Long-term palliation in metastatic carcinoid tumours with various applications of meta-iodobenzylguanidin (MIBC): pharmacological MIBG, I-131-labelled MIBG and the combination
H. Zuetenhorst et al., Long-term palliation in metastatic carcinoid tumours with various applications of meta-iodobenzylguanidin (MIBC): pharmacological MIBG, I-131-labelled MIBG and the combination, EUR J GASTR, 11(10), 1999, pp. 1157-1164
Carcinoid tumours are rare, but well known for their characteristic present
ation with diarrhoea and flushes due to overproduction of serotonin in the
case of liver metastases, Treatment is mainly based on the reduction of vas
oactive peptide hypersecretion and symptomatic improvement. Octreotide and
interferon are widely applied and effective treatment options to induce sym
ptomatic improvement and, to a lesser extent, biochemical response. The mai
n drawbacks, however, are the need for frequent injections and/or the occur
rence of side effects.
A rather new approach is the application of metaiodobenzylguanidine (MIBG),
which resembles noradrenalin and serotonin, In carcinoid patients, MIBG is
taken up in the tumour cells and stored in the neurosecretory granules. Wh
en labelled with (131)iodine, radionuclide imaging is positive in up to 70%
of the patients. In these patients, two cycles of a therapeutic dose of ra
dioactive MIBG may induce long-lasting palliation (8 months) by internal ir
radiation, Also, the non-radioactive MIBG compound may be effective in pall
iation, even in patients with a negative scan. The mode of action is based
on specific tumour acidification as found in animal models, and/or based on
its effect as a false neurotransmittor.
Three case reports demonstrate different therapeutic possibilities of MIBG:
1) symptomatic relief with unlabelled MIBG, which is a safe and simple tre
atment; 2) the longterm palliation following radioactive treatment; and 3)
an additional new aspect of predosing with unlabelled MIBG followed by radi
oactive MIBG led to improved tumour targeting and impressive clinical respo
nse. fur J Gastroenterol Hepatol 11:1157-1164 (C) 1999 Lippincott Williams
& Wilkins.