Barnett P S, Palazidou E, Miell J P, Coskeran P B, Butler J, Dawson J M, Maccabe J, McGregor A M
Department of Medicine, King's College School of Medicine and Dentistry, London.
Q J Med. 1991 Nov;81(295):891-906.
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.
尽管溴隐亭是治疗大泌乳素瘤的主要药物,但其治疗效果可能受到耐受性差、血清泌乳素水平和肿瘤大小缺乏持续降低以及需要多次给药的限制。因此,已开发出新型多巴胺激动剂,包括长效非麦角激动剂CV205 - 502,迄今为止已证明其在降低血清泌乳素水平和使肿瘤缩小方面始终有效。12例患者接受CV205 - 502治疗长达24个月,每日剂量范围为0.075毫克至1.65毫克。定期进行临床和精神评估、生化参数测定、肿瘤大小测定以及垂体前叶功能测试。所有患者均出现肿瘤缩小,缩小幅度从11%到肿瘤完全消失不等。7例患者的泌乳素水平恢复正常,其余5例患者的泌乳素水平降低超过90%。8名女性中有6名恢复正常月经,其中1名在治疗1年后怀孕;所有患者的性欲均恢复。3例患者出现精神并发症,其中1例需要停药。12例患者中有11例出现明显体重减轻。甘油三酯浓度在12个月时从1.5±0.1毫摩尔/升降至1.0±0.1毫摩尔/升(p = 0.006),胆固醇从6.3±0.4毫摩尔/升降至5.3±0.3毫摩尔/升(p = 0.04)。促甲状腺激素释放激素注射后20分钟的平均促甲状腺激素反应在2个月时从14.3±2.9毫国际单位/升降至8.7±1.3毫国际单位/升(p = 0.027)。胰岛素应激试验的生长激素峰值反应从基础中位数(第25 - 75百分位数)值15(4.4 - 25.5)毫国际单位/升在2个月时显著增加至24.5(9 - 37)毫国际单位/升(p < 0.01),在12个月时增加至31(19.3 - 63.5)毫国际单位/升(p < 0.005)。CV205 - 502在大泌乳素瘤患者的药物治疗中非常有效,可降低泌乳素水平和肿瘤大小并恢复正常垂体前叶功能。然而,它与体重减轻和精神并发症等重要副作用相关,临床医生应予以关注。