Radiogenomic associations clear cell renal cell carcinoma: an exploratory study

被引:2
|
作者
Liu, Derek H. [1 ]
Dani, Komal A. [1 ]
Reddy, Sharath S. [1 ]
Lei, Xiaomeng [2 ]
Demirjian, Natalie L. [2 ]
Hwang, Darryl H. [2 ]
Varghese, Bino A. [2 ,11 ]
Rhie, Suhn K. [3 ]
Yap, Felix Y. [10 ]
Quinn, David I. [5 ]
Siddiqi, Imran [6 ]
Aron, Manju [6 ]
Vaishampayan, Ulka [7 ]
Zahoor, Haris
Cen, Steven Y. [2 ,8 ]
Gill, Inderbir S. [4 ]
Duddalwar, Vinay A. [2 ,4 ,9 ]
机构
[1] Univ Southern Calif, Keck Sch Med, Los Angeles, CA 90033 USA
[2] Univ Southern Calif, Keck Sch Med, Dept Radiol, Los Angeles, CA 90033 USA
[3] Univ Southern Calif, Dept Biochem & Mol Med, Los Angeles, CA 90033 USA
[4] Univ Southern Calif, Inst Urol, Los Angeles, CA 90033 USA
[5] Univ Southern Calif, Dept Med, Los Angeles, CA 90033 USA
[6] Univ Southern Calif, Dept Pathol, Los Angeles, CA 90033 USA
[7] Univ Michigan, Dept Med, Ann Arbor, MI 48109 USA
[8] Univ Southern Calif, Dept Neurol, Los Angeles, CA 90033 USA
[9] Univ Southern Calif, Dept Biomed Engn, Los Angeles, CA 90089 USA
[10] Radiol Associates San Luis Obispo, Atascadero, CA USA
[11] Univ Southern Calif, Dept Radiol, USC Norris Comprehens Canc & Hosp, Keck Sch Med, 1441 Eastlake Ave, Los Angeles, CA 90033 USA
关键词
CANCER; SETD2; PBRM1; EXPRESSION; REGRESSION; THERAPIES; BIOMARKER; JARID1C; BAP1;
D O I
10.1159/000530719
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
OBJECTIVES: This study investigates how quantitative texture analysis can be used to non-invasively identify novel radiogenomic correlations with Clear Cell Renal Cell Carcinoma (ccRCC) biomarkers. METHODS: The Cancer Genome Atlas-Kidney Renal Clear Cell Carcinoma (TCGA-KIRC) open-source database was used to identify 190 sets of patient genomic data that had corresponding multiphase contrast-enhanced CT images in The Cancer Imaging Archive (TCIA-KIRC). 2824 radiomic features spanning fifteen texture families were extracted from CT images using a custom-built MATLAB software package. Robust radiomic features with strong inter-scanner reproducibility were selected. Random Forest (RF), AdaBoost, and Elastic Net machine learning (ML) algorithms evaluated the ability of the selected radiomic features to predict the presence of 12 clinically relevant molecular biomarkers identified from literature. ML analysis was repeated with cases stratified by stage (I/II vs. III/IV) and grade (1/2 vs. 3/4). 10-fold cross validation was used to evaluate model performance. RESULTS: Before stratification by tumor grade and stage, radiomics predicted the presence of several biomarkers with weak discrimination (AUC 0.60-0.68). Once stratified, radiomics predicted KDM5C, SETD2, PBRM1, and mTOR mutation status with acceptable to excellent predictive discrimination (AUC ranges from 0.70 to 0.86). CONCLUSIONS: Radiomic texture analysis can potentially identify a variety of clinically relevant biomarkers in patients with ccRCC and may have a prognostic implication.
引用
收藏
页码:375 / 388
页数:14
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