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肢端肥大症的药物治疗:生长抑素类似物的疗效与安全性

Medical therapy of acromegaly: efficacy and safety of somatostatin analogues.

作者信息

Feelders Richard A, Hofland Leo J, van Aken Maarten O, Neggers Sebastian J, Lamberts Steven W J, de Herder Wouter W, van der Lely Aart-Jan

机构信息

Department of Internal Medicine, Section of Endocrinology, Erasmus Medical Center, Rotterdam, The Netherlands.

出版信息

Drugs. 2009 Nov 12;69(16):2207-26. doi: 10.2165/11318510-000000000-00000.

Abstract

Acromegaly is a chronic disease with signs and symptoms due to growth hormone (GH) excess. The most frequent cause of acromegaly is a GH-producing pituitary adenoma. Chronic GH excess is accompanied by long-term complications of the locomotor (arthrosis) and cardiovascular (atherosclerosis, cardiomyopathy) systems and is, when untreated, associated with an increased mortality. The aim of treatment of acromegaly is to improve symptoms, to achieve local tumour mass control, and to decrease morbidity and mortality. Treatment options include surgery, medical therapy and radiotherapy. Transsphenoidal surgery is the first choice of treatment when a definitive cure can be achieved, particularly in the case of microadenomas and when decompression of surrounding structures (optic chiasm, ophthalmic motor nerves) is indicated. Primary medical therapy has been increasingly applied in recent years, especially when a priori chances of surgical cure are low (because of adenoma size and localization) and in patients with advanced age and/or serious co-morbidity. In addition, preoperative primary medical therapy may result in tumour shrinkage, facilitating tumour resection, and may reduce perioperative complications due to GH excess. Within the spectrum of medical therapy, long-acting somatostatin analogues (somatostatins) are considered as first-line treatment. Treatment with somatostatin analogues results in GH control in approximately 60% of patients. In addition, somatostatin analogues induce tumour shrinkage in 30-50% of patients, particularly when applied as primary therapy. Prolonged treatment with somatostatin analogues appears to be safe and is usually well tolerated. The currently available somatostatin analogues, octreotide and lanreotide, seem to be equally effective; however, this should still be evaluated in prospective, randomized trials evaluating efficacy with respect to GH control and tumour shrinkage. In patients with an insufficient clinical and biochemical response to somatostatin analogues, combination therapy with dopamine receptor agonists or the GH receptor antagonist pegvisomant usually leads to disease control. New developments in the medical therapy of acromegaly include the universal somatostatin receptor agonist pasireotide, which has a broader affinity for all somatostatin receptor (sst) subtypes compared with the currently available somatostatin analogues with preferential affinity for the sst2 receptor, and chimeric compounds that interact with both somatostatin and dopamine receptors with synergizing effects on GH secretion.

摘要

肢端肥大症是一种由于生长激素(GH)分泌过多而出现相应体征和症状的慢性疾病。肢端肥大症最常见的病因是分泌GH的垂体腺瘤。长期GH分泌过多会伴有运动系统(关节病)和心血管系统(动脉粥样硬化、心肌病)的长期并发症,若不治疗,会增加死亡率。肢端肥大症的治疗目标是改善症状、实现局部肿瘤肿块控制并降低发病率和死亡率。治疗选择包括手术、药物治疗和放射治疗。当能够实现根治时,经蝶窦手术是首选治疗方法,特别是对于微腺瘤以及需要对周围结构(视交叉、眼运动神经)进行减压的情况。近年来,初始药物治疗的应用越来越多,尤其是在手术治愈的先验可能性较低(由于腺瘤大小和位置)以及老年和/或有严重合并症的患者中。此外,术前初始药物治疗可能会导致肿瘤缩小,便于肿瘤切除,并可能减少因GH分泌过多引起的围手术期并发症。在药物治疗范围内,长效生长抑素类似物(生长抑素)被视为一线治疗药物。使用生长抑素类似物治疗可使约60%的患者的GH得到控制。此外,生长抑素类似物可使30%至50%的患者肿瘤缩小,尤其是在作为初始治疗应用时。长期使用生长抑素类似物似乎是安全的,且通常耐受性良好。目前可用的生长抑素类似物奥曲肽和兰瑞肽似乎同样有效;然而,这仍应在前瞻性随机试验中进行评估,该试验评估在控制GH和肿瘤缩小方面的疗效。对于对生长抑素类似物临床和生化反应不足的患者,联合使用多巴胺受体激动剂或GH受体拮抗剂培维索孟通常可实现疾病控制。肢端肥大症药物治疗的新进展包括通用生长抑素受体激动剂帕瑞肽,与目前对sst2受体具有优先亲和力的生长抑素类似物相比,它对所有生长抑素受体(sst)亚型具有更广泛的亲和力,以及与生长抑素和多巴胺受体相互作用并对GH分泌具有协同作用的嵌合化合物。

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