TY - JOUR
T1 - A Classifier for Improving Early Lung Cancer Diagnosis Incorporating Artificial Intelligence and Liquid Biopsy
AU - Ye, Maosong
AU - Tong, Lin
AU - Zheng, Xiaoxuan
AU - Wang, Hui
AU - Zhou, Haining
AU - Zhu, Xiaoli
AU - Zhou, Chengzhi
AU - Zhao, Peige
AU - Wang, Yan
AU - Wang, Qi
AU - Bai, Li
AU - Cai, Zhigang
AU - Kong, Feng Ming
AU - Wang, Yuehong
AU - Li, Yafei
AU - Feng, Mingxiang
AU - Ye, Xin
AU - Yang, Dawei
AU - Liu, Zilong
AU - Zhang, Quncheng
AU - Wang, Ziqi
AU - Han, Shuhua
AU - Sun, Lihong
AU - Zhao, Ningning
AU - Yu, Zubin
AU - Zhang, Juncheng
AU - Zhang, Xiaoju
AU - Katz, Ruth L.
AU - Sun, Jiayuan
AU - Bai, Chunxue
N1 - Publisher Copyright:
Copyright © 2022 Ye, Tong, Zheng, Wang, Zhou, Zhu, Zhou, Zhao, Wang, Wang, Bai, Cai, Kong, Wang, Li, Feng, Ye, Yang, Liu, Zhang, Wang, Han, Sun, Zhao, Yu, Zhang, Zhang, Katz, Sun and Bai.
PY - 2022/3/2
Y1 - 2022/3/2
N2 - Lung cancer is the leading cause of cancer-related deaths worldwide and in China. Screening for lung cancer by low dose computed tomography (LDCT) can reduce mortality but has resulted in a dramatic rise in the incidence of indeterminate pulmonary nodules, which presents a major diagnostic challenge for clinicians regarding their underlying pathology and can lead to overdiagnosis. To address the significant gap in evaluating pulmonary nodules, we conducted a prospective study to develop a prediction model for individuals at intermediate to high risk of developing lung cancer. Univariate and multivariate logistic analyses were applied to the training cohort (n = 560) to develop an early lung cancer prediction model. The results indicated that a model integrating clinical characteristics (age and smoking history), radiological characteristics of pulmonary nodules (nodule diameter, nodule count, upper lobe location, malignant sign at the nodule edge, subsolid status), artificial intelligence analysis of LDCT data, and liquid biopsy achieved the best diagnostic performance in the training cohort (sensitivity 89.53%, specificity 81.31%, area under the curve [AUC] = 0.880). In the independent validation cohort (n = 168), this model had an AUC of 0.895, which was greater than that of the Mayo Clinic Model (AUC = 0.772) and Veterans’ Affairs Model (AUC = 0.740). These results were significantly better for predicting the presence of cancer than radiological features and artificial intelligence risk scores alone. Applying this classifier prospectively may lead to improved early lung cancer diagnosis and early treatment for patients with malignant nodules while sparing patients with benign entities from unnecessary and potentially harmful surgery. Clinical Trial Registration Number: ChiCTR1900026233, URL: http://www.chictr.org.cn/showproj.aspx?proj=43370.
AB - Lung cancer is the leading cause of cancer-related deaths worldwide and in China. Screening for lung cancer by low dose computed tomography (LDCT) can reduce mortality but has resulted in a dramatic rise in the incidence of indeterminate pulmonary nodules, which presents a major diagnostic challenge for clinicians regarding their underlying pathology and can lead to overdiagnosis. To address the significant gap in evaluating pulmonary nodules, we conducted a prospective study to develop a prediction model for individuals at intermediate to high risk of developing lung cancer. Univariate and multivariate logistic analyses were applied to the training cohort (n = 560) to develop an early lung cancer prediction model. The results indicated that a model integrating clinical characteristics (age and smoking history), radiological characteristics of pulmonary nodules (nodule diameter, nodule count, upper lobe location, malignant sign at the nodule edge, subsolid status), artificial intelligence analysis of LDCT data, and liquid biopsy achieved the best diagnostic performance in the training cohort (sensitivity 89.53%, specificity 81.31%, area under the curve [AUC] = 0.880). In the independent validation cohort (n = 168), this model had an AUC of 0.895, which was greater than that of the Mayo Clinic Model (AUC = 0.772) and Veterans’ Affairs Model (AUC = 0.740). These results were significantly better for predicting the presence of cancer than radiological features and artificial intelligence risk scores alone. Applying this classifier prospectively may lead to improved early lung cancer diagnosis and early treatment for patients with malignant nodules while sparing patients with benign entities from unnecessary and potentially harmful surgery. Clinical Trial Registration Number: ChiCTR1900026233, URL: http://www.chictr.org.cn/showproj.aspx?proj=43370.
KW - artificial intelligence
KW - early diagnosis
KW - liquid biopsy
KW - lung cancer
KW - prediction model
UR - http://www.scopus.com/inward/record.url?scp=85126823472&partnerID=8YFLogxK
U2 - 10.3389/fonc.2022.853801
DO - 10.3389/fonc.2022.853801
M3 - Article
AN - SCOPUS:85126823472
SN - 2234-943X
VL - 12
JO - Frontiers in Oncology
JF - Frontiers in Oncology
M1 - 853801
ER -