A Quantitative CT Imaging Signature Predicts Survival and Complements Established Prognosticators in Stage I Non-Small Cell Lung Cancer

医学 危险系数 阶段(地层学) 基因签名 肿瘤科 比例危险模型 队列 内科学 肺癌 癌症 代理终结点 置信区间 基因表达 基因 生物 古生物学 化学 生物化学
作者
Juheon Lee,Bailiang Li,Yi Cui,Xiaoli Sun,Jia Wu,Hui Zhu,Jinming Yu,Michael F. Gensheimer,Billy W. Loo,Maximilian Diehn,Ruijiang Li
出处
期刊:International Journal of Radiation Oncology Biology Physics [Elsevier]
卷期号:102 (4): 1098-1106 被引量:22
标识
DOI:10.1016/j.ijrobp.2018.01.006
摘要

Purpose

Prognostic biomarkers are needed to guide the management of early-stage non-small cell lung cancer (NSCLC). This work aims to develop an image-based prognostic signature and assess its complementary value to existing biomarkers.

Methods and Materials

We retrospectively analyzed data of stage I NSCLC in 8 cohorts. On the basis of an analysis of 39 computed tomography (CT) features characterizing tumor and its relation to neighboring pleura, we developed a prognostic signature in an institutional cohort (n = 117) and tested it in an external cohort (n = 88). A third cohort of 89 patients with CT and gene expression data was used to create a surrogate genomic signature of the imaging signature. We conducted further validation using data from 5 gene expression cohorts (n = 639) and built a composite signature by integrating with the cell-cycle progression (CCP) score and clinical variables.

Results

An imaging signature consisting of a pleural contact index and normalized inverse difference was significantly associated with overall survival in both imaging cohorts (P = .0005 and P = .0009). Functional enrichment analysis revealed that genes highly correlated with the imaging signature were related to immune response, such as lymphocyte activation and chemotaxis (false discovery rate < 0.05). A genomic surrogate of the imaging signature remained a significant predictor of survival when we adjusted for known prognostic factors (hazard ratio, 1.81; 95% confidence interval, 1.34-2.44; P < .0001) and stratified patients within subgroups as defined by stage, histology, or CCP score. A composite signature outperformed the genomic surrogate, CCP score, and clinical model alone (P < .01) regarding concordance index (0.70 vs 0.62-0.63).

Conclusions

The proposed CT imaging signature reflects fundamental biological differences in tumors and predicts overall survival in patients with stage I NSCLC. When combined with established prognosticators, the imaging signature improves survival prediction.

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