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首页> 外文期刊>Journal of Neuro-Oncology >Imaging response criteria for recurrent gliomas treated with bevacizumab: Role of diffusion weighted imaging as an imaging biomarker
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Imaging response criteria for recurrent gliomas treated with bevacizumab: Role of diffusion weighted imaging as an imaging biomarker

机译:贝伐单抗治疗复发性神经胶质瘤的影像学反应标准:弥散加权成像作为影像学生物标志物的作用

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The purpose of this study was to assess the usefulness of diffusion weighted imaging as an additional imaging biomarker for treatment response in recurrent/progressive malignant gliomas treated with bevacizumab alone or in combination with other chemotherapeutic agents. Twenty patients treated with bevacizumab alone or concurrent chemotherapy were followed up with serial MR imaging. Volume and ADC values of contrast enhancing lesion (CELvol, CELADC) and also of non-enhancing lesion (NELvol, NELADC) were obtained. CELvol showed a progressive decrease in non-progressors with a median percentage change of −73.2% (P = 0.001) as compared to −33.4% for progressors by 1 year/last imaging (P = 0.382). NELvol also showed a decrease in non-progressors on follow up imaging though only significant for 3 months follow up (P = 0.042). In progressors, CELvol and NELvol showed initial decrease followed by slight increase by 1 year/last imaging though not significant (P value of 0.382 and 0.46, respectively). CELADC and NELADC in non-progressors did not show any statistically significant change though there was slight trend for positive percent change especially for CELADC by 1 year/last imaging follow up study (P value of 0.077 and 0.339, respectively). Progressors showed a progressive negative percent change of CELADC and NELADC. In progressors, NELADC decreased at 6 weeks (P = 0.054), 3 months (P = 0.023) and 1 year/last (P = 0.078) as compared to baseline study and was also statistically significant as compared to non-progressors at 6 weeks (P = 0.047) and 3 months (P = 0.025). CELADC and NELADC appear to follow different trends over time for non-progressors and progressors with a stable to slightly progressive increase in non-progressors and a progressive decrease in progressors, especially early on. These findings suggest that DWI may be used as an additional imaging biomarker for early treatment response. Keywords Diffusion - ADC - Avastin - Bevacizumab - Recurrent glioma
机译:这项研究的目的是评估弥散加权成像作为单独使用贝伐单抗或与其他化疗药物联合治疗的复发/进行性恶性神经胶质瘤的治疗反应的附加成像生物标志物的有用性。接受贝伐单抗单独治疗或同期化疗的20例患者接受了连续MR成像随访。对比增强病变(CEL vol ,CEL ADC )和非增强病变(NEL vol ,NEL ADC )。 CEL vol 显示非进展者逐渐减少,中位值变化百分比为-73.2%(P = 0.001),相比于经过1年/最后一次成像的进展者为-33.4%(P = 0.382) 。 NEL vol 在随访影像学中也显示出非进展的减少,尽管随访3个月才显着(P = 0.042)。在进展者中,CEL vol 和NEL vol 表现为初始下降,随后每增加1年/最后一次成像略有增加,尽管不显着(P值分别为0.382和0.46)。非进展者中的CEL ADC 和NEL ADC 并没有显示任何统计学上的显着变化,尽管有百分比呈正变化的趋势,尤其是CEL ADC 1年/最后一次影像学随访研究(P值分别为0.077和0.339)。进阶者表现出CEL ADC 和NEL ADC 的渐进负百分比变化。在进展中,与基线研究相比,NEL ADC 在第6周(P = 0.054),3个月(P = 0.023)和1年/最后(P = 0.078)下降,并且在统计学上显着在6周(P = 0.047)和3个月(P = 0.025)时与非进展者相比。对于非进步者和进步者而言,CEL ADC 和NEL ADC 随时间的变化似乎呈现出不同的趋势,其中非进步者稳定地增长到稍微进步,而进步者逐渐减少,特别是早期。这些发现表明,DWI可以用作早期治疗反应的附加成像生物标志物。扩散-ADC-阿瓦斯汀-贝伐单抗-复发性神经胶质瘤

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