QUINAGOLIDE

Manufactured by Sandoz, brand name is Norprolac. In

its earlier days it used to be called CV 205-502 and

additional abstracts may be found in the medical

databases under that name


UI  - 97382038
AU  - Tabarin A; Catargi B
TI  - [Treatment of macroprolactinomas with quinagolide (Norprolac)]
SO  - Ann Endocrinol (Paris) 1997;58(2):87-94
AD  - Departement d'Endocrinologie-Diabetologie, CHU de Bordeaux, Hopital du
      Haut-Leveque, Pessac.
AB  - Quinagolide is a non-ergot dopaminergic agonist recently available on
      the French market. The endocrine and tumoral efficacy as well as the
      safety and tolerability of quinagolide in the treatment of macroprol-
      actinomas are reviewed. In this situation, plasma prolactin levels
      are normalized in about 60% of patients and in about one third of
      those who are resistant to bromocriptine. A significant decrease in
      pituitary tumor size is demonstrated by radiographic studies in 58 to
      69% of patients. About one third of patients show more than 50% tumor
      shrinkage. The tolerability of quinagolide is satisfactory in most
      cases and clearly better than that of bromocriptine. Thus, quinagoli-
      de is a useful tool in the treatment of macroprolactinomas. (30 Refs)


NLM CIT. ID: 92228958
TITLE:   Endocrine function, psychiatric and clinical consequences in patients
         with macroprolactinomas after long-term treatment with the new non-
         ergot dopamine agonist CV205-502.
AUTHORS: Barnett PS; Palazidou E; Miell JP; Coskeran PB
      Butler J; Dawson JM; Maccabe J; McGregor AM
AUTHOR AFFILIATION:
      Department of Medicine, King's College School of Medicine and
      Dentistry, London.
PUBLICATION TYPES:
      JOURNAL ARTICLE
LANGUAGES:
      Eng
REGISTRY NUMBERS:
      0 (Aminoquinolines)
      0 (Dopamine Agents)
      9002-62-4 (Prolactin)
      97805-50-0 (CV 205-502)
ABSTRACT:
      Although bromocriptine is the mainstay of treatment of
      macroprolactinomas, its therapeutic usefulness may be limited by poor
      tolerance, lack of consistent reduction in serum prolactin levels and
      tumour size, and the necessity for multiple dosing. Consequently new
      dopamine agonists have been developed, including the long acting non-
      ergot agonist CV205-502 which has been shown to date to be
      consistently effective in reducing serum PRL levels and causing
      tumour shrinkage. Twelve patients were treated for periods of up to
      24 months with CV205- 502 in doses ranging from 0.075 mg to 1.65 mg
      once daily. Clinical and psychiatric assessments, biochemical
      parameters, tumour size determination, and anterior pituitary
      function tests were performed regularly. Tumour shrinkage was noted
      in all patients, and varied from 11 per cent reduction to complete
      disappearance of tumour. Prolactin levels became normal in seven
      patients and were reduced by more than 90 per cent in the remaining
      five. Normal menstruation resumed in six of the eight women, one of
      whom conceived after one year of therapy; libido returned in all
      patients. Psychiatric complications occurred in three patients
      necessitating withdrawal of therapy in one. Significant weight loss
      was noted in 11 of 12 patients. Triglyceride concentrations fell from
      1.5 +/- 0.1 to 1.0 +/- 0.1 mmol/l at 12 months (p = 0.006), and
      cholesterol fell from 6.3 +/- 0.4 to 5.3 +/- 0.3 mmol/l (p = 0.04).
      The mean TSH response 20 min following TRH injection fell from 14.3
      +/- 2.9 to 8.7 +/- 1.3 mU/l at 2 months (p = 0.027). There was a
      significant increase in the peak growth hormone response to the
      insulin stress test from basal median (25th-75th centiles) values of
      15 (4.4- 25.5) mU/l to 24.5 (9-37) mU/l at 2 months (p less than
      0.01) and 31 (19.3-63.5) at 12 months (p less than 0.005). CV205-502
      is highly effective in the medical management of patients with
      macroprolactinomas, reducing prolactin levels and tumour size and
      restoring normal anterior pituitary function. It is, however,
      associated with the important side effects of weight loss and
      psychiatric complications which should be drawn to the attention of
      clinicians.
MAIN MESH HEADINGS:
      Aminoquinolines/*therapeutic use
      Dopamine Agents/*therapeutic use
      Pituitary Gland, Anterior/*physiopathology
      Pituitary Neoplasms/*drug therapy
      Prolactinoma/*drug therapy
ADDITIONAL MESH HEADINGS:
      Adult
      Aminoquinolines/adverse effects
      Dopamine Agents/adverse effects
      Female
      Human
      Male
      Mental Disorders/chemically induced
      Middle Age
      Pituitary Neoplasms/pathology
      Pituitary Neoplasms/physiopathology
      Prolactin/blood
      Prolactinoma/pathology
      Prolactinoma/physiopathology
      Support, Non-U.S. Gov't
      Weight Loss/drug effects
NLM PUBMED CIT. ID:
      1687293
SOURCE:  Q J Med 1991 Nov;81(295):891-906

Return to my Treatment of Prolactinomas page

This Page Last Updated on 6th. July, 2000