首页> 外文期刊>AJNR. American journal of neuroradiology >Pretreatment ADC histogram analysis is a predictive imaging biomarker for bevacizumab treatment but not chemotherapy in recurrent glioblastoma
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Pretreatment ADC histogram analysis is a predictive imaging biomarker for bevacizumab treatment but not chemotherapy in recurrent glioblastoma

机译:预处理ADC直方图分析是贝伐单抗治疗而非复发性胶质母细胞瘤化疗的预测性成像生物标志物

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BACKGROUND AND PURPOSE: Pre-treatment ADC characteristics have been shown to predict response to bevacizumab in recurrent glioblastoma multiforme. However, no studies have examined whether ADC characteristics are specific to this particular treatment. The purpose of the current study was to determine whether ADC histogram analysis is a bevacizumab-specific or treatment- independent biomarker of treatment response in recurrent glioblastoma multiforme. MATERIALS AND METHODS: Eighty-nine bevacizumab-treated and 43 chemotherapy-treated recurrent glioblastoma multiformes never exposed to bevacizumab were included in this study. In all patients, ADC values in contrast-enhancing ROIs from MR imaging examinations performed at the time of recurrence, immediately before commencement of treatment for recurrence, were extracted and the resulting histogram was fitted to a mixed model with a double Gaussian distribution. Mean ADC in the lower Gaussian curve was used as the primary biomarker of interest. The Cox proportional hazards model and log-rank tests were used for survival analysis. RESULTS: Cox multivariate regression analysis accounting for the interaction between bevacizumab- and non-bevacizumab-treated patients suggested that the ability of the lower Gaussian curve to predict survival is dependent on treatment (progression-free survival, P = .045; overall survival, P = .003). Patients with bevacizumab-treated recurrent glioblastoma multiforme with a pretreatment lower Gaussian curve 1.2 μm2/ms had a significantly longer progression-free survival and overall survival compared with bevacizumab-treated patients with a lower Gaussian curve 1.2 μm2/ms. No differences in progression-free survival or overall survival were observed in the chemotherapy-treated cohort. Bevacizumab-treated patients with a mean lower Gaussian curve 1.2 μm2/ms had a significantly longer progression-free survival and overall survival compared with chemotherapy-treated patients. CONCLUSIONS: The mean lower Gaussian curve from ADC histogram analysis is a predictive imaging biomarker for bevacizumab-treated, not chemotherapy-treated, recurrent glioblastoma multiforme. Patients with recurrent glioblastoma multiforme with a mean lower Gaussian curve 1.2 μm2/ms have a survival advantage when treated with bevacizumab.
机译:背景与目的:预处理ADC的特性已显示可预测多形性胶质母细胞瘤复发中对贝伐单抗的反应。但是,没有研究检查ADC特性是否特定于此特定处理。本研究的目的是确定ADC直方图分析是多形性胶质母细胞瘤复发中贝伐单抗特异性或治疗依赖性生物标志物。材料与方法:本研究包括从未暴露于贝伐单抗的八十九种贝伐单抗治疗和43种化学疗法治疗的复发性胶质母细胞瘤多形体。在所有患者中,从复发时(即开始治疗复发之前)进行的MR成像检查中,在对比度增强的ROI中提取ADC值,并将直方图拟合为具有双高斯分布的混合模型。较低高斯曲线中的平均ADC被用作主要的生物标志物。使用Cox比例风险模型和对数秩检验进行生存分析。结果:Cox多元回归分析说明了贝伐单抗治疗和非贝伐单抗治疗患者之间的相互作用,这表明较低的高斯曲线预测生存的能力取决于治疗(无进展生存,P = .045;总体生存, P = 0.003)。与贝伐单抗治疗的复发性多形性胶质母细胞瘤患者相比,高贝斯曲线治疗的患者具有较低的高斯曲线(> 1.2μm2/ ms),其无进展生存期和总生存期明显高于低贝伐单抗治疗的高斯曲线<1.2μm2/ ms。在化疗治疗的队列中,无进展生存期或总生存期无差异。与化学疗法治疗的患者相比,贝伐单抗治疗的平均高斯曲线下限> 1.2μm2/ ms的患者的无进展生存期和总生存期明显更长。结论:ADC直方图分析的平均下高斯曲线是贝伐单抗治疗而不是化学治疗的复发性胶质母细胞瘤的预测性成像生物标志物。接受贝伐单抗治疗的多形性胶质母细胞瘤复发患者平均高斯曲线下限> 1.2μm2/ ms,具有生存优势。

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