Mr. Johnson et al., PHARMACOKINETICS AND EFFICACY OF THE LONG-ACTING SOMATOSTATIN ANALOG SOMATULINE IN ACROMEGALY, European journal of endocrinology, 130(3), 1994, pp. 229-234
The aim of this work was to assess the use of a sustained-release form
ulation of somatuline, a long-acting analogue of somatostatin, in the
treatment of acromegaly. Fifteen patients with active acromegaly, as d
efined by random growth hormone (GH) levels greater than 10 mU/l, whic
h fail to be suppressed to less than 5 mU/l following an oral glucose
load, were studied. Somatuline was administered as an intramuscular in
jection in two regimens: eight patients were given a single injection
of the sustained-release formulation and blood samples taken over the
next month for the measurement of both basal levels of GH and the GH r
esponse to thyrotrophin-releasing hormone; and eight patients were giv
en injections of the sustained-release formulation at 2-week intervals
over a 6-month period and basal plasma GH levels and the GH response
to both an oral glucose load and to thyrotrophin-releasing hormone was
assessed. Following a single intramuscular dose of the sustained-rele
ase preparation, random GH levels were reduced to below 10 mU/l in fiv
e patients and by greater than 50% of basal levels in the remainder. T
he insulin-like growth factor I (IGF-I) levels fell to within the norm
al range in three patients. In the long-term efficacy study, GH levels
were reduced to < 10 mU/l in 7/8 patients. The IGF-I levels were norm
alized in four patients. Five of the eight patients experienced diarrh
oea, two of mild and three of moderate severity; none of the patients
withdrew from the study. Somatuline has been shown to be effective in
the treatment of acromegaly. In its sustained-release formulation it c
learly represents a useful therapeutic advance, although at the dosage
and frequency of injection used in the current protocols it did not p
rovide optimum GH suppression in all patients.