Literature DB >> 25677539

Medical Treatment of Acromegaly with Dopamine Agonists or Somatostatin Analogs.

Philippe Chanson1.   

Abstract

Treatment of acromegaly aims to correct (or prevent) tumor compression of surrounding tissues by excising the disease-causing lesion and reduce growth hormone (GH) and IGF-1 levels to normal values. When surgery (the usual first-line treatment) fails to correct GH/IGF-1 hypersecretion, medical treatment with dopamine agonists (DAs; particularly cabergoline) or somatostatin analogs (SAs) can be used. The GH receptor antagonist pegvisomant is helpful in patients who are totally or partially resistant to SAs and can be given in association with both SAs and/or DAs. Thanks to this multistep therapeutic strategy, adequate hormonal disease control is achieved in most patients, giving them normal life expectancy. Comorbidities associated with acromegaly generally improve after treatment, but persistent sequelae may nonetheless impair quality of life.
© 2015 S. Karger AG, Basel.

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Year:  2015        PMID: 25677539     DOI: 10.1159/000377704

Source DB:  PubMed          Journal:  Neuroendocrinology        ISSN: 0028-3835            Impact factor:   4.914


  9 in total

Review 1.  Acromegalic cardiomyopathy: Epidemiology, diagnosis, and management.

Authors:  Ajay N Sharma; Marilyn Tan; Ezra A Amsterdam; Gagan D Singh
Journal:  Clin Cardiol       Date:  2018-03-25       Impact factor: 2.882

2.  Prescription patterns of somatostatin analogs in patients with acromegaly and neuroendocrine tumors.

Authors:  J E Machado-Alba; M E Machado-Duque; A Gaviria-Mendoza; I N Arsof-Saab; C A Castellanos-Moreno; L Botero; L Triana
Journal:  J Endocrinol Invest       Date:  2022-08-01       Impact factor: 5.467

Review 3.  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

Review 4.  Hyperglycemia induced by pasireotide in patients with Cushing's disease or acromegaly.

Authors:  Julie M Silverstein
Journal:  Pituitary       Date:  2016-10       Impact factor: 4.107

5.  Safety and tolerability of pasireotide long-acting release in acromegaly-results from the acromegaly, open-label, multicenter, safety monitoring program for treating patients who have a need to receive medical therapy (ACCESS) study.

Authors:  Maria Fleseriu; Elisha Rusch; Eliza B Geer
Journal:  Endocrine       Date:  2016-11-28       Impact factor: 3.633

6.  Exploration of Somatostatin Binding Mechanism to Somatostatin Receptor Subtype 4.

Authors:  Rita Börzsei; Balázs Zoltán Zsidó; Mónika Bálint; Zsuzsanna Helyes; Erika Pintér; Csaba Hetényi
Journal:  Int J Mol Sci       Date:  2022-06-21       Impact factor: 6.208

Review 7.  Hormone supply to the pituitary gland: A comprehensive investigation of female‑related tumors (Review).

Authors:  Wenxiu Tian; Huimin Qi; Zhimei Wang; Sen Qiao; Ping Wang; Junhong Dong; Hongmei Wang
Journal:  Int J Mol Med       Date:  2022-08-10       Impact factor: 5.314

8.  In vitro impact of pegvisomant on growth hormone-secreting pituitary adenoma cells.

Authors:  Thomas Cuny; Caroline Zeiller; Martin Bidlingmaier; Céline Défilles; Catherine Roche; Marie-Pierre Blanchard; Marily Theodoropoulou; Thomas Graillon; Morgane Pertuit; Dominique Figarella-Branger; Alain Enjalbert; Thierry Brue; Anne Barlier
Journal:  Endocr Relat Cancer       Date:  2016-06-07       Impact factor: 5.678

9.  Pegvisomant in combination or pegvisomant alone after failure of somatostatin analogs in acromegaly patients: an observational French ACROSTUDY cohort study.

Authors:  Emmanuelle Kuhn; Philippe Caron; Brigitte Delemer; Isabelle Raingeard; Hervé Lefebvre; Gérald Raverot; Christine Cortet-Rudelli; Rachel Desailloud; Clementine Geffroy; Robin Henocque; Yves Brault; Thierry Brue; Philippe Chanson
Journal:  Endocrine       Date:  2020-09-28       Impact factor: 3.633

  9 in total

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