首页> 美国卫生研究院文献>Neuro-Oncology >NIMG-54. DIFFUSION MRI PHENOTYPES PREDICT OVERALL SURVIVAL BENEFIT FROM BEVACIZUMAB IN RECURRENT GLIOBLASTOMA WITH A LARGE TUMOR BURDEN: EVIDENCE FROM CLINICAL PRACTICE AND A MULTICENTER PHASE 3 TRIAL
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NIMG-54. DIFFUSION MRI PHENOTYPES PREDICT OVERALL SURVIVAL BENEFIT FROM BEVACIZUMAB IN RECURRENT GLIOBLASTOMA WITH A LARGE TUMOR BURDEN: EVIDENCE FROM CLINICAL PRACTICE AND A MULTICENTER PHASE 3 TRIAL

机译:nimg-54。扩散MRI表型预测北伐木母细胞瘤中的总生存益处具有大的肿瘤负担:来自临床实践的证据和多中心3阶段试验

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摘要

We have previously shown that diffusion MR characteristics are a predictive imaging biomarker for survival benefit in recurrent glioblastoma treated with anti-VEGF therapy; however, contemporary clinical use of bevacizumab is often limited to patients with very large tumors and/or after multiple recurrences. We hypothesize that diffusion MR characteristics can be used to predict long-term survival benefit in these patients, which may be beneficial for clinical decision-making. The current study identified 83 recurrent glioblastoma patients from our institution who were treated with bevacizumab over the past 5 years with high quality anatomic and diffusion MRI data. Of these 83 patients, 35 had large contrast enhancing tumors (>20cc or >3.4cm diameter, group average). Additionally, we identified 37 recurrent glioblastoma patients from the bevacizumab treated control arm of a recent multicenter phase III trial ({"type":"clinical-trial","attrs":{"text":"NCT02511405","term_id":"NCT02511405"}}NCT02511405) with high quality data and large enhancing tumors for validation. Pre-treatment tumor volume was quantified using T1 subtraction maps and apparent diffusion coefficient (ADC) histogram analysis was used to phenotype patients as having high (> 1.24 um2/ms) or low (< 1.24 um2/ms) ADCL, the mean value of the lower peak using a double Gaussian mixed model. Median overall survival in patients with large volume recurrent glioblastoma was ~5.7 months. High ADCL was associated with significantly longer overall survival (OS) compared with low ADCL in both single center (P=0.0271, HR=0.486, mOS=5.5 vs. 2.8mo) and multicenter phase III data (P=0.0457, HR=0.507, mOS=7.9 vs. 5.7mo). Accounting for absolute tumor volume and age, both cohorts showed that ADCL was an independent prognostic factor for OS (Cox, P< 0.01). In summary, pre-treatment diffusion MR imaging is an independent predictive biomarker for OS in recurrent glioblastoma with a large tumor burden.
机译:我们之前已经表明,扩散MR特性是预测成像生物标志物,用于用抗VEGF治疗治疗的复发胶质母细胞瘤中的存活益处;然而,当代临床用途贝伐单抗通常限于肿瘤非常大的患者和/或多重复发后。我们假设扩散MR特性可用于预测这些患者的长期存活益处,这可能对临床决策有益。目前的研究确定了我们的机构的83名经常性胶质母细胞瘤患者,在过去的5年里用贝伐单抗治疗,高品质解剖和扩散MRI数据。在这83名患者中,35例具有大的对比增强肿瘤(> 20cc或3.4cm直径,群体平均值)。此外,我们鉴定了来自最近多中心阶段III试验的Bevacizumab处理的控制臂的37例复制胶质母细胞瘤患者({“型”:“临床试验”,“attrs”:{“text”:“nct02511405”,“term_id”: “NCT02511405”}} NCT02511405)具有高质量数据和大型增强肿瘤进行验证。使用T1减法图定量预处理肿瘤体积,并且表观扩散系数(ADC)直方图分析用于表型患者,其具有高(> 1.24MU2 / MS)或低(<1.24MU2 / MS)ADCL,平均值使用双高斯混合模型的较低峰。大量复发性胶质母细胞瘤患者中位的整体生存率为约5.7个月。与单一中心的低AdCl相比,高AdCl与显着更长的总存活(OS)相关联(P = 0.0271,HR = 0.486,MOS = 5.5 Vs.28MO)和多中心III数据(P = 0.0457,HR = 0.507 ,mos = 7.9与5.7mo)。对绝对肿瘤的体积和年龄核算,两者都表明AdCl是OS的独立预后因子(COX,P <0.01)。总之,预处理扩散MR成像是一种独立于肿瘤负担的复发胶质母细胞瘤的OS的独立预测生物标志物。

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