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Lung adenocarcinoma: development of nomograms based on PET/CT images for prediction of epidermal growth factor receptor mutation status and subtypes | |
Huang, Lele1,2,3,4,5; Cao, Yuntai6; Zhou, Fei7; Li, Jicheng2,8; Ren, Jialiang9; Zhang, Guojin10; Luo, Yongjun1,2,3,4,5; Liu, Jiangyan2,4,5; He, Jiangping11; Zhou, Junlin1,4,5 | |
2022-03 | |
发表期刊 | NUCLEAR MEDICINE COMMUNICATIONS |
卷号 | 43期号:3页码:310-322 |
摘要 | Objective To develop nomograms that combine clinical characteristics, computed tomographic (CT) features and F-18-fluorodeoxyglucose PET (F-18-FDG PET) metabolic parameters for individual prediction of epidermal growth factor receptor (EGFR) mutation status and exon 19 deletion mutation and exon 21 point mutation (21 L858R) subtypes in lung adenocarcinoma. Methods In total 124 lung adenocarcinoma patients who underwent EGFR mutation testing and whole-body F-18-FDG PET/CT were enrolled. Each patient's clinical characteristics (age, sex, smoking history, etc.), CT features (size, location, margins, etc.) and four metabolic parameters (SUVmax, SUVmean, MTV and TLG) were recorded and analyzed. Logistic regression analyses were performed to screen for significant predictors of EGFR mutation status and subtypes, and these predictors were presented as easy-to-use nomograms. Results According to the results of multiple regression analysis, three nomograms for individualized prediction of EGFR mutation status and subtypes were constructed. The area under curve values of three nomograms were 0.852 (95% CI, 0.783-0.920), 0.857 (95% CI, 0.778-0.937) and 0.893 (95% CI, 0.819-0.968) of EGFR mutation vs. wild-type, 19 deletion mutation vs. wild-type and 21 L858R vs. wild-type, respectively. Only calcification showed significant differences between the EGFR 19 deletion and 21 L858R mutations. Conclusion EGFR 21 L858R mutation was more likely to be nonsolid texture with air bronchograms and pleural retraction on CT images. And they were more likely to be associated with lower FDG metabolic activity compared with those wild-types. The sex difference was mainly caused by the 19 deletion mutation, and calcification was more frequent in them. |
关键词 | F-18-FDG PET CT epidermal growth factor receptor lung adenocarcinoma mutation nomogram |
DOI | 10.1097/MNM.0000000000001519 |
收录类别 | SCIE |
ISSN | 0143-3636 |
语种 | 英语 |
WOS研究方向 | Radiology, Nuclear Medicine & Medical Imaging |
WOS类目 | Radiology, Nuclear Medicine & Medical Imaging |
WOS记录号 | WOS:000753310600009 |
出版者 | LIPPINCOTT WILLIAMS & WILKINS |
原始文献类型 | Article |
EISSN | 1473-5628 |
引用统计 | |
文献类型 | 期刊论文 |
条目标识符 | http://ir.lzufe.edu.cn/handle/39EH0E1M/32024 |
专题 | 信息工程与人工智能学院 |
作者单位 | 1.Lanzhou Univ, Hosp 2, Dept Radiol, Cuiyingmen 82, Lanzhou 730030, Peoples R China; 2.Lanzhou Univ, Hosp 2, Dept Nucl Med, Lanzhou, Peoples R China; 3.Lanzhou Univ, Clin Sch 2, Lanzhou, Peoples R China; 4.Key Lab Med Imaging Gansu Prov, Lanzhou, Peoples R China; 5.Gansu Int Sci & Technol Cooperat Base Med Imaging, Lanzhou, Peoples R China; 6.Qinghai Univ, Affiliated Hosp, Dept Radiol, Xining, Peoples R China; 7.Gansu Univ Chinese Med, Sch Informat Sci & Engn, Lanzhou, Peoples R China; 8.Lanzhou Univ, Sch Publ Hlth, Lanzhou, Peoples R China; 9.GE Healthcare, Dept Pharmaceut Diag, Beijing, Peoples R China; 10.Sichuan Acad Med Sci, Sichuan Prov Peoples Hosp, Chengdu, Peoples R China; |
推荐引用方式 GB/T 7714 | Huang, Lele,Cao, Yuntai,Zhou, Fei,et al. Lung adenocarcinoma: development of nomograms based on PET/CT images for prediction of epidermal growth factor receptor mutation status and subtypes[J]. NUCLEAR MEDICINE COMMUNICATIONS,2022,43(3):310-322. |
APA | Huang, Lele.,Cao, Yuntai.,Zhou, Fei.,Li, Jicheng.,Ren, Jialiang.,...&Zhou, Junlin.(2022).Lung adenocarcinoma: development of nomograms based on PET/CT images for prediction of epidermal growth factor receptor mutation status and subtypes.NUCLEAR MEDICINE COMMUNICATIONS,43(3),310-322. |
MLA | Huang, Lele,et al."Lung adenocarcinoma: development of nomograms based on PET/CT images for prediction of epidermal growth factor receptor mutation status and subtypes".NUCLEAR MEDICINE COMMUNICATIONS 43.3(2022):310-322. |
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