中文版 | English
Title

CT-based radiomic phenotypes of lung adenocarcinoma: a preliminary comparative analysis with targeted next-generation sequencing

Author
Corresponding AuthorGong, Jingshan
Publication Years
2023-08-17
DOI
Source Title
EISSN
2296-858X
Volume10
Abstract
["Objectives: This study aimed to explore the relationship between computed tomography (CT)-based radiomic phenotypes and genomic profiles, including expression of programmed cell death-ligand 1 (PD-L1) and the 10 major genes, such as epidermal growth factor receptor (EGFR), tumor protein 53 (TP53), and Kirsten rat sarcoma viral oncogene (KRAS), in patients with lung adenocarcinoma (LUAD).","Methods: In total, 288 consecutive patients with pathologically confirmed LUAD were enrolled in this retrospective study. Radiomic features were extracted from preoperative CT images, and targeted genomic data were profiled through next-generation sequencing. PD-L1 expression was assessed by immunohistochemistry staining (chi-square test or Fisher's exact test for categorical data and the Kruskal-Wallis test for continuous data). A total of 1,013 radiomic features were obtained from each patient's CT images. Consensus clustering was used to cluster patients on the basis of radiomic features.","Results: The 288 patients were classified according to consensus clustering into four radiomic phenotypes: Cluster 1 (n = 11) involving mainly large solid masses with a maximum diameter of 5.1 +/- 2.0 cm; Clusters 2 and 3 involving mainly part-solid and solid masses with maximum diameters of 2.1 +/- 1.4 cm and 2.1 +/- 0.9 cm, respectively; and Cluster 4 involving mostly small ground-glass opacity lesions with amaximumdiameter of 1.0 +/- 0.9 cm. Di erences inmaximum diameter, PD-L1 expression, and TP53, EGFR, BRAF, ROS1, and ERBB2 mutations among the four clusters were statistically significant. Regarding targeted therapy and immunotherapy, EGFR mutations were highest in Cluster 2 (73.1%); PD-L1 expression was highest in Cluster 1 (45.5%).","Conclusion: Our findings provide evidence that CT-based radiomic phenotypes could non-invasively identify LUADs with di erent molecular characteristics, showing the potential to provide personalized treatment decision-making support for LUAD patients."]
Keywords
URL[Source Record]
Indexed By
Language
English
SUSTech Authorship
Corresponding
Funding Project
null[82172026]
WOS Research Area
General & Internal Medicine
WOS Subject
Medicine, General & Internal
WOS Accession No
WOS:001058948200001
Publisher
Data Source
Web of Science
Citation statistics
Cited Times [WOS]:0
Document TypeJournal Article
Identifierhttp://kc.sustech.edu.cn/handle/2SGJ60CL/571815
DepartmentShenzhen People's Hospital
Affiliation
1.Jinan Univ, Clin Med Coll 2, Shenzhen, Peoples R China
2.Jinan Univ, Southern Univ Sci & Technol, Shenzhen Peoples Hosp, Clin Med Coll 2,Affiliated Hosp 1,Dept Radiol, Shenzhen, Peoples R China
3.Jinan Univ, Guangzhou Red Cross Hosp, Guangzhou, Guangdong, Peoples R China
Corresponding Author AffilicationShenzhen People's Hospital
Recommended Citation
GB/T 7714
Liu, Xiaowen,Xu, Ting,Wang, Shuxing,et al. CT-based radiomic phenotypes of lung adenocarcinoma: a preliminary comparative analysis with targeted next-generation sequencing[J]. FRONTIERS IN MEDICINE,2023,10.
APA
Liu, Xiaowen.,Xu, Ting.,Wang, Shuxing.,Chen, Yaxi.,Jiang, Changsi.,...&Gong, Jingshan.(2023).CT-based radiomic phenotypes of lung adenocarcinoma: a preliminary comparative analysis with targeted next-generation sequencing.FRONTIERS IN MEDICINE,10.
MLA
Liu, Xiaowen,et al."CT-based radiomic phenotypes of lung adenocarcinoma: a preliminary comparative analysis with targeted next-generation sequencing".FRONTIERS IN MEDICINE 10(2023).
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