Molecular imaging of brain tumors with radiolabeled choline PET

被引:0
作者
Ferdinando Franco Calabria
Manlio Barbarisi
Vincenzo Gangemi
Giovanni Grillea
Giuseppe Lucio Cascini
机构
[1] National Research Council,Neuroimaging PET/MRI Research Unit, Institute of Molecular Bioimaging and Physiology
[2] Catanzaro,Department of Neurosurgery
[3] IBFM CNR,Department of Clinical and Experimental Medicine
[4] II University of Naples,Department of Neuroradiology
[5] Magna Graecia University,Department of Diagnostic Imaging, Nuclear Medicine Unit
[6] IRCCS Neuromed,undefined
[7] Magna Graecia University,undefined
来源
Neurosurgical Review | 2018年 / 41卷
关键词
PET; Choline; Brain tumors; Molecular imaging; PET/MRI; 18F-FDG;
D O I
暂无
中图分类号
学科分类号
摘要
Several positron emission tomography (PET) radiopharmaceuticals have been emerged in the last decade as feasible in the management of brain lesions, due to the low performance in this field of the 18F-fluoro-deoxyglucose (18F-FDG), for its high physiological gradient of distribution in the brain. Beyond its usefulness in prostate cancer imaging, the radiolabeled choline is becoming a promising tool in diagnosing benign and malignant lesions of the brain, due to a very low rate of distribution in normal white and grey matters. The aim of our review was to assess the real impact of the radiolabeled choline PET/CT in the management of brain benign lesions, brain tumors, and metastases. Furthermore, emphasis was given to the comparison between the radiolabeled choline and the other radiopharmaceuticals in this field. A literature review was performed. The radiolabeled choline is useful in the management of patients with suspected brain tumor relapse, especially in association with magnetic resonance imaging (MRI), with caution regarding its intrinsic characteristic of non-tumor-specific tracer. For the same reason, it is not useful in the early evaluation of brain lesions. Similar results are reported for other radiopharmaceuticals. The inclusion of the head in the whole-body scans for somatic tumors is necessary to ensure metastases in the brain or choline-avid benign lesions.
引用
收藏
页码:67 / 76
页数:9
相关论文
共 424 条
[1]  
Chen W(2006)18F-FDOPA PET imaging of brain tumors: comparison study with 18F-FDG PET and evaluation of diagnostic accuracy J Nucl Med 47 904-911
[2]  
Silverman DH(2015)Brain FDG PET and the diagnosis of dementia AJR Am J Roentgenol 204 76-85
[3]  
Delaloye S(2014)The utility of 18F-fluorodeoxyglucose PET (FDG PET) in epilepsy surgery Epilepsy Res 108 1306-1314
[4]  
Czernin J(2013)Low positive yield from routine inclusion of the brain in whole-body 18F-FDG PET/CT imaging for noncerebral malignancies: results from a large population study Nucl Med Commun 36 540-543
[5]  
Kamdar N(2008)Metabolic assessment of gliomas using 11C-methionine, [18F] fluorodeoxyglucose, and 11C-choline positron-emission tomography AJNR Am J Neuroradiol 29 1176-1182
[6]  
Pope W(2007)Uptake of 18F-Fluorocholine, 18F-FET, and 18F-FDG in C6 gliomas and correlation with 131I-SIP(L19), a marker of angiogenesis J Nucl Med 48 608-614
[7]  
Satyamurthy N(2009)Comparative evaluation of F-18 FDOPA, F-18 FDG, and F-18 FLT-PET/CT for metabolic imaging of low grade gliomas Clin Nucl Med 34 878-883
[8]  
Schiepers C(2012)Molecular imaging of brain tumors with 18F-DOPA PET and PET/CT Nucl Med Commun 33 563-570
[9]  
Cloughesy T(2014)Comparison of (11)C-methionine, (11)C-choline, and (18)F-fluorodeoxyglucose-PET for distinguishing glioma recurrence from radiation necrosis Neurol Med Chir (Tokyo) 54 280-289
[10]  
Shivamurthy VK(2010)PET with (18)F-labelled choline-based tracers for tumour imaging: a review of the literature Eur J Nucl Med Mol Imaging 37 2188-2193