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首页> 外文期刊>Frontiers in Oncology >CT-Based Radiomic Signature as a Prognostic Factor in Stage IV ALK-Positive Non-small-cell Lung Cancer Treated With TKI Crizotinib: A Proof-of-Concept Study
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CT-Based Radiomic Signature as a Prognostic Factor in Stage IV ALK-Positive Non-small-cell Lung Cancer Treated With TKI Crizotinib: A Proof-of-Concept Study

机译:基于CT的辐射症作为阶段IV中的预后因子<斜斜体> ALK - 用TKI CRIZOTINIB治疗的阳性非小细胞肺癌:概念证明研究

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摘要

Objectives: To identify a computed tomography (CT)-based radiomic signature for predicting progression-free survival (PFS) in stage IV anaplastic lymphoma kinase ( ALK )-positive non-small-cell lung cancer (NSCLC) patients treated with tyrosine kinase inhibitor (TKI) crizotinib. Materials and Methods: This retrospective proof-of-concept study included a cohort of 63 stage IV ALK -positive NSCLC patients who had received TKI crizotinib therapy for model construction and validation. Another independent cohort including 105 stage IV EGFR -positive NSCLC patients was also used for external validation in EGFR -TKI treatment. We initially extracted 481 quantitative three-dimensional features derived from manually segmented tumor volumes of interest. Pearson's correlation analysis along with the least absolute shrinkage and selection operator (LASSO) penalized Cox proportional hazards regression was successively performed to select critical radiomic features. A CT-based radiomic signature for PFS prediction was obtained using multivariate Cox regression. The performance evaluation of the radiomic signature was conducted using the concordance index (C-index), time-dependent receiver operating characteristic (ROC) analysis, and Kaplan–Meier survival analysis. Results: A radiomic signature containing three features showed significant prognostic performance for ALK -positive NSCLC patients in both the training cohort (C-index, 0.744; time-dependent AUC, 0.895) and the validation cohort (C-index, 0.717; time-dependent AUC, 0.824). The radiomic signature could significantly risk-stratify ALK -positive NSCLC patients (hazard ratio, 2.181; P & 0.001) and outperformed other prognostic factors. However, no significant association with PFS was captured for the radiomic signature in the EGFR -positive NSCLC cohort (log-rank tests, P = 0.41). Conclusions: The CT-based radiomic features can capture valuable information regarding the tumor phenotype. The proposed radiomic signature was found to be an effective prognostic factor in stage IV ALK mutated nonsynchronous nodules in NSCLC patients treated with a TKI.
机译:目的:鉴定计算的断层摄影(CT)的辐射染色签名,用于预测IV阶段的无流动性淋巴瘤激酶(ALK)阳性非小细胞肺癌(NSCLC)患者的无进展存活(PFS)患者(TKI)CRIZOTINIB。材料和方法:该回顾性概念证据包括群组群体Ⅳ期Ⅳ期持续的核心系列患者,接受了TKI Crizotinib治疗的模型建设和验证。另一种独立的群组包括105阶段EGFR - 阳性NSCLC患者也用于EGFR -TKI治疗中的外部验证。我们首先提取了从手动分段的肿瘤体积源自感兴趣的481种定量三维特征。 Pearson的相关性分析以及绝对的收缩和选择操作员(套索)惩罚的Cox比例危险回归是连续进行的,以选择临界辐射特征。使用多元COX回归获得PFS预测的基于CT基的射谱签名。使用齐全指数(C折射率),时间依赖的接收器操作特征(ROC)分析和Kaplan-Meier生存分析进行了射致签名的性能评估。结果:含有三种特征的辐射瘤特征对于培训队列(C折射率,0.744;时间依赖性AUC,0.895)和验证队列(C折射率,0.717;时间 - 依赖AUC,0.824)。射致签名可以显着风险 - 分层alk阳性NSCLC患者(危险比,2.181; p <0.001),并且优于其他预后因素。然而,在EGFR - 阳性NSCLC队列中的辐射瘤签名没有显着关联与PFS(对数级测试,P = 0.41)。结论:基于CT基的射域特征可以捕获有关肿瘤表型的有价值的信息。发现所提出的辐射素签名是在用TKI处理的NSCLC患者中阶段IV Alk突变的不同步结节中的有效预后因子。

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