Objective and design: Eighteen active acromegalics entered a prospective op
en study with cabergoline (CAB), a dopaminergic drug much more potent than
bromocriptine (Br).
Methods: CAB was administered for 6 months at doses ranging between 0.5mg t
wice weekly and 0.5 mg/day. Clinical-anamnestic characteristics of the pati
ents were: (i) sensitivity to dopamine agonist drugs (10 patients): (ii) re
sistance to somatostatin analogs (SAs) (8 patients); (iii) intolerance to S
A (3 patients). In 2 patients marked hyperprolactinemia was present.
Results: Basal GH was 6.6 mu g/l (2.2=50) (median (range)), and on treatmen
t it was 3.5 mu g/l (1.2-34) (P=0.013). The corresponding IGF-I Values were
720 mu g/l (410-1438) and 375 mu g/l (167-1260) respectively (P=0.00001).
Individual GH levels decreased below 2 mu g/l in 5 patients, and between 2
and 5 mu g/l in another 5 patients. IGF-I levels were suppressed below 50%
of baseline in 8 patients and normal age-adjusted IGF-I values were reached
in 5 patients (27% of the series). The retrospective comparison with previ
ous chronic treatment with Br in the 10 suitable patients showed a greater
effectiveness of CAB (IGF-I decrease on CAB treatment, 46.8%, on Br treatme
nt, 31%, P=0.02). Adenoma shrank in the 3 patients whose pituitary imaging
was repeated during CAB.
Conclusions: These results envisage that CAB may represent a worthy therape
utic tool in acromegalic patients, inducing a degree of IGF-I and GH suppre
ssion comparable to SAs, administered by the oral route and much less expen
sive.