Cozzi R, Attanasio R, Barausse M, Dallabonzana D, Orlandi P, Da Re N, Branca V, Oppizzi G, Gelli D
Division of Endocrinology, Ospedale Niguarda, Milano, Italy.
Eur J Endocrinol. 1998 Nov;139(5):516-21. doi: 10.1530/eje.0.1390516.
Eighteen active acromegalics entered a prospective open study with cabergoline (CAB), a dopaminergic drug much more potent than bromocriptine (Br).
CAB was administered for 6 months at doses ranging between 0.5 mg twice weekly and 0.5 mg/day. Clinical-anamnestic characteristics of the patients were: (i) sensitivity to dopamine agonist drugs (10 patients); (ii) resistance to somatostatin analogs (SAs) (8 patients): (iii) intolerance to SA (3 patients). In 2 patients marked hyperprolactinemia was present.
Basal GH was 6.6 microg/l (2.2-50) (median (range)), and on treatment it was 3.5 microg/l (1.2-34) (P=0.013). The corresponding IGF-I values were 720 microg/l (410-1438) and 375 microg/l (167-1260) respectively (P=0.00001). Individual GH levels decreased below 2 microg/l in 5 patients, and between 2 and 5 microg/l in another 5 patients. IGF-I levels were suppressed below 50% of baseline in 8 patients and normal age-adjusted IGF-I values were reached in 5 patients (27% of the series). The retrospective comparison with previous chronic treatment with Br in the 10 suitable patients showed a greater effectiveness of CAB (IGF-I decrease on CAB treatment, 46.8%, on Br treatment, 31%, P=0.02). Adenoma shrank in the 3 patients whose pituitary imaging was repeated during CAB.
These results envisage that CAB may represent a worthy therapeutic tool in acromegalic patients, inducing a degree of IGF-I and GH suppression comparable to SAs, administered by the oral route and much less expensive.
18例活动性肢端肥大症患者进入一项关于卡麦角林(CAB)的前瞻性开放研究,卡麦角林是一种比溴隐亭(Br)效力更强的多巴胺能药物。
卡麦角林以每周两次0.5毫克至每日0.5毫克的剂量给药6个月。患者的临床 - 病史特征为:(i)对多巴胺激动剂药物敏感(10例患者);(ii)对生长抑素类似物(SAs)耐药(8例患者);(iii)对SAs不耐受(3例患者)。2例患者存在明显的高催乳素血症。
基础生长激素(GH)为6.6微克/升(2.2 - 50)(中位数(范围)),治疗后为3.5微克/升(1.2 - 34)(P = 0.013)。相应的胰岛素样生长因子 - I(IGF - I)值分别为720微克/升(410 - 1438)和375微克/升(167 - 1260)(P = 0.00001)。5例患者的个体GH水平降至2微克/升以下,另外5例患者的GH水平在2至5微克/升之间。8例患者的IGF - I水平被抑制至基线的50%以下,5例患者达到了年龄调整后的正常IGF - I值(占该系列的27%)。对10例合适患者与先前使用溴隐亭的慢性治疗进行回顾性比较,结果显示卡麦角林的疗效更佳(卡麦角林治疗时IGF - I降低46.8%,溴隐亭治疗时降低31%,P = 0.02)。在卡麦角林治疗期间对3例患者重复进行垂体成像,发现腺瘤缩小。
这些结果表明,卡麦角林可能是肢端肥大症患者一种有价值的治疗工具,可诱导与生长抑素类似物相当程度的IGF - I和GH抑制,通过口服给药且成本低得多。