Ga-68 DOTATATE PET/CT成像中的正常变异、缺陷和伪影

Nico Malan, Mboyo-Di-Tamba Vangu
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引用次数: 0

摘要

三十多年来,Indium 111 DTPA Octreotide(Octreoscan)一直是核医学生长抑素受体(SSTR)成像的支柱。PET/CT的出现带来了生长抑素的新类似物,由于其标记用于正电子成像的镓68,因此具有更高的亲和力和改进的分辨率。最常用的类似物包括DOTATATE、DOTATOC和DOTANOC。然而,镓68–1,4,7,10-四氮杂环十二烷-1,4,7,10-四乙酸(DOTA)-奥曲酸(DOTATE)可能是最常见的非FDG(氟-2-脱氧葡萄糖)PET示踪剂,与PSMA(前列腺特异性膜抗原)并列。与F18标记的FDG相比,由于Ga68发生器的可用性,它不需要接近回旋加速器。DOTATATE是一种生长抑素类似物,可以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、表征和再分期。68Ga-DOTATE与18F-FDG具有互补作用,其中肿瘤可能表现出不同程度的分化。此外,它还可作为治疗的前奏,用于选择使用治疗方法进行肽受体放射性核素治疗的患者。对放射性示踪剂的正常生物分布有充分的了解,对于最佳的患者结果和避免潜在的假阳性(如炎症、正常的胰腺钩突摄取和成骨细胞活性)至关重要。在这篇综述中,我们将在图像的支持下描述68Ga-DOTATE的正常外观和潜在的陷阱,以帮助改进对这一关键创新工具的解释,从而管理表达SSTR的肿瘤个体。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Normal Variants, Pitfalls and Artifacts in Ga-68 DOTATATE PET/CT Imaging.

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.

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