CV205–502, A NEW NON-ERGOT DOPAMINE AGONIST, REDUCES PROLACTINOMA SIZE IN MAN
Autor: | J. J. Maccabe, P. S. Barnett, Joan Butler, Alan McGregor, J. M. Dawson, Patsy Coskeran |
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Rok vydání: | 1990 |
Předmět: |
Adult
Male Agonist medicine.medical_specialty Adenoma medicine.drug_class Endocrinology Diabetes and Metabolism Dopamine Agents Dopamine agonist Endocrinology Dopamine Internal medicine medicine Humans Pituitary Neoplasms Prolactinoma business.industry Middle Aged medicine.disease Prolactin Bromocriptine Discontinuation Aminoquinolines Female Tomography X-Ray Computed business medicine.drug |
Zdroj: | Clinical Endocrinology. 33:307-316 |
ISSN: | 1365-2265 0300-0664 |
Popis: | Seven patients with large prolactin-secreting pituitary adenomas were treated for 8 weeks with once-daily doses of the new, potent, non-ergot, long-acting dopamine agonist CV205-502. In five patients previous treatment with bromocriptine had failed to control their disease or been poorly tolerated and had therefore ceased. In all seven patients serum prolactin levels fell over the 8-week period of CV205-502 treatment with the decrease ranging from 33 to 99%. Associated with this decline in prolactin all patients showed symptomatic improvement with two of the five women beginning to menstruate and the two patients with visual field impairment showing marked improvement. Tolerance of the drug, with doses at 8 weeks ranging from 0.075 to 0.3 mg, was excellent with only minimal and transient side-effects being noted in three patients in none of whom was discontinuation of therapy necessary. In one patient noncompliance after 6 weeks of therapy was associated with a rapid return of her serum prolactin towards pretreatment levels. In all seven patients the clinical and biochemical improvement was accompanied by a marked reduction in tumour size. |
Databáze: | OpenAIRE |
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