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镓-68 DOTATATE PET/CT成像中的正常变异、陷阱与伪影

Normal Variants, Pitfalls and Artifacts in Ga-68 DOTATATE PET/CT Imaging.

作者信息

Malan Nico, Vangu Mboyo-Di-Tamba

机构信息

Division of Nuclear Medicine and Molecular Imaging, Department of Radiation Sciences, University of the Witwatersrand, Johannesburg, South Africa.

出版信息

Front Nucl Med. 2022 Feb 7;2:825486. doi: 10.3389/fnume.2022.825486. eCollection 2022.

Abstract

Indium 111 DTPA Octreotide (Octreoscan) has been the pillar of Somatostatin receptor (SSTRs) imaging in nuclear medicine for over three decades. The advent of PET/CT brought new analogs of somatostatin that have higher affinity and improved resolution due to their labeling to Gallium 68 for positron imaging. The most used analogs include DOTATATE, DOTATOC and DOTANOC. However, Gallium 68-1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid (DOTA)-octreotate (DOTATATE) is probably the most common non-FDG (fluoro-2-deoxy glucose) PET tracer alongside PSMA (prostate specific membrane antigen). In contrast to F18-labeled FDG, it does not require proximity to a cyclotron due to the availability of the Ga68 generator. DOTATATE is a somatostatin analog which allows whole body imaging of somatostatin receptors on cell surfaces. 68Ga-DOTA compounds provide the imaging standard for well-differentiated (Grade 1 and low grade 2) neuro-endocrine tumors (NETs) and is utilized in the staging and characterization and restaging of patients with NETs. 68Ga DOTATATE has a complementary role with 18F-FDG where tumors may exhibit varying degrees of differentiation. It furthermore has application as a prelude to therapy in selecting patients for peptide receptor radionuclide therapy using a theranostic approach. A sound knowledge of the normal biodistribution of the radiotracer is imperative for optimal patient outcome and to avoid potential false positives such as inflammation, normal pancreatic uncinate process uptake and osteoblastic activity. In this review, we will describe the normal appearances of the 68Ga DOTATATE and the potential pitfalls with the support of images to aid in improving interpretation of this crucial innovative tool in the management of individuals with tumors expressing SSTRs.

摘要

钆111二乙三胺五乙酸奥曲肽(奥曲肽扫描)三十多年来一直是核医学中生长抑素受体(SSTRs)成像的支柱。PET/CT的出现带来了新的生长抑素类似物,由于它们用镓68标记用于正电子成像,具有更高的亲和力和更好的分辨率。最常用的类似物包括镓68-1,4,7,10-四氮杂环十二烷-1,4,7,10-四乙酸(DOTA)-奥曲肽(DOTATATE)。与18F标记的氟代脱氧葡萄糖(FDG)不同,由于有镓68发生器,它不需要靠近回旋加速器。DOTATATE是一种生长抑素类似物,可对细胞表面的生长抑素受体进行全身成像。68Ga-DOTA化合物为高分化(1级和低2级)神经内分泌肿瘤(NETs)提供了成像标准,并用于NETs患者的分期、特征描述和再分期。68Ga DOTATATE与18F-FDG具有互补作用,因为肿瘤可能表现出不同程度的分化。此外,它还可作为使用治疗诊断方法为肽受体放射性核素治疗选择患者的治疗前奏。对于最佳的患者治疗结果以及避免潜在的假阳性,如炎症、正常胰腺钩突摄取和成骨活性,对放射性示踪剂正常生物分布的充分了解至关重要。在本综述中,我们将借助图像描述68Ga DOTATATE的正常表现以及潜在的陷阱,以帮助改进对这一关键创新工具的解读,用于管理表达SSTRs的肿瘤患者。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d0b4/11440971/9573a9621f23/fnume-02-825486-g0001.jpg

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