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

作者信息

De Luis D A, Becerra A, Lahera M, Botella J I, Varela C

机构信息

Institute of Endocrinology and Nutrition, Medicine School, Valladolid, Spain.

出版信息

J Endocrinol Invest. 2000 Jul-Aug;23(7):428-34. doi: 10.1007/BF03343751.

DOI:10.1007/BF03343751
PMID:11005266
Abstract

Quinagolide (QUI) and cabergoline (CAB) are dopamine agonists recently introduced for the treatment of hyperprolactinemia. In the present study, these drugs have been compared in terms of effectiveness and tolerability. Twenty patients (18 females and 2 males) with hyperprolactinemia (8 with microprolactinomas, 6 with idiopathic hyperprolactinemia and 6 with empty sella turcica syndrome) were treated with oral QUI (75 microg once daily) and CAB (0,5 mg twice weekly), in a randomized cross-over trial with placebo between both drugs. Each drug was administered for 12 weeks, separated by other 12 weeks with placebo. PRL levels decreased with both drugs at 2 or 4 weeks of starting the treatment, without differences between both drugs at weeks 4, 8 and 12. At week 12, normal PRL levels (<20 ng/ml) were attained in 90% patients with CAB and only in 75% patients with QUI (p<0.05). After discontinuation of treatment, significant increase in serum PRL was higher after QUI withdrawal than after CAB. Clinical efficacy of both treatments was similar in terms of improvement amenorrhea, oligomenorrhea, galactorrhea, and impotence. All patients completed both cycles of treatment, and the most frequent side-effects were nausea, headache and dizziness, without significant differences between CAB (30%) and QUI (55%). Our study indicates that, at the doses employed here, CAB showed a high percentage of patients with normal PRL at the end of treatment and long-lasting efficacy in the levels of PRL. Clinical response and side-effects were similar in both drugs.

摘要

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The efficacy and safety of quinagolide in hyperprolactinemia treatment: A systematic review and meta-analysis.

本文引用的文献

1
Prolactinomas resistant to standard dopamine agonists respond to chronic cabergoline treatment.对标准多巴胺激动剂耐药的泌乳素瘤对长期卡麦角林治疗有反应。
J Clin Endocrinol Metab. 1997 Mar;82(3):876-83. doi: 10.1210/jcem.82.3.3822.
2
Treatment of prolactin-secreting macroadenomas with the once-weekly dopamine agonist cabergoline.使用每周一次的多巴胺激动剂卡麦角林治疗分泌催乳素的大腺瘤。
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Comparison among different dopamine-agonists of new formulation in the clinical management of macroprolactinomas.
喹高利特治疗高泌乳素血症的疗效和安全性:系统评价和荟萃分析。
Front Endocrinol (Lausanne). 2023 Jan 24;14:1027905. doi: 10.3389/fendo.2023.1027905. eCollection 2023.
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Medical treatment of prolactinomas.催乳素瘤的治疗。
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Diagnosis and management of hyperprolactinemia.高催乳素血症的诊断与管理
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Clinical pharmacokinetics of cabergoline.卡麦角林的临床药代动力学
Clin Pharmacokinet. 2003;42(7):633-45. doi: 10.2165/00003088-200342070-00003.
新型制剂中不同多巴胺激动剂在大泌乳素瘤临床管理中的比较。
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A cross-over study with the two novel dopaminergic drugs cabergoline and quinagolide in hyperprolactinemic patients.一项针对高泌乳素血症患者,使用两种新型多巴胺能药物卡麦角林和喹高利特的交叉研究。
J Endocrinol Invest. 1994 Jan;17(1):51-7. doi: 10.1007/BF03344963.
5
The effects of CV205-502 in patients with hyperprolactinaemia intolerant and/or resistant to bromocriptine.CV205-502对不耐受和/或对溴隐亭耐药的高泌乳素血症患者的影响。
Horm Res. 1993;39(5-6):218-22. doi: 10.1159/000182739.
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Drugs five years later. Bromocriptine.五年后的药物。溴隐亭。
Ann Intern Med. 1984 Jan;100(1):78-91. doi: 10.7326/0003-4819-100-1-78.
7
Bromocriptine as primary therapy for prolactin-secreting macroadenomas: results of a prospective multicenter study.溴隐亭作为分泌催乳素大腺瘤的一线治疗:一项前瞻性多中心研究结果
J Clin Endocrinol Metab. 1985 Apr;60(4):698-705. doi: 10.1210/jcem-60-4-698.
8
Parenteral bromocriptine in the treatment of hormonally active pituitary tumours.胃肠外使用溴隐亭治疗有激素活性的垂体肿瘤。
Clin Endocrinol (Oxf). 1986 May;24(5):505-13. doi: 10.1111/j.1365-2265.1986.tb03279.x.
9
Prolactin-lowering effect of acute and once weekly repetitive oral administration of cabergoline at two dose levels in hyperprolactinemic patients.卡麦角林两种剂量水平急性及每周一次重复口服给药对高泌乳素血症患者的降泌乳素作用
J Clin Endocrinol Metab. 1988 Jan;66(1):193-8. doi: 10.1210/jcem-66-1-193.
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Hormonal effects of CV 205-502, a novel octahydrobenzo [g] quinoline with potent dopamine agonist properties.
Life Sci. 1988;43(17):1355-62. doi: 10.1016/0024-3205(88)90301-3.