Peptide and pseudo-peptide 64CU radiopharmaceuticals

被引:4
|
作者
Mirzaei, Siroos [1 ]
Lipp, Rainer W. [2 ]
机构
[1] Wilhelminenspital Stadt Wien, Dept Nucl Med, PET Ctr, Vienna, Austria
[2] Med Univ Graz, Dept Internal Med, Div Oncol, Graz, Austria
关键词
Positron emission tomography computed tomography; Copper-64; Radiopharmaceuticals; NEUROENDOCRINE TUMORS; (CUCL2)-CU-64 PET/CT; CU-64-DOTATATE; HEAD; RADIOIMMUNOTHERAPY; EXPRESSION; GUIDELINES; COPPER-64; CARCINOMA; DIAGNOSIS;
D O I
10.23736/S1824-4785.20.03311-7
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
In recent years, the introduction of theranostic twins for specific diagnosis and treatment in patients with neuroendocrine tumors became a nuclear medicine success story. Cu-64/F-18 labeled prostate specific membrane antigen (PSMA) for molecular imaging with PET-CT and peptide radioligand therapy with Lu-177 labeled PSMA inhibitors will favorably become the next theranostic twins in nuclear medicine history. Ga-68/Cu-64/F-18 PSMA PET/CT detects metastatic prostate cancer with high diagnostic sensitivity and specificity. In addition, it can be used to select patients for radioligand therapy and evaluate therapy response. Cu-64-labeled radiopharmaceuticals such as Cu-64-PSMA, and Cu-64-somatostatin analogs are promising imaging tools in the assessment of primary disease and also in the detection of disease recurrence and to evaluate therapy response. The long half-life of Cu-64 allows the distribution of the tracer to PET centers as a satellite concept, who otherwise has no access to Ga-68 generators.
引用
收藏
页码:364 / 370
页数:7
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