Treatment of
acromegaly is effective in reversing the reduced life-span of patients only when serum
growth hormone (GH) concentrations are lowered to less than 2.5 micrograms/l. Usual treatments achieve this goal in no more than 50-60% of patients. The effects of
octreotide were studied in a prospective, open label study with 68 acromegalic patients enrolled in 10 Italian centers.
Octreotide was administered sc at a dose of 100 micrograms t.i.d. for 1 year. After 3 months of
therapy,
octreotide was effective in decreasing serum GH levels below 2.5 micrograms/l in 16 out of 64 acromegalic patients (25%). Fifteen of them had pretreatment GH levels below 25 micrograms/l.
Insulin-like growth factor I (
IGF-I) levels normalized in about 40% of patients. No further GH reduction was observed after 1 year of treatment. The presence of abnormal GH responses to
thyrotropin-releasing hormone (TRH) and
gonadotropin-releasing hormone was reduced from 54 to 24% and from 16 to 12%, respectively.
Tumor shrinkage was observed in 50% of 26 non-irradiated patients after 12 months of treatment. Both basal and TRH-stimulated serum
prolactin levels significantly decreased in the 11 hyperprolactinemic patients. Although serum
thyrotropin, free
triiodothyronine and free
thyroxine concentrations were not modified, a significant reduction of
thyrotropin response to TRH was observed in the 9th month of
therapy. In non-diabetic patients, an increase of mean
blood glucose levels without modifications of fasting morning concentrations was found. About one-quarter of the patients with overt
diabetes mellitus had an impairment of their metabolic control. Main clinical symptoms of
acromegaly improved in 70-80% of patients.(ABSTRACT TRUNCATED AT 250 WORDS)