Apparent diffusion coefficient histogram analysis stratifies progression-free and overall survival in patients with recurrent GBM treated with bevacizumab: a multi-center study.

Apparent diffusion coefficient histogram analysis stratifies progression-free and overall survival in patients with recurrent GBM treated with bevacizumab: a multi-center study.
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DOI:
10.1007/s11060-012-0847-y
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发表时间:
2012-07
影响因子:
3.9
通讯作者:
Cloughesy, Timothy
Cloughesy, Timothy
中科院分区:
医学2区
文献类型:
--
作者:
Pope, Whitney B.;Qiao, Xin Joe;Kim, Hyun J.;Lai, Albert;Nghiemphu, Phioanh;Xue, Xi;Ellingson, Benjamin M.;Schiff, David;Aregawi, Dawit;Cha, Soonmee;Puduvalli, Vinay K.;Wu, Jing;Yung, Wai-Kwan A.;Young, Geoffrey S.;Vredenburgh, James;Barboriak, Dan;Abrey, Lauren E.;Mikkelsen, Tom;Jain, Rajan;Paleologos, Nina A.;Lada, Patricia;Prados, Michael;Goldin, Jonathan;Wen, Patrick Y.;Cloughesy, Timothy

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我们在多中心 BRAIN 研究中测试了表观扩散系数 (ADC) 直方图分析对贝伐珠单抗治疗的复发性多形性胶质母细胞瘤 (GBM) 患者的无进展生存期 (PFS) 和总生存期 (OS) 分层的预测价值。通过从拟合两条正态分布混合曲线的 T1 加权后对比图像上的增强肿瘤区域生成 ADC 直方图,对参加 BRAIN 研究的患者 (n = 97) 的可用 MRI 进行检查。使用 Cox 比例风险比和带对数秩检验的 Kaplan-Meier 方法,测试了 ADC 分类器(包括下曲线平均 ADC (ADC-L) 和平均下曲线比例 (LCP))对 PFS 和 OS 进行分层的能力。平均 ADC-L 为 1,209 × 10−6mm2/s ± 224 (SD),平均 LCP 为 0.71 ± 0.23 (SD)。低 ADC-L 与较差的结果相关。 ADC-L 低于平均值与高于平均值的患者的 6 个月 PFS、总体 PFS 和 OS 的风险比分别为 3.1(95% 置信区间:1.6, 6.1;P = 0.001)、2.3(95% CI:1.3、4.0;P = 0.002)和 2.4(95% CI:1.4、4.2;P = 0.002),分别。在 ADC-L<1,209 且 LCP>0.71 的患者中,与 ADC-L>1,209 且 LCP <0.71 的患者相比,中位进展时间缩短了 2.28 倍,中位 OS 降低了 1.42 倍。 ADC 直方图分析的预测价值(其中低 ADC-L 与不良预后相关)在多中心 (BRAIN) 研究的事后分析中在接受贝伐珠单抗治疗的复发性 GBM 患者中得到证实。
We have tested the predictive value of apparent diffusion coefficient (ADC) histogram analysis in stratifying progression-free survival (PFS) and overall survival (OS) in bevacizumab-treated patients with recurrent glioblastoma multiforme (GBM) from the multi-center BRAIN study. Available MRI’s from patients enrolled in the BRAIN study (n = 97) were examined by generating ADC histograms from areas of enhancing tumor on T1 weighted post-contrast images fitted to a two normal distribution mixture curve. ADC classifiers including the mean ADC from the lower curve (ADC-L) and the mean lower curve proportion (LCP) were tested for their ability to stratify PFS and OS by using Cox proportional hazard ratios and the Kaplan–Meier method with log-rank test. Mean ADC-L was 1,209 × 10−6mm2/s ± 224 (SD), and mean LCP was 0.71 ± 0.23 (SD). Low ADC-L was associated with worse outcome. The hazard ratios for 6-month PFS, overall PFS, and OS in patients with less versus greater than mean ADC-L were 3.1 (95 % confidence interval: 1.6, 6.1; P = 0.001), 2.3 (95 % CI: 1.3, 4.0; P = 0.002), and 2.4 (95 % CI: 1.4, 4.2; P = 0.002), respectively. In patients with ADC-L<1,209 and LCP>0.71 versus ADC-L>1,209 and LCP <0.71, there was a 2.28-fold reduction in the median time to progression, and a 1.42-fold decrease in the median OS. The predictive value of ADC histogram analysis, in which low ADC-L was associated with poor outcome, was confirmed in bevacizumab-treated patients with recurrent GBM in a post hoc analysis from the multi-center (BRAIN) study.
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