Treatment options for
acromegaly include surgical removal of the
adenoma,
radiotherapy, or pharmacological reduction of
growth hormone (GH) levels by
dopamine agonists or
somatostatin analogs. Whether such treatment can truly cure
acromegaly is debatable. A problem with evaluating efficacy of treatment is the lack of consensus of what constitutes a cure. Despite modern neurosurgical techniques for resecting
GH-secreting pituitary adenomas, more than 50% of patients may have persistent GH hypersecretion;
radiotherapy may take years to produce an effect. There is thus interest in pharmacological relief of symptoms and reduction in GH secretion. We report on eight patients with a biochemical diagnosis of
acromegaly (failure of suppression of GH levels to < 2.5 micrograms/L following a
glucose tolerance test [GTT]). The use of
Sandostatin-LAR (Sandoz Pharma Ltd, Basel, Switzerland) in doses of 20 to 30 mg intramuscularly at 4 week intervals produced consistent and therapeutic serum
octreotide concentrations, suppressed GH secretion to 5 micrograms/L in all eight subjects, lowered
insulin-like growth factor-1 (IGF-1) levels in all and normalized values in seven of eight, improved or led to disappearance of symptoms and signs, and was not associated with an increase in adverse events as compared with subcutaneous treatment.