首页> 外文期刊>Pituitary >Rapid and sustained reduction of serum growth hormone and insulin-like growth factor-1 in patients with acromegaly receiving lanreotide Autogel therapy: a randomized, placebo-controlled, multicenter study with a 52 week open extension.
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Rapid and sustained reduction of serum growth hormone and insulin-like growth factor-1 in patients with acromegaly receiving lanreotide Autogel therapy: a randomized, placebo-controlled, multicenter study with a 52 week open extension.

机译:接受兰瑞肽Autogel治疗的肢端肥大症患者的血清生长激素和胰岛素样生长因子-1持续快速降低:一项随机,安慰剂对照,多中心研究,开放期延长52周。

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The study was designed to evaluate the long-term efficacy and safety of the 28-day prolonged-release Autogel formulation of the somatostatin analogue lanreotide (Lan-Autogel) in unselected patients with acromegaly. The study comprised four phases: washout; a double-blind comparison with placebo, at a single randomized dose (60, 90 or 120 mg) of Lan-Autogel; a single-blind, fixed-dose phase for four injections (placebo group was re-allocated to active treatment); and eight injections with doses tailored according to biochemical response. Serum samples were assessed for growth hormone (GH) and insulin-like growth factor-1 (IGF-1) levels, at weeks 4, 13, 14, 15, 16, 32 and 52. 108 patients were enrolled and 99 completed 52 weeks' treatment. Four weeks after the first injection, serum GH levels decreased by >50% from baseline in 63% of patients receiving Lan-Autogel compared with 0% receiving placebo (P < 0.001). After four injections, 72% of patients had a >50% reduction in GH levels; 49% patients achieved GH levels < or = 2.5 ng/ml; 54% had normalized IGF-1; and 38% achieved the combined criterion of GH level < or = 2.5 ng/ml and normalized IGF-1. The corresponding proportions by week 52 were 82, 54, 59 and 43%, respectively. In patients not requiring dose escalation to 120 mg, 85% achieved biochemical control (combined criterion). Treatment was well tolerated by all patients. In conclusion, Lan-Autogel was effective in controlling GH and IGF-1 hypersecretion in patients with acromegaly and showed a rapid onset of action.
机译:该研究旨在评估生长抑素类似物兰瑞肽(Lan-Autogel)的28天长效Autogel制剂在未选定的肢端肥大症患者中的长期疗效和安全性。该研究包括四个阶段:冲刷阶段;冲刷阶段。 Lan-Autogel单次随机剂量(60、90或120 mg)与安慰剂的双盲比较;单盲,固定剂量阶段,共四次注射(安慰剂组被重新分配给积极治疗);根据生化反应调整剂量的八次注射。在第4、13、14、15、16、32和52周时评估血清样本的生长激素(GH)和类胰岛素生长因子-1(IGF-1)水平。招募了108位患者,其中99位完成了52周治疗。首次注射后四周,接受Lan-Autogel的患者中63%的患者血清GH水平较基线降低了50%以上,而接受安慰剂的患者则为0%(P <0.001)。在四次注射后,72%的患者GH水平降低了> 50%。 49%的患者达到GH水平≤2.5 ng / ml; 54%的人将IGF-1标准化; 38%的人达到了GH水平≤2.5 ng / ml和归一化的IGF-1的综合标准。到第52周的相应比例分别为82%,54、59和43%。在不需要将剂量增加至120 mg的患者中,达到了生化控制的85%(联合标准)。所有患者对治疗的耐受性良好。总之,Lan-Autogel可有效控制肢端肥大症患者的GH和IGF-1过度分泌,并且起效迅速。

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