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Erschienen in: European Journal of Nuclear Medicine and Molecular Imaging 1/2008

01.01.2008 | Original article

68Ga-DOTANOC: biodistribution and dosimetry in patients affected by neuroendocrine tumors

verfasst von: C. Pettinato, A. Sarnelli, M. Di Donna, S. Civollani, C. Nanni, G. Montini, D. Di Pierro, M. Ferrari, M. Marengo, C. Bergamini

Erschienen in: European Journal of Nuclear Medicine and Molecular Imaging | Ausgabe 1/2008

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Abstract

Objectives

The aim of this work was the evaluation of biodistribution and radiation dosimetry of 68Ga-DOTANOC in patients affected by neuroendocrine tumors.

Materials and methods

We enrolled nine patients (six male and three female) affected by different types of neuroendocrine tumors (NETs). Each patient underwent four whole body positron emission tomography (PET) scans, respectively, at 5, 20, 60, and 120 min after the intravenous injection of about 185 MBq of 68Ga-DOTANOC. Blood and urine samples were taken at different time points post injection: respectively, at about 5, 18, 40, 60, and 120 min for blood and every 40–50 min from injection time up to 4 h for urine. The organs involved in the dosimetric evaluations were liver, heart, spleen, kidneys, lungs, pituitary gland, and urinary bladder. Dosimetric evaluations were done using the OLINDA/EXM 1.0 software.

Results

A physiological uptake of 68Ga-DOTANOC was seen in all patients in the pituitary gland, the spleen, the liver, and the urinary tract (kidneys and urinary bladder). Organs with the highest absorbed doses were kidneys \( \left( {{{9.0{\text{E}} - 02 \pm 3.2{\text{E}} - 02{\text{mSv}}} \mathord{\left/ {\vphantom {{9.0{\text{E}} - 02 \pm 3.2{\text{E}} - 02{\text{mSv}}} {{\text{MBq}}}}} \right. \kern-\nulldelimiterspace} {{\text{MBq}}}}} \right) \). The mean effective dose equivalent (EDE) was \( {{2.5{\text{E}} - 02 \pm 4.6{\text{E}} - 03{\text{mSv}}} \mathord{\left/ {\vphantom {{2.5{\text{E}} - 02 \pm 4.6{\text{E}} - 03{\text{mSv}}} {{\text{MBq}}}}} \right. \kern-\nulldelimiterspace} {{\text{MBq}}}} \).

Discussion and conclusions

The excretion of the compound was principally via urine, giving dose to the kidney and the urinary bladder wall. As SSTR2 is the most frequently expressed somatostatin receptor and 68Ga-DOTANOC has high affinity to it, this compound might play an important role in PET oncology in the future. The dosimetric evaluation carried out by our team demonstrated that 68Ga-DOTANOC delivers a dose to organs comparable to, and even lower than, analogous diagnostic compounds.
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Metadaten
Titel
68Ga-DOTANOC: biodistribution and dosimetry in patients affected by neuroendocrine tumors
verfasst von
C. Pettinato
A. Sarnelli
M. Di Donna
S. Civollani
C. Nanni
G. Montini
D. Di Pierro
M. Ferrari
M. Marengo
C. Bergamini
Publikationsdatum
01.01.2008
Verlag
Springer-Verlag
Erschienen in
European Journal of Nuclear Medicine and Molecular Imaging / Ausgabe 1/2008
Print ISSN: 1619-7070
Elektronische ISSN: 1619-7089
DOI
https://doi.org/10.1007/s00259-007-0587-y

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