高级MRI在高级别胶质瘤治疗后随访中的定性评估:我们是否同意?

Nader Zakhari, Michael Taccone, Carlos Torres, Santanu Chakraborty, John Sinclair, John Woulfe, Gerard Jansen, Greg Cron, Thanh B Nguyen
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引用次数: 1

摘要

目的:MRI是高级别胶质瘤的常用随访手段。我们的目的是评估在治疗的高级别胶质瘤的情况下,越来越多地使用各种传统和先进的MR技术进行视觉定性评估,并与完善的定量测量进行比较。方法:我们前瞻性地招募了在治疗后3T MR检查(包括DWI, DCE和DSC序列)中切除新增强病灶的HGG患者。两名神经放射学家通过将ROI放置在代表性的后处理图上,客观地评估了弥散和灌注图。主观评价对比后、灌注和扩散序列。计算了判读间一致性和一致性相关系数。结果:共纳入28个病灶。定性评价的判据一致性k-trans为良好(k = 0.73), Vp为中等(k = 0.52), AUC和Ve图为一般(k = 0.37和0.21),校正CBV为一般(k = 0.39),增强模式和扩散限制存在较差(k = 0.02和0.07)。AUC和Vp (ρc = 0.98和0.97)的一致性较好,k-trans和校正CBV (ρc = 0.94)的一致性中等,Ve和ADC (ρc = 0.86和0.24)的一致性较差。结论:虽然DSC和DCE灌注图的定量测量显示令人满意的一致性,但定性评估在观察者之间的一致性较低,不应仅依赖于解释。同样,对增强模式和扩散限制解释的评分者之间的次优一致可能限制了它们在区分胶质瘤复发和治疗相关变化方面的有用性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Qualitative Assessment of Advanced MRI in Post-Treatment High Grade Gliomas Follow Up: Do We Agree?

Purpose: MRI is commonly used in follow up of high grade glioma. Our purpose is to assess the interrater agreement on the increasingly used visual qualitative assessment of various conventional and advanced MR techniques in the setting of treated high grade glioma in comparison to the well established quantitative measurements.

Methods: We prospectively enrolled HGG patients who underwent reresection of a new enhancing lesion on post-treatment 3T MR examination including DWI, DCE and DSC sequences. Two neuroradiologists objectively assessed the diffusion and perfusion maps by placing ROI on representative post-processed maps. They subjectively assessed the post-contrast, perfusion and diffusion sequences. Interrater agreement and concordance correlation coefficient were calculated.

Results: Twenty-eight lesions were included. The interrater agreement on the qualitative assessment was good for k-trans (k = 0.73), moderate for Vp (k = 0.52), fair for AUC and Ve maps (k = 0.37 and 0.21), fair for corrected CBV (k = 0.39) and poor for the enhancement pattern and presence of diffusion restriction (k = 0.02 and 0.07). The concordance between the quantitative measurements was substantial for AUC and Vp (ρc = 0.98 and 0.97), moderate for k-trans and corrected CBV (ρc = 0.94) and poor for Ve and ADC (ρc = 0.86 and 0.24).

Conclusion: While the quantitative measurements of DSC and DCE perfusion maps show satisfactory inter-rater agreement, the qualitative assessment has lower interobserver agreement and should not be relied upon solely in the interpretation. Similarly, the suboptimal inter-rater agreement on the interpretation of enhancement pattern and diffusion restriction potentially limits their usefulness in differentiating glioma recurrence from treatment related changes.

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