A Radiomics Model for Predicting the Response to Bevacizumab in Brain Necrosis after Radiotherapy

被引:35
作者
Cai, Jinhua [1 ]
Zheng, Junjiong [2 ]
Shen, Jun [3 ]
Yuan, Zhiyong [4 ,5 ]
Xie, Mingwei [3 ]
Gao, Miaomiao [4 ,5 ]
Tan, Hongqi [6 ]
Liang, Zhongguo [6 ,7 ]
Rong, Xiaoming [1 ]
Li, Yi [1 ]
Li, Honghong [1 ]
Jiang, Jingru [1 ]
Zhao, Huiying [8 ,9 ]
Argyriou, Andreas A. [10 ]
Chua, Melvin L. K. [6 ,11 ,12 ]
Tang, Yamei [1 ,9 ,13 ]
机构
[1] Sun Yat Sen Univ, Dept Neurol, Bioland Lab, Sun Yat Sen Mem Hosp, Guangzhou, Peoples R China
[2] Sun Yat Sen Univ, Dept Urol, Sun Yat Sen Mem Hosp, Guangzhou, Peoples R China
[3] Sun Yat Sen Univ, Sun Yat Sen Mem Hosp, Dept Radiol, Guangzhou, Peoples R China
[4] Tianjin Med Univ Canc Inst & Hosp, Natl Clin Res Ctr Canc Key Lab Canc Prevent & The, Dept Radiotherapy, Tianjin, Peoples R China
[5] Tianjins Clin Res Ctr Canc, Tianjin, Peoples R China
[6] Natl Canc Ctr Singapore, Div Radiat Oncol, Singapore, Singapore
[7] Guangxi Med Univ, Affiliated Tumor Hosp, Nanning, Guangxi, Peoples R China
[8] Sun Yat Sen Univ, Med Res Ctr, Sun Yat Sen Mem Hosp, Guangzhou, Peoples R China
[9] Sun Yat Sen Univ, Sun Yat Sen Mem Hosp, Guangdong Prov Key Lab Malignant Tumor Epigenet &, Guangzhou, Peoples R China
[10] St Andrews State Gen Hosp Patras, Patras, Greece
[11] Natl Canc Ctr Singapore, Div Med Sci, Singapore, Singapore
[12] Duke Natl Univ Singapore Med Sch, Oncol Acad Program, Singapore, Singapore
[13] Sun Yat Sen Univ, Zhongshan Sch Med, Guangdong Prov Key Lab Brain Funct & Dis, Guangzhou, Peoples R China
基金
英国医学研究理事会; 国家重点研发计划; 新加坡国家研究基金会; 中国国家自然科学基金;
关键词
CEREBRAL RADIATION NECROSIS; CENTRAL-NERVOUS-SYSTEM; DIAGNOSIS; THERAPY; CHEMOTHERAPY; MECHANISMS; METASTASES; MANAGEMENT; FEATURES;
D O I
10.1158/1078-0432.CCR-20-1264
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Bevacizumab is considered a promising therapy for brain necrosis after radiotherapy, while some patients fail to derive benefit or even worsen. Hence, we developed and validated a radiomics model for predicting the response to bevacizumab in patients with brain necrosis after radiotherapy. Experimental Design: A total of 149 patients (with 194 brain lesions; 101, 51, and 42 in the training, internal, and external validation sets, respectively) receiving bevacizumab were enrolled. In total, 1,301 radiomic features were extracted from the pretreatment MRI images of each lesion. In the training set, a radiomics signature was constructed using the least absolute shrinkage and selection operator algorithm. Multivariable logistic regression analysis was then used to develop a radiomics model incorporated in the radiomics signature and independent clinical predictors. The performance of the model was assessed by its discrimination, calibration, and clinical usefulness with internal and external validation. Results: The radiomics signature consisted of 18 selected features and showed good discrimination performance. The model, which integrates the radiomics signature, the interval between radiotherapy and diagnosis of brain necrosis, and the interval between diagnosis of brain necrosis and treatment with bevacizumab, showed favorable calibration and discrimination in the training set (AUC 0.916). These findings were confirmed in the validation sets (AUC 0.912 and 0.827, respectively). Decision curve analysis confirmed the clinical utility of the model. Conclusions: The presented radiomics model, available as an online calculator, can serve as a user-friendly tool for individualized prediction of the response to bevacizumab in patients with brain necrosis after radiotherapy.
引用
收藏
页码:5438 / 5447
页数:10
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