Poeppel, Thorsten D.; Binse, Ina; Petersenn, Stephan; Lahner, Harald; Schott, Matthias; Antoch, Gerald; Brandau, Wolfgang; Bockisch, Andreas; Boy, Christian Georg Friedrich (2013). Differential uptake of (68)Ga-DOTATOC and (68)Ga-DOTATATE in PET/CT of gastroenteropancreatic neuroendocrine tumors. In: Baum, Richard P.; Rösch, Frank (eds.) Theranostics, Gallium-68, and Other Radionuclides. A Pathway to Personalized Diagnosis and Treatment. Recent Results in Cancer Research: Vol. 194 (pp. 353-371). Berlin: Springer 10.1007/978-3-642-27994-2_18
Full text not available from this repository. (Request a copy)PURPOSE
Abundant expression of somatostatin receptors (sst) is a characteristic of neuroendocrine tumors (NET). Thus, radiolabeled somatostatin analogs have emerged as important tools for both in vivo diagnosis and therapy of NET. The two compounds most often used in functional imaging with positron emission tomography (PET) are (68)Ga-DOTATATE and (68)Ga-DOTATOC. Both analogs share a quite similar sst binding profile. However, the in vitro affinity of (68)Ga-DOTATATE in binding the sst subtype 2 (sst2) is approximately tenfold higher than that of (68)Ga-DOTATOC. This difference may affect their efficiency in detection of NET lesions, as sst2 is the predominant receptor subtype on gastroenteropancreatic NET. We thus compared the diagnostic value of PET/CT with both radiolabeled somatostatin analogs ((68)Ga-DOTATATE and (68)Ga-DOTATOC) in the same patients with gastroenteropancreatic NET.
PATIENTS AND METHODS
Twenty-seven patients with metastatic gastroenteropancreatic NET underwent (68)Ga-DOTATOC and (68)Ga-DOTATATE PET/CT as part of the workup before prospective peptide receptor radionuclide therapy (PRRT). The performance of both imaging methods was analyzed and compared for detection of individual lesions per patient and for eight defined body regions. A region was regarded as positive if at least one lesion was detected in that region. In addition, radiopeptide uptake in terms of the maximal standardized uptake value (SUV(max)) was compared for concordant lesions and renal parenchyma.
RESULTS
Fifty-one regions were found positive with both (68)Ga-DOTATATE and (68)Ga-DOTATOC. Overall, however, significantly fewer lesions were detected with (68)Ga-DOTATATE in comparison with (68)Ga-DOTATOC (174 versus 179, p < 0.05). Mean (68)Ga-DOTATATE SUV(max) across all lesions was significantly lower compared with (68)Ga-DOTATOC (16.9 ± 6.8 versus 22.1 ± 12.0, p < 0.01). Mean SUV(max) for renal parenchyma was not significantly different between (68)Ga-DOTATATE and (68)Ga-DOTATOC (12.6 ± 2.6 versus 12.6 ± 2.7).
CONCLUSIONS
(68)Ga-DOTATOC and (68)Ga-DOTATATE possess similar diagnostic accuracy for detection of gastroenteropancreatic NET lesions (with a potential advantage of (68)Ga-DOTATOC) despite their evident difference in affinity for sst2. Quite unexpectedly, maximal uptake of (68)Ga-DOTATOC tended to be higher than its (68)Ga-DOTATATE counterpart. However, tumor uptake shows high inter- and intraindividual variance with unpredictable preference of one radiopeptide. Thus, our data encourage the application of different sst ligands to enable personalized imaging and therapy of gastroenteropancreatic NET with optimal targeting of tumor receptors.
Item Type: |
Book Section (Book Chapter) |
|---|---|
Division/Institute: |
04 Faculty of Medicine > Department of Radiology, Neuroradiology and Nuclear Medicine (DRNN) > Clinic of Nuclear Medicine |
UniBE Contributor: |
Boy, Christian Georg Friedrich |
Subjects: |
600 Technology > 610 Medicine & health |
ISSN: |
0080-0015 |
ISBN: |
978-3-642-27993-5 |
Series: |
Recent Results in Cancer Research |
Publisher: |
Springer |
Language: |
English |
Submitter: |
Franziska Nicoletti |
Date Deposited: |
25 Jun 2014 16:35 |
Last Modified: |
05 Dec 2022 14:32 |
Publisher DOI: |
10.1007/978-3-642-27994-2_18 |
PubMed ID: |
22918768 |
URI: |
https://boris.unibe.ch/id/eprint/47916 |
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