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首页> 外文期刊>Experimental and clinical endocrinology and diabetes: Official journal, German Society of Endocrinology [and] German Diabetes Association >Four-year follow-up of acromegalic patients treated with the new long-acting formulation of lanreotide (lanreotide autogel).
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Four-year follow-up of acromegalic patients treated with the new long-acting formulation of lanreotide (lanreotide autogel).

机译:使用新的长效制剂兰瑞肽(lanreotide autogel)治疗肢端肥大症患者,为期四年。

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Lanreotide Autogel (Ipsen) is a long-acting somatostatin analogue (SA) in a new galenic formulation suitable for subcutaneous (s.c.) injection. In our department, 11 patients with therapy-resistant acromegaly were treated with Lanreotide Autogel for 48 months. 10/11 patients had previously undergone transsphenoidal surgery. For a median duration of 1.4 years prior to Lanreotide Autogel, the patients received Lanreotide PR 30 mg every 7, 10, or 14 days. 60, 90, or 120 mg of Lanreotide Autogel was administered by deep s.c. injection every 28 days, with the higher dosage being given to those with the previously shortest injection interval under Lanreotide PR. Dose was adjusted on the basis of Growth Hormone (GH) level after 4, 8, and 12 months with a minimum dose of 60 mg and a maximum dose of 120 mg. The efficacy of Lanreotide Autogel treatment was evaluated by measuring GH concentrations (4 hour profiles) and IGF-I levels. Before switching to Lanreotide Autogel, the multiple of the upper limit of normal(xULN) of IGF-I levels was 1.2 (median) and the median GH level was 1.3 microg/l. 3 out of 11 patients had an IGF-I within the age- and sex-adjusted normal range. After 48 months of treatment with Lanreotide Autogel, six patients had an IGF-I within the normal range. Median GH levels were at 1.3 microg/l and xULN of IGF-I was at 1.0 compared to Lanreotide PR 30 mg treatment (p < 0.001). At the end of the study, 8 patients received 120 mg Lanreotide Autogel, 2 patients 90 mg and 1 patient 60 mg, respectively. There was slight but significant deterioration of glucose metabolism with an increase of HbA1c. In conclusion, the new galenic formulation of Lanreotide improves not only the control of biochemical markers of acromegaly compared to the conventional PR formulation, but is also easier to administer given its deep s.c. method of administration. Glucose metabolism has to be followed carefully in patients on high-dose Lanreotide Autogel.
机译:Lanreotide Autogel(Ipsen)是一种长效生长抑素类似物(SA),是一种适用于皮下(s.c.)注射的新型盖仑制剂。在我们的科室中,使用兰瑞肽Autogel治疗了11例具有治疗耐药性的肢端肥大症患者48个月。 10/11例患者以前接受过蝶窦手术。在使用Lanreotide Autogel之前,中位时间为1.4年,患者每7、10或14天接受Lanreotide PR 30 mg。 60、90或120 mg Lanreotide Autogel通过深层皮下注射。每隔28天注射一次,根据Lanreotide PR的规定,以前间隔最短的患者应给予较高剂量。在4、8和12个月后,根据生长激素(GH)的水平调整剂量,最小剂量为60 mg,最大剂量为120 mg。兰瑞肽Autogel治疗的疗效通过测量GH浓度(4小时)和IGF-I水平进行评估。改用兰瑞肽Autogel之前,IGF-I正常水平上限(xULN)的倍数为1.2(中值),中位GH水平为1.3 microg / l。 11名患者中有3名的IGF-I在年龄和性别调整后的正常范围内。用兰瑞肽Autogel治疗48个月后,有6名患者的IGF-I在正常范围内。与兰瑞肽PR 30毫克治疗相比,中位GH水平为1.3微克/升,xULN的IGF-I为1.0(p <0.001)。在研究结束时,分别有8位患者接受120 mg兰瑞肽Autogel,2位患者90 mg和1位患者60 mg。随着HbA1c的增加,葡萄糖代谢有轻微但明显的恶化。总之,与常规的PR制剂相比,新的兰瑞肽的盖伦制剂不仅改善了肢端肥大症的生化标志物的控制,而且由于其深层的特性,更易于管理。管理方法。使用大剂量兰瑞肽Autogel的患者必须仔细追踪葡萄糖代谢。

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