Literature DB >> 2570790

Effectiveness and tolerability of long term treatment with cabergoline, a new long-lasting ergoline derivative, in hyperprolactinemic patients.

E Ciccarelli1, M Giusti, C Miola, F Potenzoni, D Sghedoni, F Camanni, G Giordano.   

Abstract

Cabergoline (CAB) is a new oral dopaminergic compound showing a very long-lasting PRL-lowering activity and reported to be well tolerated. The efficacy and tolerability of chronic treatment with CAB in 30 female hyperprolactinemic patients, aged 18-52 yr (6 microadenomas, 3 macroadenomas, and 21 functional hyperprolactinemias), were studied. In a group of 10 patients who received CAB (0.8 mg once weekly or 0.4 mg twice weekly) for 8 weeks PRL levels normalized while on treatment and remained normal (8 patients) or greatly reduced (1 patient) for 1-2 months after discontinuation of the drug. Twenty-six patients underwent chronic treatment (6-12 months) with an initial dose of 0.5 mg once weekly, subsequently increased to 1-2 mg in 10 patients and decreased in the other 2. Due to severe side-effects CAB was discontinued in 3 patients, in 1, 8, and 12 weeks. A significant reduction of PRL levels was already observed after the first week of treatment (mean +/- SEM basal values, 90.1 +/- 13.3 vs. 29.5 +/- 6.3 micrograms/L; P less than 0.001). Twenty-two patients had normal PRL levels in 1-36 weeks (mean, 6 weeks) with 0.5-2 mg CAB. Twenty-two patients resumed regular menses; 2 patients became pregnant after 3-11 months of treatment. Thirteen patients complained of side-effects (nausea, hypotension, headache, gastric pain, dizziness, and weakness) that disappeared with time in 10 of them. The comparison with a previous bromocriptine treatment regimen in 20 patients had shown that the number of patients requiring discontinuation of the latter drug was significantly higher (7 vs. 3 patients; P less than 0.001). However, 2 patients who needed to discontinue CAB were able to tolerate bromocriptine therapy. A computed tomographic scan performed after 12 months of therapy in 7 patients showed a significant reduction (50%) of the adenoma in 5. In conclusion, our results show that CAB is a well tolerated new dopamine agonist with long-lasting activity that represents an advance in chronic medical treatment of hyperprolactinemic conditions.

Entities:  

Mesh:

Substances:

Year:  1989        PMID: 2570790     DOI: 10.1210/jcem-69-4-725

Source DB:  PubMed          Journal:  J Clin Endocrinol Metab        ISSN: 0021-972X            Impact factor:   5.958


  13 in total

Review 1.  Medical management of prolactin-secreting pituitary adenomas.

Authors:  Mark E Molitch
Journal:  Pituitary       Date:  2002       Impact factor: 4.107

Review 2.  Effects of cabergoline on pregnancy and embryo-fetal development: retrospective study on 103 pregnancies and a review of the literature.

Authors:  Graciela Stalldecker; María Susana Mallea-Gil; Mirtha Guitelman; Analía Alfieri; María Carolina Ballarino; Laura Boero; Alberto Chervin; Karina Danilowicz; Sabrina Diez; Patricia Fainstein-Day; Natalia García-Basavilbaso; Mariela Glerean; Viviana Gollan; Débora Katz; Mónica Graciela Loto; Marcos Manavela; Amelia Susana Rogozinski; Marisa Servidio; Nicolás Marcelo Vitale
Journal:  Pituitary       Date:  2010-12       Impact factor: 4.107

Review 3.  A comparative review of the tolerability profiles of dopamine agonists in the treatment of hyperprolactinaemia and inhibition of lactation.

Authors:  J Webster
Journal:  Drug Saf       Date:  1996-04       Impact factor: 5.606

4.  Long-term treatment with cabergoline, a new long-lasting ergoline derivate, in idiopathic or tumorous hyperprolactinaemia and outcome of drug-induced pregnancy.

Authors:  E Ciccarelli; S Grottoli; P Razzore; D Gaia; A Bertagna; S Cirillo; T Cammarota; M Camanni; F Camanni
Journal:  J Endocrinol Invest       Date:  1997-10       Impact factor: 4.256

5.  Cabergoline: a first-choice treatment in patients with previously untreated prolactin-secreting pituitary adenoma.

Authors:  S Cannavò; L Curtò; S Squadrito; B Almoto; A Vieni; F Trimarchi
Journal:  J Endocrinol Invest       Date:  1999-05       Impact factor: 4.256

6.  A randomized cross-over study comparing cabergoline and quinagolide in the treatment of hyperprolactinemic patients.

Authors:  D A De Luis; A Becerra; M Lahera; J I Botella; C Varela
Journal:  J Endocrinol Invest       Date:  2000 Jul-Aug       Impact factor: 4.256

7.  Cabergoline as a first-line treatment in newly diagnosed macroprolactinomas.

Authors:  N Pontikides; G E Krassas; E Nikopoulou; T Kaltsas
Journal:  Pituitary       Date:  2000-05       Impact factor: 4.107

Review 8.  Cabergoline. A review of its pharmacological properties and therapeutic potential in the treatment of hyperprolactinaemia and inhibition of lactation.

Authors:  C P Rains; H M Bryson; A Fitton
Journal:  Drugs       Date:  1995-02       Impact factor: 9.546

9.  A cross-over study with the two novel dopaminergic drugs cabergoline and quinagolide in hyperprolactinemic patients.

Authors:  M Giusti; E Porcella; A Carraro; M Cuttica; S Valenti; G Giordano
Journal:  J Endocrinol Invest       Date:  1994-01       Impact factor: 4.256

10.  Treatment of prolactinoma patients with the new non-ergot dopamine agonist roxindol: first results.

Authors:  C Jaspers; G Benker; D Reinwein
Journal:  Clin Investig       Date:  1994-06
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.