Literature DB >> 11081189

Efficacy of combined treatment with lanreotide and cabergoline in selected therapy-resistant acromegalic patients.

P Marzullo1, D Ferone, C Di Somma, R Pivonello, M Filippella, G Lombardi, A Colao.   

Abstract

The aim of this study was to evaluate the efficacy of a 6-month treatment with lanreotide (LAN) (60-90 mg/month) alone and combined with cabergoline (CAB) (1.5-3 mg/week) in 10 acromegalic patients previously demonstrated to be poor responders to octreotide (OCT) (0.6 mg/day) alone and combined with quinagolide (CV) (0.6 mg/day). All patients had previously undergone unsuccessful surgery and none of them received radiotherapy. Immunohistochemistry showed intense positive GH staining in all adenomas, positive PRL staining in 5 adenomas and faint ACTH or FSH/LH positive staining in other 2 adenomas. Moderately elevated serum PRL levels (35 and 47 ng/ml) were recorded in two patients. Fasting plasma IGF-I and serum GH levels were assayed at baseline and 30, 60, 90 and 120 days after each treatment. Gallbladder ultrasonography and sellar MRI were performed before and after 6 months of OCT and LAN treatments. After OCT treatment circulating GH and IGF-I levels remained elevated in all patients, while after 3 months of combined OCT + CV treatment, serum GH levels were suppressed (below 2.5 ng/ml) in only 1 patient. Significant increase of the percent GH (83.9 +/- 4.3 vs. 70.3 +/- 5.6%, p < 0.01) and IGF-I suppression (54 +/- 4.4 vs. 45.3 +/- 5.7, p < 0.01) and decrease of the nadir of GH (8.5 +/- 1.2 vs. 14.6 +/- 1.9 ng/ml, p < 0.01) and IGF-I (400.9 +/- 32.8 vs. 462.1 +/- 45.1 ng/ml) were obtained with the combined treatment when compared to OCT treatment alone. After a 15-30 days wash-out, circulating GH and IGF-I levels significantly increased up to pretreatment level in all patients. After 6 months of treatment with LAN, suppression of serum GH was achieved in 1 patient, but no difference in GH (66.3 +/- 6.3%) and IGF-I (43.9 +/- 4.6%) suppression was recorded in comparison to OCT treatment. After 3 months of treatment with LAN combined with CAB, suppression of serum GH and normalization of plasma IGF-I levels was achieved in 4 and 5 patients, respectively. Percent suppression of GH (88.1 +/- 2.1%) and IGF-I (57.5 +/- 2.8%) was significantly greater with the combined treatment than with LAN treatment alone. In the 7 patients with evident residual mass no change was documented by magnetic resonance imaging (MRI). None of the patients withdrew LAN + CAB treatment for poor tolerance, one patient had mild hypotension. Sludge was shown after 6 months of LAN treatment in one patient without notable change after 3 months of LAN + CAB treatment. In conclusion, the treatment with dopaminergic drugs such as CV and CAB, significantly increased the efficacy of somatostatin analogs, and can be used in combined therapy in poorly responsive patients.

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Year:  1999        PMID: 11081189     DOI: 10.1023/a:1009932521242

Source DB:  PubMed          Journal:  Pituitary        ISSN: 1386-341X            Impact factor:   4.107


  29 in total

Review 1.  Clinical review 22: Therapeutic options in acromegaly.

Authors:  L A Frohman
Journal:  J Clin Endocrinol Metab       Date:  1991-06       Impact factor: 5.958

Review 2.  Acromegaly.

Authors:  S Melmed
Journal:  N Engl J Med       Date:  1990-04-05       Impact factor: 91.245

Review 3.  Octreotide.

