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Dynamic measurements of T1 shortening (dynamic contrast enhanced—DCE) as well as of T2<sup style="margin-left:-6px;">&#42;shortening (dynamic susceptibility contrast—DSC) as two separate measurement strategies are widely used to quantitatively describe tumor perfusion and vascularity. Dual-echo approaches allow for the simultaneous assessment of both effects. The extension to multi-echo sequences should inhere the advantage of improved signal-to-noise ratios and more precise sampling of the T2<sup style="margin-left:-6px;">&#42;decay. The aim of our study is to investigate, if an extension of the dual-echo approach to the multi-echo approach allows for more stable quantitative determination of pharmacokinetic parameters in brain tumors. This study applies a multi-echo approach to obtain different estimations of a vascular input function and analyzes various combinations of vascular input functions and pharmacokinetic models. Perfusion measurements were performed with 52 consecutive patients with different brain tumors using a 10-echo gradient echo sequence. Our findings show that the extension to multi-echo sequences leads to an 11%-improvement of the Contrast-to-Noise ratio. Compared to other combinations, an application of Extended Tofts model using the T2<sup style="margin-left:-6px;">&#42;-related venous output function or an output function estimated in the tumor tissue enables the most reliable determination of perfusion parameters, reducing the reproducibility range by a factor of 1.2 to 10 for Ktrans and of 1.2 to 5.5 in the case of rBV calculation. Determination of Ktrans within repeated measurements within about 3 days results as most stable, if AIF from tumor pixels is used as vascular input function, meaning that the scatter is reduced by a factor of 1.2 compared to the next best VIF and by a factor of 10 compared to the worst of the tested approaches. In addition, this study shows that signal decomposition into two components with different Larmor frequencies might provide additional information
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篇名 Magnetic Resonance Perfusion in Brain Tumors: Comparison of Different Evaluation Approaches in Dual-Echo and Multi-Echo Techniques
来源期刊 医学物理学、临床工程、放射肿瘤学(英文) 学科 医学
关键词 MRI BRAIN TUMORS PERFUSION
年,卷(期) 2017,(2) 所属期刊栏目
研究方向 页码范围 174-192
页数 19页 分类号 R73
字数 语种
DOI
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研究主题发展历程
节点文献
MRI
BRAIN
TUMORS
PERFUSION
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研究去脉
引文网络交叉学科
相关学者/机构
期刊影响力
医学物理学、临床工程、放射肿瘤学(英文)
季刊
2168-5436
武汉市江夏区汤逊湖北路38号光谷总部空间
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236
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0
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