Literature DB >> 9849816

Cabergoline in acromegaly: a renewed role for dopamine agonist treatment?

R Cozzi1, R Attanasio, M Barausse, D Dallabonzana, P Orlandi, N Da Re, V Branca, G Oppizzi, D Gelli.   

Abstract

OBJECTIVE AND <br> DESIGN: Eighteen active acromegalics entered a prospective open study with cabergoline (CAB), a dopaminergic drug much more potent than bromocriptine (Br). <br> METHODS: CAB was administered for 6 months at doses ranging between 0.5 mg twice weekly and 0.5 mg/day. Clinical-anamnestic characteristics of the patients were: (i) sensitivity to dopamine agonist drugs (10 patients); (ii) resistance to somatostatin analogs (SAs) (8 patients): (iii) intolerance to SA (3 patients). In 2 patients marked hyperprolactinemia was present. <br> RESULTS: Basal GH was 6.6 microg/l (2.2-50) (median (range)), and on treatment it was 3.5 microg/l (1.2-34) (P=0.013). The corresponding IGF-I values were 720 microg/l (410-1438) and 375 microg/l (167-1260) respectively (P=0.00001). Individual GH levels decreased below 2 microg/l in 5 patients, and between 2 and 5 microg/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 previous 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 treatment, 31%, P=0.02). Adenoma shrank in the 3 patients whose pituitary imaging was repeated during CAB. <br> CONCLUSIONS: These results envisage that CAB may represent a worthy therapeutic tool in acromegalic patients, inducing a degree of IGF-I and GH suppression comparable to SAs, administered by the oral route and much less expensive.

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Year:  1998        PMID: 9849816     DOI: 10.1530/eje.0.1390516

Source DB:  PubMed          Journal:  Eur J Endocrinol        ISSN: 0804-4643            Impact factor:   6.664


  24 in total

1.  Cabergoline treatment in acromegaly: cons.

Authors:  Leandro Kasuki; Leonardo Vieira Neto; Mônica R Gadelha
Journal:  Endocrine       Date:  2014-02-07       Impact factor: 3.633

Review 2.  Medical management of growth hormone-secreting pituitary adenomas.

Authors:  Michael S Racine; Ariel L Barkan
Journal:  Pituitary       Date:  2002       Impact factor: 4.107

Review 3.  Medical therapy in acromegaly.

Authors:  Mark Sherlock; Conor Woods; Michael C Sheppard
Journal:  Nat Rev Endocrinol       Date:  2011-03-29       Impact factor: 43.330

4.  Pegvisomant and cabergoline combination therapy in acromegaly.

Authors:  I Bernabeu; C Alvarez-Escolá; A E Paniagua; T Lucas; I Pavón; J M Cabezas-Agrícola; F F Casanueva; M Marazuela
Journal:  Pituitary       Date:  2013-03       Impact factor: 4.107

5.  Cabergoline decreases somatotroph adenoma size: a case report.

Authors:  Michael R Rickels; Peter J Snyder
Journal:  Pituitary       Date:  2004       Impact factor: 4.107

Review 6.  Clinical pharmacokinetics of cabergoline.

Authors:  Paolo Del Dotto; Ubaldo Bonuccelli
Journal:  Clin Pharmacokinet       Date:  2003       Impact factor: 6.447

7.  Prolactinomas, Cushing's disease and acromegaly: debating the role of medical therapy for secretory pituitary adenomas.

Authors:  Beverly Mk Biller; Annamaria Colao; Stephan Petersenn; Vivien S Bonert; Marco Boscaro
Journal:  BMC Endocr Disord       Date:  2010-05-17       Impact factor: 2.763

Review 8.  Somatostatin analogs in medical treatment of acromegaly.

Authors:  Michael S Racine; Ariel L Barkan
Journal:  Endocrine       Date:  2003-04       Impact factor: 3.633

Review 9.  Medical therapy: options and uses.

Authors:  John D Carmichael; Vivien S Bonert
Journal:  Rev Endocr Metab Disord       Date:  2008-03       Impact factor: 6.514

Review 10.  Medical therapy of pituitary adenomas: effects on tumor shrinkage.

Authors:  Annamaria Colao; Rosario Pivonello; Carolina Di Somma; Silvia Savastano; Ludovica F S Grasso; Gaetano Lombardi
Journal:  Rev Endocr Metab Disord       Date:  2009-06       Impact factor: 6.514

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