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[用长效兰瑞肽治疗肢端肥大症。一种新的生长抑素类似物]

[Treatment of acromegaly with sustained-release lanreotide. A new somatostatin analog].

作者信息

Heron I, Thomas F, Dero M, Poutrain J R, Henane S, Catus F, Kuhn J M

机构信息

Service d'Endocrinologie, CHU de Rouen.

出版信息

Presse Med. 1993 Mar 27;22(11):526-31.

PMID:8099735
Abstract

The recovery of acromegaly is not obtained in about 50 percent of cases treated with radiotherapy and/or transsphenoidal surgery. Somatostatin analogs prescribed in such cases are effective but need either several subcutaneous injections a day or continuous infusions with pumps. Long-acting formulations of the new somatostatin analog lanreotide should avoid such drawbacks. Nine acromegalics, not cured by pituitary surgery (associated with radiotherapy in 7) received on IM injection of a long acting formulation of lanreotide twice a month for one year. Basal evaluation included: clinical examination, routine analyses, gall bladder ultrasonography, hormonal investigation of pituitary function including GH and IgF-1 measurements, visual field evaluation and pituitary scanning. A similar evaluation was performed on months 6 and 12 of treatment. The clinical symptoms of acromegaly progressively improved during therapy. Plasma GH levels decreased significantly (P < 0.01) from 24.2 +/- 2.1 to 9.3 +/- 1.2, 6.4 +/- 1.4 and 7.9 +/- 1.1 micrograms/l on months 3, 6 and 12, respectively. Plasma IgF-1 levels were normalized, decreasing from 676 +/- 40 to 331 +/- 30, 350 +/- 36, and 317 +/- 29 ng/ml on months 3, 6 and 12, respectively. Plasma lanreotide levels remained stable throughout the treatment. Side-effects included slight and transient diarrhoea and abdominal cramps which disappeared after 6 months of treatment. No gallstones appeared during treatment. These results show that one injection, twice a month, of a long-acting formulation containing 30 mg lanreotide is able to control the evolutivity of acromegalies not cured by pituitary radiotherapy and/or transsphenoidal surgery. Such formulations are well tolerated and avoid the drawbacks of either several subcutaneous injections a day or continuous infusions of somatostatin analogs.

摘要

在接受放射治疗和/或经蝶窦手术的病例中,约50%无法实现肢端肥大症的康复。在此类病例中开具的生长抑素类似物有效,但需要每天进行几次皮下注射或使用泵持续输注。新型生长抑素类似物兰瑞肽的长效制剂应可避免这些缺点。9例肢端肥大症患者,垂体手术未能治愈(7例联合放射治疗),每月接受1次30mg兰瑞肽长效制剂的肌肉注射,持续1年。基础评估包括:临床检查、常规分析、胆囊超声检查、垂体功能的激素检查,包括生长激素(GH)和胰岛素样生长因子-1(IgF-1)测量、视野评估和垂体扫描。在治疗的第6个月和第12个月进行了类似评估。在治疗期间,肢端肥大症的临床症状逐渐改善。血浆生长激素水平显著下降(P<0.01),在第3、6和12个月时分别从24.2±2.1降至9.3±1.2、6.4±1.4和7.9±1.1μg/L。血浆胰岛素样生长因子-1水平恢复正常,在第3、6和12个月时分别从676±40降至331±30、350±36和317±29ng/ml。在整个治疗过程中,血浆兰瑞肽水平保持稳定。副作用包括轻微且短暂的腹泻和腹部绞痛,在治疗6个月后消失。治疗期间未出现胆结石。这些结果表明,每月注射1次含30mg兰瑞肽的长效制剂能够控制垂体放射治疗和/或经蝶窦手术未能治愈的肢端肥大症的病情发展。此类制剂耐受性良好,避免了每天多次皮下注射或生长抑素类似物持续输注的缺点。

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