Authors:  S W Lamberts; A J van der Lely; W W de Herder; L J Hofland
Journal:  N Engl J Med       Date:  1996-01-25       Impact factor: 91.245

4.  Prolactinomas resistant to standard dopamine agonists respond to chronic cabergoline treatment.

Authors:  A Colao; A Di Sarno; F Sarnacchiaro; D Ferone; G Di Renzo; B Merola; L Annunziato; G Lombardi
Journal:  J Clin Endocrinol Metab       Date:  1997-03       Impact factor: 5.958

5.  CV 205-502 in acromegaly.

Authors:  P G Chiodini; R Attanasio; R Cozzi; D Dallabonzana; G Oppizzi; P Orlandi; S Strada; A Liuzzi
Journal:  Acta Endocrinol (Copenh)       Date:  1993-05

6.  Dopamine agonists and pituitary tumor shrinkage.

Authors:  J S Bevan; J Webster; C W Burke; M F Scanlon
Journal:  Endocr Rev       Date:  1992-05       Impact factor: 19.871

7.  A comparison of cabergoline and bromocriptine in the treatment of hyperprolactinemic amenorrhea. Cabergoline Comparative Study Group.

Authors:  J Webster; G Piscitelli; A Polli; C I Ferrari; I Ismail; M F Scanlon
Journal:  N Engl J Med       Date:  1994-10-06       Impact factor: 91.245

8.  Long-term treatment of acromegaly with the slow-release somatostatin analogue lanreotide.

Authors:  J Marek; V Hána; M Krsek; V Justová; F Catus; F Thomas
Journal:  Eur J Endocrinol       Date:  1994-07       Impact factor: 6.664

9.  The role of prolactin in the inhibitory action of bromocriptine on growth hormone secretion in acromegaly.

Authors:  S W Lamberts; J G Klijn; C C van Vroonhoven; S Z Stefanko; A Liuzzi
Journal:  Acta Endocrinol (Copenh)       Date:  1983-08

10.  CV 205-502 treatment in therapy-resistant acromegalic patients.

Authors:  G Lombardi; A Colao; D Ferone; F Sarnacchiaro; P Marzullo; A Di Sarno; E Rossi; B Merola
Journal:  Eur J Endocrinol       Date:  1995-05       Impact factor: 6.664

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  18 in total

Review 1.  International Union of Basic and Clinical Pharmacology. CV. Somatostatin Receptors: Structure, Function, Ligands, and New Nomenclature.

Authors:  Thomas Günther; Giovanni Tulipano; Pascal Dournaud; Corinne Bousquet; Zsolt Csaba; Hans-Jürgen Kreienkamp; Amelie Lupp; Márta Korbonits; Justo P Castaño; Hans-Jürgen Wester; Michael Culler; Shlomo Melmed; Stefan Schulz
Journal:  Pharmacol Rev       Date:  2018-10       Impact factor: 25.468

2.  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 3.  Update on the medical management of pituitary adenomas.

Authors:  Cheryl A Pickett
Journal:  Curr Neurol Neurosci Rep       Date:  2005-05       Impact factor: 5.081

Review 4.  The role of combination medical therapy in the treatment of acromegaly.

Authors:  Dawn Shao Ting Lim; Maria Fleseriu
Journal:  Pituitary       Date:  2017-02       Impact factor: 4.107

5.  Insulin-like growth factor-1 is essential to the increased mortality caused by excess growth hormone: a case of thyroid cancer and non-Hodgkin's lymphoma in a patient with pituitary acromegaly.

Authors:  A Taslipinar; E Bolu; L Kebapcilar; M Sahin; G Uckaya; M Kutlu
Journal:  Med Oncol       Date:  2008-07-29       Impact factor: 3.064

Review 6.  Guidelines for the treatment of growth hormone excess and growth hormone deficiency in adults.

Authors:  A Giustina; A Barkan; P Chanson; A Grossman; A Hoffman; E Ghigo; F Casanueva; A Colao; S Lamberts; M Sheppard; S Melmed
Journal:  J Endocrinol Invest       Date:  2008-09       Impact factor: 4.256

Review 7.  Comparison of efficacy and tolerability of somatostatin analogs and other therapies for acromegaly.

Authors:  Morton G Burt; Ken K Y Ho
Journal:  Endocrine       Date:  2003-04       Impact factor: 3.633

Review 8.  Somatostatin analogs in treatment of non-growth hormone-secreting pituitary adenomas.

Authors:  Annamaria Colao; Mariagiovanna Filippella; Carolina Di Somma; Simona Manzi; Francesca Rota; Rosario Pivonello; Maria Gaccione; Michele De Rosa; Gaetano Lombardi
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.  Modern treatment of acromegaly.

Authors:  Z Merza
Journal:  Postgrad Med J       Date:  2003-04       Impact factor: 2.401

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