Glucose homeostasis and safety in patients with acromegaly converted from long-acting octreotide to pegvisomant

Glucose homeostasis and safety in patients with acromegaly converted from long-acting octreotide to pegvisomant
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DOI:
10.1210/jc.2005-0331
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发表时间:
2005-10-01
影响因子:
5.8
通讯作者:
Vance, ML
Vance, ML
中科院分区:
医学2区
文献类型:
--
作者:
Barkan, AL;Burman, P;Vance, ML

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背景:在临床实践中,肢端肥大症患者可能会从长效生长抑素类似物治疗转向pegvisomant。改变治疗方法对葡萄糖稳态和安全性的影响尚未报道。目的:本研究的目的是监测igf - 1水平、血糖控制和安全性的变化,特别是肝功能和肿瘤大小。设计:这是一项多中心、开放标签、32周的试验研究。环境:研究在门诊进行。患者:53例既往接受奥曲肽长效释放(LAR)治疗的肢端肥大症患者参加了本研究。干预:Pegvisomant (10mg /d)在最后一次奥曲肽LAR治疗后第4周开始,并根据第12、20和28周的血清IGF-I浓度进行调整。主要结局指标:主要结局指标为转化后前12周IGF-I、糖化血红蛋白A(1c) (HbA(1c))、空腹血糖和安全性的变化。结果:在pegvisomant治疗结束时,78%的患者IGF-I恢复正常。在第32周,中位空腹葡萄糖浓度和HbA(1c)分别降低(-1.4 mmol/l和-0.4%)
Context: In clinical practice, patients with acromegaly may be switched from therapy with long-acting somatostatin analogs to pegvisomant. The effect of changing therapies on glucose homeostasis and safety has not been reported.Objectives: The objectives of this study were to monitor changes in IGF-I levels, glycemic control, and safety, particularly liver function and tumor size.Design: This was a multicenter, open-label, 32-wk trial study.Setting: The study was performed at outpatient clinics.Patients: Fifty-three patients with acromegaly previously treated with octreotide long-acting release (LAR) participated in this study.Intervention: Pegvisomant (10 mg/d) was initiated 4 wk after the last dose of octreotide LAR and was adjusted based on serum IGF-I concentrations at wk 12, 20, and 28.Main Outcome Measures: The main outcome measures were changes in IGF-I, glycosylated hemoglobin A(1c) (HbA(1c)), fasting plasma glucose, and safety during the first 12 wk after conversion.Results: At the end of pegvisomant treatment, IGF-I was normalized in 78% of patients. At wk 32, median fasting glucose concentration and HbA(1c) were reduced (-1.4 mmol/liter and -0.4%, respectively; both P