ACTA FAC MED NAISS 2023;40(3):259-269 |
Review article
UDC:
616.43-006.6-073-085.84
DOI:
10.5937/afmnai40-40887
Running title: Theranostics in Neuroendocrine Tumors
Theranostics and Precision Medicine in
Neuroendocrine Tumors
Filip Veličković1,2, Marina Vlajković1,2, Miloš Stević1,2, Nina Topić1, Tamara Anđelković1,2, Đuro Macut3
1University Clinical Center Niš, Center
of Nuclear Medicine, Niš, Serbia
SUMMARY
Introduction. Neuroendocrine tumors (NETs) have increased expression
of somatostatin receptors (SSTR), where subtype 2 and 5 are the most
common. Overexpression of the SSTR is an outstanding molecular
target for inoperable and metastatic NETs that enables a unique
approach of targeted diagnosis and treatment. In addition to SSTRs,
neuroendocrine tumors also express other receptors that can be
suitable targets for visualization by nuclear medicine methods.
Aim. This review paper is focused on the most common
radiopharmaceuticals and their molecular targets that are used today
based on theranostic approach in NETs.
Results. In conventional nuclear medicine, the most important
diagnostic radiopharmaceuticals are somatostatin analogs (SSA)
labeled with 111In and 99mTc, however 99mTc
has advantages over 111In based on better physical
characteristics and better performance. In recent years, highly
potent theranostic pairs have been created for the imaging and
treatment of NETs, which can strongly bind SSTR. Derivatives of
68Ga-labeled octreotide are recommended for diagnostics and
follow-up of NENs. The great advantage of 68Ga
radiopharmaceuticals is that identical compounds can be labeled with
therapeutic radionuclides 90Y and 177Lu.
Conclusion. Peptide receptor radionuclide therapy is a systemic
molecular target therapy that has proven to be safe and very
effective in controlling the disease and prolonging the survival of
patients with advanced and inoperable NETs. With a negligible number
of adverse events, this therapy is safe and should be administered
to all patients who meet the necessary criterias, primarily
overexpression of the somatostatin receptor type 2.
Keywords: neuroendocrine tumours,
somatostatin receptor, scintigraphy, radionuclide therapy
Corresponding author:
Filip Veličković
e-mail: velickovicfilip@yahoo.com