Compared with other imaging modalities and clinical investigation, the
In-111-pentetreotide scan identified additional metastatic disease si
tes in 12 carcinoid patients and 2 occult primaries, and influenced th
e therapeutic outcome in 36 patients [29 carcinoids. 2 atypical carcin
oids, 3 cancers of unknown primaries (CUPs) and 2 medullary thyroid ca
rcinomas (MCTs)]. No adverse ed reactions were noted. Somatostatin rec
eptors were detected in 59/60 carcinoid patients, 314 atypical carcino
id patients, 0/2 MCT patients, and 0/3 cases of CUP. Somatostatin rece
ptor presence is underestimated in some patients using standard hormon
al response criteria rather than scintigraphy. 18 patients with metast
atic carcinoids who underwent In-111-pentetreotide scanning were all s
omatostatin receptor positive. Their mean (+/- SE) 5-hydroxyindoleacet
ic acid (5-HIAA) suppression with octreotide therapy was -53% (+/- 6%)
, 8 patients had <50% and 10 had >50% 5-HIAA suppression (ranges: -4 t
o -47% and -58 to -94%, respectively). To investigate the effect of so
matostatin analogues on survival, 90 consecutive cases of carcinoid sy
ndrome patients treated during the somatostatin analogue era were revi
ewed. Survival according to primary site was 12.01, 18.29 and 6.05 yea
rs (overall median 12.01 years) for patients with foregut, midgut and
unknown primaries, respectively. The difference from historical contro
ls is substantial (67 vs. 18% 5-year survival), although our series is
neither prospective nor randomised. The heterogeneity in patient and
tumour response to somatostatin analogue therapy is discussed.