Somatostatin receptors (SR) are surface markers characterizing not onl
y APUDomas associated with neuroendocrine identities but also malignan
cies without neuroendocrine expression. Recently, the somatostatin ana
log pentetreotide was labeled with In-111 (OctreoScan 111, Mallinckrod
t Medical BV, Petten, Holland) and introduced for the in vivo visualiz
ation in man of SR-positive tissues, In the present report, SR-specifi
c scintigraphy is evaluated as a clinical tool for tissue characteriza
tion in correlation with histological and radiological examinations, S
cintigraphy was focused and performed in cancer types without neuroend
ocrine tissue expression such as brain (n=6) and breast tumors (n=9) a
nd lymphomas (n=5). Scintigraphy was performed for comparison at 6 and
22 h after i.v. application of 111 MBq (3 mCi) of In-111-Pentetreotid
e. In the breast cancer group, the primary tumor was visualized in all
9 women as well as in all 4 cases,vith palpable axillary lymph nodes.
Three women with a negative axillary node scan and impalpable nodes h
ad positive biopsy, In two cases, mediastinal lymph node involvement w
as observed, So far the role of SR-positive breast cancer (BC) scans r
emains unknown. It is tempting to speculate that in resected women who
are histologically and scintigraphically SR positive, it might be of
value in the early detection of symptom-free recurrences, High densiti
es of SR were present within both meningiomas, the high-grade astrocyt
oma and the craniopharyngioma. Differentiation of low- and high-grade
astrocytomas could not be successfully achieved because both grades sh
owed intense radioactivity uptake, even though high-grade tumors lack
SR. The latter might be due to the damaged blood-brain barrier and the
poor radioactivity washout observed in high-grade astrocytomas. All f
ive lymphomas could be detected due to the presence of activated lymph
ocytes and macrophages that express SR at a sufficient density, In con
clusion, SR scintigraphy in non-neuroendocrine malignancies does not s
eem to be reliable for an initial tumor staging but rather more suitab
le for a tissue characterization and extremely useful for monitoring c
hanges of SR expression after treatment.