Large-scale esophageal cancer screening through noncontrast computed tomography and artificial intelligence

IF 52.5 1区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Jian Zhou, Guangyu Guo, Jiawen Yao, Qinji Yu, Chunpeng Zheng, Xiaochen Feng, Xianghua Ye, Yongjin Zhou, Pei Yang, Lukas Lambert, Shaojun Zheng, Qiong Li, Yingda Xia, Wenchao Guo, Yi Chen, Mengdi Zhang, Yu Jiang, Dandan Zheng, Jia Ge, Haomiao Qing, Wusong Liu, Peng Zhou, Mei Lan, Lei Wu, Yong Li, Haifeng Wang, Yong Zhou, Junqiang Chen, Liyan Xu, Chenying Lu, Lin Chen, Junwei Han, Chengwei Shao, Wenqiang Wei, Kai Zhang, Jianfeng Zhang, Dingwen Zhang, Jiansong Ji, Na Li, Chuanmiao Xie, Kai Cao, Yuqian Zhao, Ling Zhang, Qifeng Wang
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引用次数: 0

Abstract

The absence of accurate, noninvasive, scalable screening tools keeps early esophageal cancer (EC) detection a global health challenge. Although noncontrast computed tomography (NC CT) is widely accessible, the esophagus is a hollow tubular structure prone to collapse and motion artifacts, making small early malignant lesions difficult to distinguish from normal tissue. Here we developed the Esophageal AI-Guided malignant Lesion Evaluation (EAGLE) model to detect precancerous lesions and cancer from chest NC CT, a task historically considered impossible. EAGLE was trained on 6,813 patients from two centers and validated across 12 centers in three countries involving 80,612 patients in opportunistic and population-based screening settings. For opportunistic screening on existing CT scans, multicenter external test cohorts (eight centers, n = 11,466) achieved 98.5% specificity, with 90.0% sensitivity for cancer and 52.5% for precancerous lesions; low-dose CT (LDCT) validation (two centers, n = 1,607) showed comparable performance, supporting EC screening through lung-cancer screening programs. Calibration in a real-world cohort (three centers, n = 35,402) reduced false positives by 72.7% while preserving sensitivity; prospective hospital validation (n = 17,446) achieved a 42.2% PPV, and real-world low-dose screening (n = 10,959) reached 99.94% specificity. EAGLE also detected precancerous lesions—in paired CT–endoscopy cohorts (two centers, n = 702), sensitivities were 65.0% for precancerous lesions and 78.4% for stage I EC at a higher-sensitivity operating point. Exploratory analyses of a prospectively enrolled cohort suggest that referring high-risk individuals for endoscopy could improve screening efficiency. In conclusion, EAGLE has the potential to serve as a scalable tool for early EC screening. Chictr.org.cn identifier: ChiCTR2300074806 . In a large-scale study, a new tool called Esophageal AI-Guided malignant Lesion Evaluation uses artificial intelligence to enhance esophageal cancer detection through noncontrast computed tomography, achieving high sensitivity and specificity across diverse settings.
通过非对比计算机断层扫描和人工智能进行大规模食管癌筛查
缺乏准确、无创、可扩展的筛查工具使早期食管癌(EC)检测成为全球健康挑战。虽然非对比计算机断层扫描(NC CT)广泛使用,但食管是一个空心管状结构,容易塌陷和运动伪影,使得早期的小恶性病变难以与正常组织区分。在这里,我们开发了食管ai引导的恶性病变评估(EAGLE)模型,用于从胸部NC CT检测癌前病变和癌症,这在历史上被认为是不可能的任务。EAGLE对来自两个中心的6813名患者进行了培训,并在三个国家的12个中心进行了验证,涉及80612名患者,进行了机会性和基于人群的筛查。对于现有CT扫描的机会性筛查,多中心外部测试队列(8个中心,n = 11,466)的特异性为98.5%,对癌症的敏感性为90.0%,对癌前病变的敏感性为52.5%;低剂量CT (LDCT)验证(两个中心,n = 1,607)显示出相当的性能,通过肺癌筛查项目支持EC筛查。在真实世界队列(三个中心,n = 35402)中进行校准,在保持灵敏度的同时,误报率降低了72.7%;前瞻性医院验证(n = 17,446)达到42.2%的PPV,实际低剂量筛查(n = 10,959)达到99.94%的特异性。EAGLE也检测到癌前病变——在配对ct -内镜队列中(两个中心,n = 702),在更高灵敏度的手术点,癌前病变的敏感性为65.0%,期EC的敏感性为78.4%。一项前瞻性入组队列的探索性分析表明,推荐高危人群进行内窥镜检查可以提高筛查效率。总之,EAGLE有潜力作为早期EC筛查的可扩展工具。标识符:ChiCTR2300074806。在一项大规模研究中,一种名为“食管人工智能引导恶性病变评估”的新工具使用人工智能来增强通过非对比计算机断层扫描检测食管癌的能力,在不同环境下实现高灵敏度和高特异性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Nature Medicine
Nature Medicine 医学-生化与分子生物学
CiteScore
100.90
自引率
0.70%
发文量
525
审稿时长
1 months
期刊介绍: Nature Medicine is a monthly journal publishing original peer-reviewed research in all areas of medicine. The publication focuses on originality, timeliness, interdisciplinary interest, and the impact on improving human health. In addition to research articles, Nature Medicine also publishes commissioned content such as News, Reviews, and Perspectives. This content aims to provide context for the latest advances in translational and clinical research, reaching a wide audience of M.D. and Ph.D. readers. All editorial decisions for the journal are made by a team of full-time professional editors. Nature Medicine consider all types of clinical research, including: -Case-reports and small case series -Clinical trials, whether phase 1, 2, 3 or 4 -Observational studies -Meta-analyses -Biomarker studies -Public and global health studies Nature Medicine is also committed to facilitating communication between translational and clinical researchers. As such, we consider “hybrid” studies with preclinical and translational findings reported alongside data from clinical studies.
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