Colocalization of Gadolinium-Diethylene Triamine Pentaacetic Acid With High-Molecular-Weight Molecules After Intracerebral Convection-Enhanced Delivery in Humans

被引:61
作者
Sampson, John H. [1 ,2 ]
Brady, Martin [3 ]
Raghavan, Raghu [3 ]
Mehta, Ankit I. [1 ]
Friedman, Allan H. [1 ]
Reardon, David A. [1 ,4 ]
Petry, Neil A. [5 ]
Barboriak, Daniel P. [5 ]
Wong, Terence Z. [5 ]
Zalutsky, Michael R. [5 ]
Lally-Goss, Denise [1 ]
Bigner, Darell D. [2 ]
机构
[1] Duke Univ, Med Ctr, Div Neurosurg, Dept Surg, Durham, NC 27710 USA
[2] Duke Univ, Med Ctr, Dept Pathol, Durham, NC 27710 USA
[3] Therataxis LLC, Baltimore, MD USA
[4] Duke Univ, Med Ctr, Dept Pediat, Durham, NC 27710 USA
[5] Duke Univ, Med Ctr, Dept Radiol, Durham, NC 27710 USA
基金
美国国家卫生研究院;
关键词
Brain neoplasms; Convection; Drug delivery systems; Gadolinium DTPA; Iodine radioisotopes; Magnetic resonance imaging; Positron-emission tomography; GLIOBLASTOMA-MULTIFORME; TARGETED TOXIN; REAL-TIME; IN-VIVO; BRAIN; INFUSION; MICROINFUSION; GLUCOCEREBROSIDASE; EFFICACY; CHELATE;
D O I
10.1227/NEU.0b013e3182181ba8
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
BACKGROUND: Convection-enhanced delivery (CED) permits site-specific therapeutic drug delivery within interstitial spaces at increased dosages through circumvention of the blood-brain barrier. CED is currently limited by suboptimal methodologies for monitoring the delivery of therapeutic agents that would permit technical optimization and enhanced therapeutic efficacy. OBJECTIVE: To determine whether a readily available small-molecule MRI contrast agent, gadolinium-diethylene triamine pentaacetic acid (Gd-DTPA), could effectively track the distribution of larger therapeutic agents. METHODS: Gd-DTPA was coinfused with the larger molecular tracer, I-124-labeled human serum albumin (I-124-HSA), during CED of an EGFRvIII-specific immunotoxin as part of treatment for a patient with glioblastoma. RESULTS: Infusion of both tracers was safe in this patient. Analysis of both Gd-DTPA and I-124-HSA during and after infusion revealed a high degree of anatomical and volumetric overlap. CONCLUSION: Gd-DTPA may be able to accurately demonstrate the anatomic and volumetric distribution of large molecules used for antitumor therapy with high resolution and in combination with fluid-attenuated inversion recovery (FLAIR) imaging, and provide additional information about leaks into cerebrospinal fluid spaces and resection cavities. Similar studies should be performed in additional patients to validate our findings and help refine the methodologies we used.
引用
收藏
页码:668 / 676
页数:9
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