Literature DB >> 11081177

New medical treatment for acromegaly.

A J van der Lely1, W W de Herder, S W Lamberts.   

Abstract

The available somatostatin analogs for subcutaneous administration lower growth hormone (GH) levels in more than 90% of patients and Insulin-like growth factor-I (IGF-I) levels in up to 60%. They are also capable of reducing tumor size in up to 50%. Recently long-acting somatostatin analogs were introduced. The use of these application forms can result in normalization of IGF-1 in 60% of patients after 1 year and in 75% after 3 years. The development of selective analogs for the somatostatin receptor subtype-5 potentially will enhance the potency and the spectrum of the medical treatment of acromegaly with somatostatin analogs. The new generation of dopaminergic drugs also form a potentially effective and well tolerated therapy that should be considered in the management of those acromegalic patients, which have relative low serum IGF-I concentrations, along with high serum prolactine levels. Finally, growth hormone receptor (GHR) antagonists are under development for the use in humans. Preliminary results look promising, when biochemical parameters are concerned. Interim analysis of a phase 3 study with B2036-PEG in 38 patients does show that normalization of IGF-I concentrations is reached in at least 92% of the treated patients.

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Year:  1999        PMID: 11081177     DOI: 10.1023/a:1009930223314

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


  35 in total

1.  Evidence for dopamine agonists in the treatment of acromegaly.

Authors:  P Jaquet
Journal:  J Endocrinol       Date:  1997-10       Impact factor: 4.286

2.  Prolactinomas apparently resistant to quinagolide respond to cabergoline therapy.

Authors:  A Colao; G Lombardi
Journal:  J Clin Endocrinol Metab       Date:  1997-08       Impact factor: 5.958

3.  Treatment of macroprolactinoma with cabergoline: a study of 85 patients.

Authors:  C I Ferrari; R Abs; J S Bevan; G Brabant; E Ciccarelli; T Motta; M Mucci; M Muratori; L Musatti; G Verbessem; M F Scanlon
Journal:  Clin Endocrinol (Oxf)       Date:  1997-04       Impact factor: 3.478

Review 4.  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

Review 5.  The role of somatostatin agonistic analogs in the treatment of acromegaly.

Authors:  G Tolis
Journal:  Metabolism       Date:  1996-08       Impact factor: 8.694

6.  Somatostatin receptor (SSTR) subtype-selective analogues differentially suppress in vitro growth hormone and prolactin in human pituitary adenomas. Novel potential therapy for functional pituitary tumors.

Authors:  I Shimon; X Yan; J E Taylor; M H Weiss; M D Culler; S Melmed
Journal:  J Clin Invest       Date:  1997-11-01       Impact factor: 14.808

7.  Sandostatin LAR in acromegalic patients: long-term treatment.

Authors:  A K Fløgstad; J Halse; S Bakke; I Lancranjan; P Marbach; C Bruns; J Jervell
Journal:  J Clin Endocrinol Metab       Date:  1997-01       Impact factor: 5.958

8.  The efficacy and tolerability of CV 205-502 (a nonergot dopaminergic drug) in macroprolactinoma patients and in prolactinoma patients intolerant to bromocriptine.

Authors:  A J van der Lely; J Brownell; S W Lamberts
Journal:  J Clin Endocrinol Metab       Date:  1991-05       Impact factor: 5.958

9.  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

10.  Dose-dependent suppression of serum prolactin by cabergoline in hyperprolactinaemia: a placebo controlled, double blind, multicentre study. European Multicentre Cabergoline Dose-finding Study Group.

Authors:  J Webster; G Piscitelli; A Polli; A D'Alberton; L Falsetti; C Ferrari; P Fioretti; G Giordano; M L'Hermite; E Ciccarelli
Journal:  Clin Endocrinol (Oxf)       Date:  1992-12       Impact factor: 3.478

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  2 in total

1.  Poor responses to a test dose of subcutaneous octreotide predict the need for adjuvant therapy to achieve 'safe' growth hormone levels.

Authors:  J R Lindsay; E M McConnell; S J Hunter; D R McCance; B Sheridan; A B Atkinson
Journal:  Pituitary       Date:  2004       Impact factor: 4.107

2.  Somatotroph pituitary adenoma with acromegaly and autosomal dominant polycystic kidney disease: SSTR5 polymorphism and PKD1 mutation.

Authors:  Luis V Syro; Jamie L Sundsbak; Bernd W Scheithauer; Rodrigo A Toledo; Mauricio Camargo; Christina M Heyer; Tomoko Sekiya; Humberto Uribe; Jorge I Escobar; Martin Vasquez; Fabio Rotondo; Sergio P A Toledo; Kalman Kovacs; Eva Horvath; Dusica Babovic-Vuksanovic; Peter C Harris
Journal:  Pituitary       Date:  2012-09       Impact factor: 4.107

  2 in total

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