首页> 外文期刊>Annals of oncology: official journal of the European Society for Medical Oncology >The clinical management of neuroendocrine tumors with long-acting repeatable (LAR) octreotide: comparison with standard subcutaneous octreotide therapy.
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The clinical management of neuroendocrine tumors with long-acting repeatable (LAR) octreotide: comparison with standard subcutaneous octreotide therapy.

机译:长效可重复(LAR)奥曲肽对神经内分泌肿瘤的临床治疗:与标准皮下奥曲肽治疗的比较。

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摘要

Neuroendocrine tumors are rare, occurring in less than 1% of the population. They are divided clinically into functionally active or non-active tumors. Functionally active tumors produce a variety of substances (mainly peptides or serotonin) that are responsible for symptoms and sometimes can lead to the death of the patient independently from tumor proliferation. The most important compounds that can control symptoms in these patients are somatostatin analogs. Native somatostatin is not suitable for long-term clinical application due to its short half-life. Therefore, synthetic drugs were developed with improved pharmacokinetic characteristics. The best-characterized analog, octreotide, has been successfully applied to patients with functioning tumors. Octreotide can ameliorate symptoms in 30%-70% of the patients, mainly through a direct inhibitory effect on hormone production from the tumors. There is little or no effect on tumor growth during octreotide therapy; clinical responses were recorded in only 10%-30% of the patients. Recently, significant improvement in the management of the disease has been demonstrated with long-acting repeatable (LAR) octreotide. This new formulation requires only one monthly intramuscolar injection, and shows better acceptability and patient compliance to therapy. Data available to date show superimposable results of both standard octreotide and LAR octreotide in controlling symptoms, lowering hormone and tumor marker levels, and in reducing tumor growth. The availability of long-acting molecules have permitted the exploration of high-dose therapy in increasing tumor shrinkage and prolonging survival. Although there is a clear dose-response trend, the published data are not conclusive and further investigations are needed. The possible lack of cross-resistance between LAR octreotide and a different analog, Lanreotide, is a very stimulating finding and this might lead to the development of new therapeutical strategies in the management of neuroendocrine tumors.
机译:神经内分泌肿瘤很少见,仅占不到1%的人口。它们在临床上分为功能性活动性或非活动性肿瘤。具有功能活性的肿瘤产生多种物质(主要是肽或5-羟色胺),这些物质负责症状,有时可能独立于肿瘤扩散而导致患者死亡。可以控制这些患者症状的最重要化合物是生长抑素类似物。天然生长抑素半衰期短,不适合长期临床应用。因此,开发了具有改善的药代动力学特性的合成药物。表征最好的类似物奥曲肽已成功应用于患有功能性肿瘤的患者。奥曲肽可以改善30%-70%的患者症状,主要是通过直接抑制肿瘤中激素的产生。奥曲肽治疗期间对肿瘤的生长几乎没有影响。仅10%-30%的患者记录了临床反应。最近,长效可重复(LAR)奥曲肽已证明该疾病的治疗有显着改善。这种新配方仅需每月一次肌内注射,显示出更好的可接受性和患者对治疗的依从性。迄今为止可获得的数据显示标准奥曲肽和LAR奥曲肽在控制症状,降低激素和肿瘤标志物水平以及减少肿瘤生长方面均具有叠加效果。长效分子的可用性已允许探索高剂量疗法,以增加肿瘤缩小和延长生存期。尽管存在明显的剂量反应趋势,但公开的数据尚无定论,需要进一步研究。 LAR奥曲肽与另一种类似物Lanreotide之间可能缺乏交叉耐药性,这是一个非常令人振奋的发现,这可能会导致神经内分泌肿瘤治疗新疗法的发展。

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