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Prospective Within-Patient Assessment of the Impact of an Unlabeled Octreotide Pre-dose on the Biodistribution and Tumor Uptake of 68 Ga DOTATOC as Assessed by Dynamic Whole-body PET in Patients with Neuroendocrine Tumors: Implications for Diagnosis and Therapy.
- Source :
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Molecular imaging and biology [Mol Imaging Biol] 2021 Oct; Vol. 23 (5), pp. 766-774. Date of Electronic Publication: 2021 Apr 07. - Publication Year :
- 2021
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Abstract
- Purpose: Gastroenteropancreatic neuroendocrine tumors (GEP NETs) are often associated with high expression of somatostatin receptors (SSTRs) which allows for PET/CT imaging with radiolabeled somatostatin analogs such as <superscript>68</superscript> Ga-DOTATOC. The interplay between <superscript>68</superscript> Ga-DOTATOC and the synthetic somatostatin analogs commonly used to manage patient symptoms may lead to competition between the labelled and unlabeled peptides for receptor binding sites and current product labelling recommends patients be taken off somatostatin analogs before imaging. In this study, we prospectively investigated in human patients the effect of a pre-dose of octreotide, a short-acting somatostatin analog, on the distribution of <superscript>68</superscript> Ga-DOTATOC in GEP NETs and normal organs.<br />Procedure: Research participants with GEP NETs were studied on two occasions using dynamic whole-body <superscript>68</superscript> Ga-DOTATOC PET/CT. The two imaging studies were performed within 21 days of each other, using an identical acquisition protocol except for the administration of 50 μg of short-acting octreotide (pre-dose) immediately before the second PET/CT. Paired t-tests were used to compare tracer uptake with and without octreotide, for tumor and various normal organs.<br />Results: Seven participants with a mean age of 53 ± 10 years were studied. Octreotide pre-dosing decreased radiotracer uptake in the normal liver and spleen by 25 % (p = 0.04) and 47 % (p = 0.05) respectively but did not significantly change uptake in tumor (p = 0.53), red marrow (p = 0.12), kidneys (p =0.57), or pituitary gland (p = 0.27).<br />Conclusions: Our data indicate SSTR imaging can be improved with a pre-dose of unlabeled octreotide given just prior to injection of the radiotracer. These data suggest there may be no need to discontinue somatostatin analog therapy prior to PET/CT with <superscript>68</superscript> Ga-DOTATOC, allowing for a simpler, less disruptive patient protocol. This approach warrants further study in a variety of settings.<br /> (© 2021. World Molecular Imaging Society.)
- Subjects :
- Adult
Female
Humans
Male
Middle Aged
Octreotide administration & dosage
Octreotide pharmacokinetics
Prospective Studies
Radiopharmaceuticals administration & dosage
Radiopharmaceuticals pharmacokinetics
Somatostatin analogs & derivatives
Tissue Distribution
Whole Body Imaging
Gallium Radioisotopes administration & dosage
Gallium Radioisotopes pharmacokinetics
Neuroendocrine Tumors diagnostic imaging
Neuroendocrine Tumors metabolism
Octreotide analogs & derivatives
Positron Emission Tomography Computed Tomography
Subjects
Details
- Language :
- English
- ISSN :
- 1860-2002
- Volume :
- 23
- Issue :
- 5
- Database :
- MEDLINE
- Journal :
- Molecular imaging and biology
- Publication Type :
- Academic Journal
- Accession number :
- 33829361
- Full Text :
- https://doi.org/10.1007/s11307-021-01600-5