“…SS analogues bind with high affinity to SS receptor subtypes 2 and 5 which are found in a large variety of NETs, adenocarcinomas, inflammatory and immune cells (18,39). The most commonly-used SS analogue, octreotide, was initially conjugated with DTPA (diethylene-triamine-penta-acetic acid), but more recently to DOTA (1,4,7,10-tetraazacyclododecane-1,4,7, 10-tetra-acetic acid) as a way of coupling SS analogues with various radioisotopes, mainly 111 In (21,26,40). Scintigraphy with 111 In-octreotide is superior to 111 In-lanreotide and has a detection rate of 67 -100% for all NETs; it can therefore be used for the diagnosis, staging and follow-up of patients with NETs (9,41,42).…”