Alexopoulou O, Abrams P, Verhelst J, Poppe K, Velkeniers B, Abs R, Maiter D
Department of Endocrinology, UCL-St Luc Hospital, Brussels, Belgium.
Eur J Endocrinol. 2004 Sep;151(3):317-24. doi: 10.1530/eje.0.1510317.
This open label, multicentre study was designed to evaluate the efficacy and tolerability of lanreotide Autogel (L-Autogel) in acromegalic patients over a 24-week period. The outcome of treatment with this new, long-acting, aqueous formulation of lanreotide was also compared with the patients' previous treatment with octreotide long acting repeatable (LAR).
Twenty-five acromegalic patients (13 males, mean age 51+/-12 years) were switched from octreotide LAR (20-40 mg/4 weeks for at least 6 months) to L-Autogel, given deep subcutaneously at a fixed dose of 90 mg/4 weeks. After 12 weeks, the dose of L-Autogel was titrated according to patients' mean GH and IGF-I levels at week 8. It was increased to 120 mg/4 weeks if GH>2.5 microg/l or if IGF-I was above the age-adjusted normal range. It was reduced to 60 mg/4 weeks if mean GH<1 microg/l and IGF-I was within the normal range. If the values did not fall within these ranges, the dose remained unchanged at 90 mg.
After 24 weeks of treatment with L-Autogel (final doses 60 mg in 3 patients, 90 mg in 4 patients and 120 mg in 18 patients), mean serum GH (2.9+/-2.4 microg/l) and IGF-I concentrations (332+/-193 microg/l) remained statistically unchanged when compared with baseline values under octreotide LAR (GH 2.4+/-1.8 microg/l and IGF-I 337+/-201 microg/l, non significant (NS)). There was a significant improvement of the acromegalic symptom score over the study period, from 4.8+/-3.4 to 2.8+/-2.5 (P<0.001) and a small but significant reduction in the residual pituitary tumour volume (P<0.05). Local side-effects were observed less frequently and no technical problems were encountered with the L-Autogel injections, as opposed to treatment with octreotide LAR (60 difficult injections/150 (P<0.001)).
L-Autogel appears to be as effective as octreotide LAR in lowering GH and IGF-I concentrations in acromegalic patients. This treatment was also well tolerated by the patients, giving fewer local side-effects and technical problems with injections. These advantages may improve the long-term acceptability of medical treatment in acromegaly.
本开放性、多中心研究旨在评估兰瑞肽长效凝胶(L - Autogel)在24周内对肢端肥大症患者的疗效和耐受性。还将这种新型长效水性兰瑞肽制剂的治疗结果与患者先前使用的奥曲肽长效重复注射剂(LAR)的治疗结果进行了比较。
25例肢端肥大症患者(13例男性,平均年龄51±12岁)从奥曲肽LAR(20 - 40mg/4周,至少使用6个月)转换为L - Autogel,以90mg/4周的固定剂量皮下深部注射。12周后,根据患者第8周的平均生长激素(GH)和胰岛素样生长因子 - I(IGF - I)水平对L - Autogel的剂量进行滴定。如果GH>2.5μg/l或IGF - I高于年龄校正后的正常范围,则剂量增加至120mg/4周。如果平均GH<1μg/l且IGF - I在正常范围内,则剂量减至60mg/4周。如果数值不在这些范围内,剂量保持90mg不变。
用L - Autogel治疗24周后(最终剂量:3例患者为60mg,4例患者为90mg,18例患者为120mg),与奥曲肽LAR治疗时的基线值(GH 2.4±1.8μg/l,IGF - I 337±201μg/l,无显著性差异(NS))相比,血清平均GH(2.9±2.4μg/l)和IGF - I浓度(332±193μg/l)在统计学上无变化。在研究期间,肢端肥大症症状评分有显著改善,从4.8±3.4降至2.8±2.5(P<0.001),垂体残余肿瘤体积有小幅但显著的减小(P<0.05)。与奥曲肽LAR治疗相比,L - Autogel注射引起的局部副作用观察到的频率较低,且未遇到技术问题(奥曲肽LAR治疗有60次注射困难/150次(P<0.001))。
L - Autogel在降低肢端肥大症患者的GH和IGF - I浓度方面似乎与奥曲肽LAR一样有效。该治疗方法患者耐受性良好,局部副作用较少,注射技术问题也较少。这些优点可能会提高肢端肥大症药物治疗的长期可接受性。