Al[18F]F-NOTA-Octreotide Is Comparable to [68Ga]Ga-DOTA-TATE for PET/CT Imaging of Neuroendocrine Tumours in the Latin-American Population

被引:8
作者
Haeger, Arlette [1 ]
Soza-Ried, Cristian [1 ,2 ]
Kramer, Vasko [1 ,2 ]
Hurtado de Mendoza, Ana [1 ]
Eppard, Elisabeth [1 ,3 ]
Emmanuel, Noemie [4 ]
Wettlin, Johanna [1 ]
Amaral, Horacio [1 ,2 ]
Fernandez, Rene [1 ]
机构
[1] Nucl Med & PET CT Ctr PositronMed, Santiago 7501068, Providencia, Chile
[2] Positronpharma SA, Santiago 7500921, Providencia, Chile
[3] Univ Hosp Magdeburg, Dept Nucl Med, D-39120 Magdeburg, Germany
[4] Ion Beam Applicat, B-1348 Louvain La Neuve, Belgium
关键词
neuroendocrine tumours; SSTR; Al[F-18]F-NOTA-Octreotide; PET imaging; EPIDEMIOLOGY;
D O I
10.3390/cancers15020439
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Simple Summary In the present work we investigated the clinical utility of Al[F-18]F-NOTA-Octreotide (Al[F-18]F-OC) in comparison to [Ga-68]Ga-DOTA-TATE in patients diagnosed with neuroendocrine tumours. Our aim was to verify the recently published, promising results for Al[F-18]F-NOTA-Octreotide in the Latin-American population. Al[F-18]F-NOTA-Octreotide provided excellent image quality, detected NET lesions with high sensitivity and represents a highly promising, clinical alternative to [Ga-68]Ga-DOTA-TATE. PET imaging of neuroendocrine tumours (NET) is well established for staging and therapy follow-up. The short half-life, increasing costs, and regulatory issues significantly limit the availability of approved imaging agents, such as [Ga-68]Ga-DOTA-TATE. Al[F-18]F-NOTA-Octreotide provides a similar biodistribution and tumour uptake, can be produced on a large scale and may improve access to precision imaging. Here we prospectively compared the clinical utility of [Ga-68]Ga-DOTA-TATE and Al[F-18]F-NOTA-Octreotide in the Latin-American population. Our results showed that in patients with stage IV NETs [Ga-68]Ga-DOTA-TATE presents higher physiological uptake than Al[F-18]F-NOTA-Octreotide in the liver, hypophysis, salivary glands, adrenal glands (all p < 0.001), pancreatic uncinated process, kidneys, and small intestine (all p < 0.05). Nevertheless, despite the lower background uptake of Al[F-18]F-NOTA-Octreotide, comparative analysis of tumour-to-liver (TLR) and tumour-to-spleen (TSR) showed no statistically significant difference for lesions in the liver, bone, lymph nodes, and other tissues. Only three discordant lesions in highly-metastases livers were detected by [Ga-68]Ga-DOTA-TATE but not by Al[F-18]F-NOTA-Octreotide and only one discordant lesion was detected by Al[F-18]F-NOTA-Octreotide but not by [Ga-68]Ga-DOTA-TATE. Non-inferiority analysis showed that Al[F-18]F-NOTA-Octreotide is comparable to [Ga-68]Ga-DOTA-TATE. Hence, our results demonstrate that Al[F-18]F-NOTA-Octreotide provided excellent image quality, visualized NET lesions with high sensitivity and represents a highly promising, clinical alternative to [Ga-68]Ga-DOTA-TATE.
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页数:11
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