Comparison of Dynamic Contrast-Enhancement Parameters between Gadobutrol and Gadoterate Meglumine in Posttreatment Glioma: A Prospective Intraindividual Study

被引:4
|
作者
Park, J. E. [1 ,2 ]
Kim, J. Y. [3 ]
Kim, H. S. [1 ,2 ]
Shim, W. H. [1 ,2 ]
机构
[1] Univ Ulsan, Coll Med, Asan Med Ctr, Dept Radiol, 88 Olymp Ro 43 Gil, Seoul 05505, South Korea
[2] Univ Ulsan, Coll Med, Res Inst Radiol, Asan Med Ctr, 88 Olymp Ro 43 Gil, Seoul 05505, South Korea
[3] Sungkyunkwan Univ, Sch Med, Kangbuk Samsung Hosp, Dept Radiol, Seoul, South Korea
基金
新加坡国家研究基金会;
关键词
CENTRAL-NERVOUS-SYSTEM; RECURRENT GLIOBLASTOMA; AGENTS GADOBUTROL; BRAIN-TUMORS; MRI; DIFFERENTIATION; PSEUDOPROGRESSION; PERMEABILITY; CROSSOVER; MODEL;
D O I
10.3174/ajnr.A6792
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
BACKGROUND AND PURPOSE: Differences in molecular properties between one-molar and half-molar gadolinium-based contrast agents are thought to affect parameters obtained from dynamic contrast-enhanced imaging. The aim of our study was to investigate differences in dynamic contrast-enhanced parameters between one-molar nonionic gadobutrol and half-molar ionic gadoterate meglumine in patients with posttreatment glioma. MATERIALS AND METHODS: This prospective study enrolled 32 patients who underwent 2 20-minute dynamic contrast-enhanced examinations, one with gadobutrol and one with gadoterate meglumine. The model-free parameter of area under the signal intensity curve from 30 to 1100seconds and the Tofts model-based pharmacokinetic parameters were calculated and compared intraindividually using paired t tests. Patients were further divided into progression (n=12) and stable (n=20) groups, which were compared using Student t tests. RESULTS: Gadobutrol and gadoterate meglumine did not show any significant differences in the area under the signal intensity curve or pharmacokinetic parameters of K-trans, V-e, V-p, or K-ep (all P>.05). Gadobutrol showed a significantly higher mean wash-in rate (0.83 0.64 versus 0.29 +/- 0.63, P=.013) and a significantly lower mean washout rate (0.001 +/- 0.0001 versus 0.002 +/- 0.002, P=.02) than gadoterate meglumine. Trends toward higher area under the curve, K-trans, V-e, V-p, wash-in, and washout rates and lower K-ep were observed in the progression group in comparison with the treatment-related-change group, regardless of the contrast agent used. CONCLUSIONS: Model-free and pharmacokinetic parameters did not show any significant differences between the 2 gadolinium-based contrast agents, except for a higher wash-in rate with gadobutrol and a higher washout rate with gadoterate meglumine, supporting the interchangeable use of gadolinium-based contrast agents for dynamic contrast-enhanced imaging in patients with posttreatment glioma.
引用
收藏
页码:2041 / 2048
页数:8
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