基于多参数和多区域放射组学特征的机器学习预测胶质母细胞瘤患者的放射治疗反应。

Behavioural Neurology Pub Date : 2020-10-24 eCollection Date: 2020-01-01 DOI:10.1155/2020/1712604
Zi-Qi Pan, Shu-Jun Zhang, Xiang-Lian Wang, Yu-Xin Jiao, Jian-Jian Qiu
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引用次数: 8

摘要

方法:对152例GBM患者的MRI影像、遗传资料及临床资料进行分析。来自TCIA数据集的122例患者(训练集:n = 82;验证集:n = 40)和30例来自地方医院的患者作为独立的检验数据集。从多参数MRI的多个区域提取放射组学特征。Kaplan-Meier生存分析用于验证影像学特征预测GBM患者术前放疗反应的能力。采用放射组学特征和术前临床危险因素的多因素Cox回归,进一步提高对GBM患者个体总生存期(OS)的预测能力,OS以nomogram形式呈现。结果:选取8个特征构建放射组学特征。TCIA组放射组学特征的c指数为0.703 (P < 0.001),独立检测组为0.757 (P = 0.001)。多因素Cox回归分析证实放射组学特征(HR: 0.290, P < 0.001)、年龄(HR: 1.023, P = 0.01)、KPS (HR: 0.968, P < 0.001)是GBM患者术前OS的独立危险因素。当放射组学特征和术前临床危险因素相结合时,放射组学nomogram进一步提高了个体患者OS预测的性能(TCIA队列和test队列的C-index分别为0.764和0.758)。结论:本研究建立的放射组学特征可以预测单个GBM患者对放疗的反应,可能是GBM精确放疗的新补充。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Machine Learning Based on a Multiparametric and Multiregional Radiomics Signature Predicts Radiotherapeutic Response in Patients with Glioblastoma.

Machine Learning Based on a Multiparametric and Multiregional Radiomics Signature Predicts Radiotherapeutic Response in Patients with Glioblastoma.

Machine Learning Based on a Multiparametric and Multiregional Radiomics Signature Predicts Radiotherapeutic Response in Patients with Glioblastoma.

Machine Learning Based on a Multiparametric and Multiregional Radiomics Signature Predicts Radiotherapeutic Response in Patients with Glioblastoma.

Methods: The MRI images, genetic data, and clinical data of 152 patients with GBM were analyzed. 122 patients from the TCIA dataset (training set: n = 82; validation set: n = 40) and 30 patients from local hospitals were used as an independent test dataset. Radiomics features were extracted from multiple regions of multiparameter MRI. Kaplan-Meier survival analysis was used to verify the ability of the imaging signature to predict the response of GBM patients to radiotherapy before an operation. Multivariate Cox regression including radiomics signature and preoperative clinical risk factors was used to further improve the ability to predict the overall survival (OS) of individual GBM patients, which was presented in the form of a nomogram.

Results: The radiomics signature was built by eight selected features. The C-index of the radiomics signature in the TCIA and independent test cohorts was 0.703 (P < 0.001) and 0.757 (P = 0.001), respectively. Multivariate Cox regression analysis confirmed that the radiomics signature (HR: 0.290, P < 0.001), age (HR: 1.023, P = 0.01), and KPS (HR: 0.968, P < 0.001) were independent risk factors for OS in GBM patients before surgery. When the radiomics signature and preoperative clinical risk factors were combined, the radiomics nomogram further improved the performance of OS prediction in individual patients (C-index = 0.764 and 0.758 in the TCIA and test cohorts, respectively).

Conclusion: This study developed a radiomics signature that can predict the response of individual GBM patients to radiotherapy and may be a new supplement for precise GBM radiotherapy.

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