Preclinical and clinical evaluation of O-[11C]methyl-L-tyrosine for tumor imaging by positron emission tomography

被引:16
|
作者
Ishiwata, K [1 ]
Tsukada, H
Kubota, K
Nariai, T
Harada, N
Kawamura, K
Kimura, Y
Oda, K
Iwata, R
Ishii, K
机构
[1] Tokyo Metropolitan Inst Gerontol, Positron Med Ctr, Itabashi Ku, Tokyo 1730022, Japan
[2] Hamamatsu Photon KK, Cent Res Lab, Hamakita 4348601, Japan
[3] Int Med Ctr Japan, Div Nucl Med, Dept Radiol, Shinjuku Ku, Tokyo 1628655, Japan
[4] Tokyo Med & Dent Univ, Dept Neurosurg, Bunkyo Ku, Tokyo 1138519, Japan
[5] SHI Accelerator Serv Ltd, Shinagawa Ku, Tokyo 1418686, Japan
[6] Tohoku Univ, CYRIC, Aoba Ku, Sendai, Miyagi 9808578, Japan
基金
日本学术振兴会;
关键词
O-[C-11]methyl-L-tyrosine; tumor imaging; positron emission tomography;
D O I
10.1016/j.nucmedbio.2004.11.005
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
We performed preclinical and clinical studies of O-[C-11]methyl-L-tyrosine, a potential tracer for imaging amino acid transport Of tumors by positron emission tomography (PET). Examinations of the radiation-absorbed dose by O-[C-11]methyl-L-tyrosine and the acute toxicity and mutagenicity of O-methyl-L-tyrosine showed suitability of the tracer for clinical use. The whole-body imaging of monkeys and healthy humans by PET showed low uptake of O-[C-11]methyl-L-tyrosine in all normal organs except for the urinary track and bladder, suggesting that the O-[C-11]methyl-L-tyrosine PET has the potential for tumor imaging in the whole-body. Finally, the brain tumor imaging was preliminarily demonstrated. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:253 / 262
页数:10
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