Somatostatin-receptor (SS-R) scintigraphy successfully shows primary c
ancers and distant metastases in most patients with carcinoids, islet
cells tumours, and paragangliomas. Previous in-vitro studies indicated
that somatostatin receptors are present in human breast cancers. We r
eport positive scintigraphy with [In-111-DTPA-D-Phe(1)]-octreotide in
39 of 52 primary breast cancers (75%). Parallel in-vitro autoradiograp
hy with [I-125-Tyr(3)]-octreotide of 30 of these showed a correspondin
g somatostatin-receptor status in 28. Significantly more invasive duct
al cancers could be shown than invasive lobular carcinomas (85% vs 56%
; p < 0.05). Also the number of T-1 cancers which were shown was highe
r than T-1 (86% vs 61%; p < 0.05). Imaging of the axillae showed non-p
alpable cancer-containing lymphnodes in 4 of 13 patients with subseque
ntly histologically-proven metastases. In the follow-up after a mean o
f 2.5 yr, SS-R scintigraphy in 28 of the 37 patients with an originall
y SS-R-positive cancer, was positive in the 2 patients with clinically
-recognised metastases, as well as in 6 of the remaining 26 patients w
ho were symptom-free. Raised carcinoembryonic antigent (CEA) and CA 15
-3 values were observed in only 2 and 1, respectively, of these patien
ts. Most primary breast cancers can be shown by SS-R scintigraphy, esp
ecially invasive ductal cancers. This technique may be of value in sel
ecting patients for clinical trials with somatostatin analogues or oth
er medical treatments. Furthermore, SS-R scintigraphy is more sensitiv
e than measurements of the usual serum cancer markers for detecting re
currences of SS-R-positive breast cancer.