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治疗前 ADC 直方图分析是预测贝伐珠单抗治疗而非化疗治疗复发性胶质母细胞瘤的影像学生物标志物。

Pretreatment ADC histogram analysis is a predictive imaging biomarker for bevacizumab treatment but not chemotherapy in recurrent glioblastoma.

机构信息

From the Departments of Radiological Sciences (B.M.E., H.J.K., W.B.P., R.J.H., D.C.W.).

出版信息

AJNR Am J Neuroradiol. 2014 Apr;35(4):673-9. doi: 10.3174/ajnr.A3748. Epub 2013 Oct 17.

Abstract

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 μm(2)/ms had a significantly longer progression-free survival and overall survival compared with bevacizumab-treated patients with a lower Gaussian curve < 1.2 μm(2)/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 μm(2)/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 μm(2)/ms have a survival advantage when treated with bevacizumab.

摘要

背景与目的

术前 ADC 特征已被证实可预测复发性多形性胶质母细胞瘤对贝伐珠单抗的反应。然而,尚无研究探讨 ADC 特征是否是针对该特定治疗的特异性特征。本研究旨在确定 ADC 直方图分析是否是复发性多形性胶质母细胞瘤中贝伐珠单抗特异性或治疗独立性的治疗反应生物标志物。

材料与方法

本研究纳入了 89 例接受贝伐珠单抗治疗和 43 例从未接受过贝伐珠单抗化疗的复发性多形性胶质母细胞瘤患者。在所有患者中,均从复发性疾病时、治疗复发性疾病前即刻进行的 MRI 检查的增强 ROI 中提取 ADC 值,并对得到的直方图进行拟合,采用双高斯分布的混合模型。下高斯曲线的平均 ADC 用作主要感兴趣的生物标志物。采用 Cox 比例风险模型和对数秩检验进行生存分析。

结果

在考虑贝伐珠单抗治疗和非贝伐珠单抗治疗患者之间相互作用的 Cox 多变量回归分析中,下高斯曲线预测生存的能力取决于治疗(无进展生存期,P =.045;总生存期,P =.003)。贝伐珠单抗治疗的复发性多形性胶质母细胞瘤患者,治疗前下高斯曲线>1.2μm2/ms,其无进展生存期和总生存期明显长于下高斯曲线<1.2μm2/ms的贝伐珠单抗治疗患者。在化疗治疗组中,无进展生存期或总生存期无差异。贝伐珠单抗治疗的下高斯曲线>1.2μm2/ms 的患者,其无进展生存期和总生存期明显长于化疗治疗的患者。

结论

ADC 直方图分析的下高斯曲线平均值是贝伐珠单抗治疗而非化疗治疗的复发性多形性胶质母细胞瘤的预测性成像生物标志物。复发性多形性胶质母细胞瘤患者的下高斯曲线平均值>1.2μm2/ms 时,接受贝伐珠单抗治疗的生存获益。

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