The medical treatment of neuroendocrine GEP tumours must be based on the gr
owth properties of the tumour. Medical treatment includes chemotherapy, som
atostatin analogues and alpha interferons. Chemotherapy has been particular
ly active in patients with high proliferating neuroendocrine tumours such a
s endocrine pancreatic tumours and lung carcinoids. Streptozotocin-based co
mbinations including 5-flourouracil and doxorubicin have generated partial
remissions in 40%-60% of the patients giving a median survival of about two
years in patients with advanced disease. Cisplatinum plus etoposide have d
emonstrated significant antitumour effects in anaplastic endocrine pancreat
ic tumours and lung carcinoids. However, in low proliferating tumours such
as classical midgut carcinoids the response rates with the same combination
s of cytotoxic agents have only generated short lasting responses in less t
han 10% of patients. In these patients, biological treatment has been of be
nefit. Alpha interferon at doses of 3-9 million units three to seven times
per week subcutaneously, has given biochemical response rates of 50% and si
gnificant tumour reduction in about 15% of patients with Iona duration, up
to three years.
Somatostatin analogues have been widely used in the treatment of neuroendoc
rine gut and pancreatic tumours. The currently available somatostatin analo
gues particularly bind somatostatin receptor 2 and 5 and with low affinity
also receptor subtype 3. Octreotide is registered in most countries for the
treatment of patients with carcinoid syndrome and also VIP and glucagon pr
oducing tumours. Regular octreotide at standard doses of 100-300 mug/day gi
ves symptomatic responses in a medium of 60% of patients and biochemical re
sponses in up to 70% of patients. Significant tumour responses are rare, le
ss than 5%. Long-acting formulations of somatostatin analogues have been of
significant benefit for the patients with similar response rates as for re
gular formulations. The quality of life has been significantly improved by
using the long-acting formulations.