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催乳素瘤的药物治疗。

Medical therapy of prolactinomas.

作者信息

Jaquet P

机构信息

Service d'Endocrinologie, CHU Nord, Marseille, France.

出版信息

Acta Endocrinol (Copenh). 1993 Jul;129 Suppl 1:31-3.

PMID:8103957
Abstract

Bromocriptine therapy normalizes prolactin levels and restores fertility in 82 to 90% of patients with prolactinoma. Tumour diameter is reduced (> 25%) in 60 to 79% of patients within 3 to 12 months. Symptoms return in the majority of cases, even after 1.5 to 10 years of treatment, if the drug is withdrawn; thus, in macroprolactinoma, life-long dopamine agonist treatment is indicated. A depot formulation of bromocriptine has been introduced which allows 50 to 100 mg of bromocriptine to be administered at monthly intervals. Treatment resulted in normalization of prolactin levels in 72% of cases and a tumour shrinkage (> 25%) was noted in 54%. This preparation is well tolerated, apart from initial injection. CV 205-502 is a non-ergot long-acting dopamine agonist. A daily dose of 75 to 400 micrograms reduced hyperprolactinaemia in 58 to 91% of patients and induced tumour shrinkage in 52%. CV 205-502 achieved normal prolactin levels in 50% of patients previously diagnosed as bromocriptine-resistant. Cabergoline is an ergot derivative. A twice weekly dose of 0.2 to 3.5 mg induced tumour shrinkage in 96% of patients treated. Pergolide is another potent dopamine agonist and is expected to give similar results to cabergoline and CV 205-502.

摘要

溴隐亭疗法可使82%至90%的催乳素瘤患者催乳素水平恢复正常并恢复生育能力。60%至79%的患者在3至12个月内肿瘤直径缩小(>25%)。在大多数情况下,即使经过1.5至10年的治疗,如果停药,症状仍会复发;因此,对于大催乳素瘤,建议进行终身多巴胺激动剂治疗。已推出溴隐亭长效注射剂,允许每月注射50至100毫克溴隐亭。治疗使72%的患者催乳素水平恢复正常,54%的患者肿瘤缩小(>25%)。除了初次注射外,这种制剂耐受性良好。CV 205-502是一种非麦角长效多巴胺激动剂。每日剂量75至400微克可使58%至91%的患者高催乳素血症得到缓解,52%的患者肿瘤缩小。CV 205-502使50%先前诊断为对溴隐亭耐药的患者催乳素水平恢复正常。卡麦角林是一种麦角衍生物。每周两次剂量0.2至3.5毫克可使96%接受治疗的患者肿瘤缩小。培高利特是另一种强效多巴胺激动剂,预计会产生与卡麦角林和CV 205-502相似的效果。

相似文献

1
Medical therapy of prolactinomas.催乳素瘤的药物治疗。
Acta Endocrinol (Copenh). 1993 Jul;129 Suppl 1:31-3.
2
[Treatment of prolactinoma with a new dopamine agonist].[新型多巴胺激动剂治疗泌乳素瘤]
Dtsch Med Wochenschr. 1991 Aug 16;116(33):1224-7. doi: 10.1055/s-2008-1063739.
3
Diagnosis and drug therapy of prolactinoma.泌乳素瘤的诊断与药物治疗
Drugs. 1996 Jun;51(6):954-65. doi: 10.2165/00003495-199651060-00004.
4
Endocrine function, psychiatric and clinical consequences in patients with macroprolactinomas after long-term treatment with the new non-ergot dopamine agonist CV205-502.新型非麦角多巴胺激动剂CV205-502长期治疗大泌乳素瘤患者后的内分泌功能、精神及临床后果
Q J Med. 1991 Nov;81(295):891-906.
5
Treatment of macroprolactinoma with the new potent non-ergot D2-dopamine agonist quinagolide and effects on prolactin levels, pituitary function, an the renin-aldosterone system. Results of a clinical long-term study.新型强效非麦角D2-多巴胺激动剂喹高利特治疗大泌乳素瘤及其对催乳素水平、垂体功能和肾素-醛固酮系统的影响。一项临床长期研究结果
Arzneimittelforschung. 1993 Apr;43(4):421-5.
6
Effect of the new dopaminergic agonist CV 205-502 on plasma prolactin levels and tumour size in bromocriptine-resistant prolactinomas.新型多巴胺能激动剂CV 205-502对溴隐亭抵抗性催乳素瘤患者血浆催乳素水平及肿瘤大小的影响
Clin Endocrinol (Oxf). 1991 Jan;34(1):25-9. doi: 10.1111/j.1365-2265.1991.tb01731.x.
7
Criteria for medical as opposed to surgical treatment of prolactinomas.泌乳素瘤的药物治疗而非手术治疗标准。
Acta Endocrinol (Copenh). 1993 Jul;129 Suppl 1:27-30.
8
Long-term treatment of bromocriptine-intolerant prolactinoma patients with CV 205-502.用CV 205-502对溴隐亭不耐受的泌乳素瘤患者进行长期治疗。
J Reprod Med. 1994 Jun;39(6):449-54.
9
The use of surgery for the treatment of prolactinomas.手术在泌乳素瘤治疗中的应用。
Acta Endocrinol (Copenh). 1993 Jul;129 Suppl 1:34-7.
10
[The best approach to treat prolactinoma].[治疗泌乳素瘤的最佳方法]
Gac Med Mex. 2004 Sep-Oct;140(5):567-9.

引用本文的文献

1
Pituitary Adenomas.垂体腺瘤
Curr Treat Options Neurol. 2002 Jul;4(4):261-269. doi: 10.1007/s11940-002-0026-0.
2
Pituitary tumor diagnosis and treatment.垂体瘤的诊断与治疗。
Curr Neurol Neurosci Rep. 2002 May;2(3):236-45. doi: 10.1007/s11910-002-0082-6.
3
Pituitary adenomas secreting large amounts of prolactin may give false low values in immunoradiometric assays. The hook effect.分泌大量催乳素的垂体腺瘤在免疫放射分析中可能会给出错误的低值。钩状效应。
J Endocrinol Invest. 1998 Mar;21(3):184-8. doi: 10.1007/BF03347299.