Development and External Validation of an Improved Version of the Diagnostic Model for Opportunistic Screening of Malignant Esophageal Lesions

We aimed to develop an improved version of the diagnostic model predicting the risk of malignant esophageal lesions in opportunistic screening and validate it in external populations. The development set involved 10,595 outpatients receiving endoscopy from a hospital in Hua County, a high-risk regio...

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Main Authors: Zhen Liu, Hongchen Zheng, Mengfei Liu, Yujie He, Yun Chen, Ping Ji, Zhengyu Fang, Ping Xiao, Fenglei Li, Chuanhai Guo, Weihua Yin, Yaqi Pan, Zhonghu He, Yang Ke
Format: Article
Language:English
Published: MDPI AG 2022-11-01
Series:Cancers
Subjects:
Online Access:https://www.mdpi.com/2072-6694/14/23/5945
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author Zhen Liu
Hongchen Zheng
Mengfei Liu
Yujie He
Yun Chen
Ping Ji
Zhengyu Fang
Ping Xiao
Fenglei Li
Chuanhai Guo
Weihua Yin
Yaqi Pan
Zhonghu He
Yang Ke
author_facet Zhen Liu
Hongchen Zheng
Mengfei Liu
Yujie He
Yun Chen
Ping Ji
Zhengyu Fang
Ping Xiao
Fenglei Li
Chuanhai Guo
Weihua Yin
Yaqi Pan
Zhonghu He
Yang Ke
author_sort Zhen Liu
collection DOAJ
description We aimed to develop an improved version of the diagnostic model predicting the risk of malignant esophageal lesions in opportunistic screening and validate it in external populations. The development set involved 10,595 outpatients receiving endoscopy from a hospital in Hua County, a high-risk region for esophageal squamous cell carcinoma in northern China. Validation set A enrolled 9453 outpatients receiving endoscopy in a non-high-risk region in southern China. Validation set B involved 17,511 residents in Hua County. The improved diagnostic model consisted of seven predictors including age, gender, family history of esophageal squamous cell carcinoma, smoking, body mass index, dysphagia, and retrosternal pain, with an area under the receiver operating characteristic curve (AUC) of 0.860 (95% confidence interval: 0.835–0.886) in the development set. Ideal discrimination ability was achieved in external validations (AUC <sub>validation set A</sub>: 0.892, 95% confidence interval: 0.858–0.926; AUC <sub>validation set B</sub>: 0.799, 95% confidence interval: 0.705–0.894). This improved model also markedly increased the detection rate of malignant esophageal lesions compared with universal screening, demonstrating great potential for use in opportunistic screening of malignant esophageal lesions in heterogeneous populations.
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spelling doaj.art-fefc4e1d0f01485b8b55ec13145858b22023-11-24T10:41:15ZengMDPI AGCancers2072-66942022-11-011423594510.3390/cancers14235945Development and External Validation of an Improved Version of the Diagnostic Model for Opportunistic Screening of Malignant Esophageal LesionsZhen Liu0Hongchen Zheng1Mengfei Liu2Yujie He3Yun Chen4Ping Ji5Zhengyu Fang6Ping Xiao7Fenglei Li8Chuanhai Guo9Weihua Yin10Yaqi Pan11Zhonghu He12Yang Ke13Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Laboratory of Genetics, Peking University Cancer Hospital & Institute, Beijing 100142, ChinaKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Laboratory of Genetics, Peking University Cancer Hospital & Institute, Beijing 100142, ChinaKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Laboratory of Genetics, Peking University Cancer Hospital & Institute, Beijing 100142, ChinaEndoscopy Center, Hua County People’s Hospital, Hua County 456483, ChinaDepartment of Ultrasound, Peking University Shenzhen Hospital, Shenzhen 518034, ChinaClinical Research Institute, Shenzhen Peking University-Hong Kong University of Science and Technology Medical Center, Shenzhen 518034, ChinaClinical Research Institute, Shenzhen Peking University-Hong Kong University of Science and Technology Medical Center, Shenzhen 518034, ChinaClinical Research Institute, Shenzhen Peking University-Hong Kong University of Science and Technology Medical Center, Shenzhen 518034, ChinaHua County People’s Hospital, Hua County 456483, ChinaKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Laboratory of Genetics, Peking University Cancer Hospital & Institute, Beijing 100142, ChinaDepartment of Pathology, Peking University Shenzhen Hospital, Shenzhen 518034, ChinaKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Laboratory of Genetics, Peking University Cancer Hospital & Institute, Beijing 100142, ChinaKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Laboratory of Genetics, Peking University Cancer Hospital & Institute, Beijing 100142, ChinaKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Laboratory of Genetics, Peking University Cancer Hospital & Institute, Beijing 100142, ChinaWe aimed to develop an improved version of the diagnostic model predicting the risk of malignant esophageal lesions in opportunistic screening and validate it in external populations. The development set involved 10,595 outpatients receiving endoscopy from a hospital in Hua County, a high-risk region for esophageal squamous cell carcinoma in northern China. Validation set A enrolled 9453 outpatients receiving endoscopy in a non-high-risk region in southern China. Validation set B involved 17,511 residents in Hua County. The improved diagnostic model consisted of seven predictors including age, gender, family history of esophageal squamous cell carcinoma, smoking, body mass index, dysphagia, and retrosternal pain, with an area under the receiver operating characteristic curve (AUC) of 0.860 (95% confidence interval: 0.835–0.886) in the development set. Ideal discrimination ability was achieved in external validations (AUC <sub>validation set A</sub>: 0.892, 95% confidence interval: 0.858–0.926; AUC <sub>validation set B</sub>: 0.799, 95% confidence interval: 0.705–0.894). This improved model also markedly increased the detection rate of malignant esophageal lesions compared with universal screening, demonstrating great potential for use in opportunistic screening of malignant esophageal lesions in heterogeneous populations.https://www.mdpi.com/2072-6694/14/23/5945esophageal squamous cell carcinomaopportunistic screeningdiagnostic modelmodel updatingexternal validation
spellingShingle Zhen Liu
Hongchen Zheng
Mengfei Liu
Yujie He
Yun Chen
Ping Ji
Zhengyu Fang
Ping Xiao
Fenglei Li
Chuanhai Guo
Weihua Yin
Yaqi Pan
Zhonghu He
Yang Ke
Development and External Validation of an Improved Version of the Diagnostic Model for Opportunistic Screening of Malignant Esophageal Lesions
Cancers
esophageal squamous cell carcinoma
opportunistic screening
diagnostic model
model updating
external validation
title Development and External Validation of an Improved Version of the Diagnostic Model for Opportunistic Screening of Malignant Esophageal Lesions
title_full Development and External Validation of an Improved Version of the Diagnostic Model for Opportunistic Screening of Malignant Esophageal Lesions
title_fullStr Development and External Validation of an Improved Version of the Diagnostic Model for Opportunistic Screening of Malignant Esophageal Lesions
title_full_unstemmed Development and External Validation of an Improved Version of the Diagnostic Model for Opportunistic Screening of Malignant Esophageal Lesions
title_short Development and External Validation of an Improved Version of the Diagnostic Model for Opportunistic Screening of Malignant Esophageal Lesions
title_sort development and external validation of an improved version of the diagnostic model for opportunistic screening of malignant esophageal lesions
topic esophageal squamous cell carcinoma
opportunistic screening
diagnostic model
model updating
external validation
url https://www.mdpi.com/2072-6694/14/23/5945
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