R. Abs et al., CABERGOLINE IN THE TREATMENT OF ACROMEGALY - A STUDY IN 64 PATIENTS, The Journal of clinical endocrinology and metabolism, 83(2), 1998, pp. 374-378
Cabergoline is a new, long acting, dopamine agonist that is more effec
tive and better tolerated than bromocriptine in patients with hyperpro
lactinemia. Because dopamine agonists still have a place in the medica
l management of acromegaly, cabergoline might be a useful treatment. W
e, therefore, evaluated the effect of long term administration of cabe
rgoline in a large group of unselected acromegalic patients. Sixty-fou
r patients were included in a multicenter, prospective, open labeled s
tudy. A subgroup of 16 patients had GH-/PRL-cosecreting pituitary aden
omas. Cabergoline was started at a dose of 1.0 mg/week and was gradual
ly increased until normalization of plasma insulinlike growth factor I
(IGF-I) levels, occurrence of unacceptable side-effects, or a maximal
weekly dose of 3.5 mg (7.0 mg in 1 case) was reached. Treatment with
cabergoline suppressed plasma IGF-I below 300 mu g/L in 39% of cases a
nd between 300-450 mu g/L in another 28%. With pretreatment plasma IGF
-I concentrations less than 750 mu g/L, a suppression of IGF-I below 3
00 mu g/L was obtained in 53% of cases, and a suppression between 300-
450 mu g/L was obtained in another 32%. By contrast, with pretreatment
plasma IGF-I concentrations above 750 mu g/L, only 17% of cases showe
d a suppression of IGF-I below 300 mu g/L, and there was IGF-I suppres
sion between 300-450 mu g/L in another 21%. In GH-/PRL-cosecreting ade
nomas, 50% of cases suppressed plasma IGF-I levels below 300 mu g/L, a
nd another 31% did so between 300-450 mu g/L, in contrast to only 35%
and 27%, respectively, in GH-secreting adenomas. Similar results were
obtained concerning the secretion of GH. Tumor shrinkage was demonstra
ted in 13 of 21 patients, with a mass reduction by more than half in 5
GH-/PRL-cosecreting adenomas. Except for slight gastrointestinal disc
omfort and orthostatic hypotension in a few patients at the beginning
of therapy, cabergoline treatment was well tolerated. Only 2 patients
stopped medication because of nausea. The weekly dose of cabergoline r
anged between 1.0-1.75 mg. A further increase in the dose was only eff
ective in 1 GH-/PRL-cosecreting adenoma. The results of this study sug
gest that cabergoline is an effective, well tolerated therapy that sho
uld be considered in the management of acromegaly, especially if the p
ituitary adenoma cosecretes GH and PRL or if pretreatment plasma IGF-I
levels are below 750 mu g/L.