有望从乳房x线摄影无法识别的MCs中识别病理癌病例,从而提供前瞻性临床诊断指导。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Intelligent medicine
Intelligent medicine Surgery, Radiology and Imaging, Artificial Intelligence, Biomedical Engineering
CiteScore
5.20
自引率
0.00%
发文量
19
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信