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生长抑素类似物在胃肠胰神经内分泌肿瘤中的抗增殖作用。

Antiproliferative effect of somatostatin analogs in gastroenteropancreatic neuroendocrine tumors.

出版信息

World J Gastroenterol. 2010 Jun 28;16(24):2963-70. doi: 10.3748/wjg.v16.i24.2963.

Abstract

Somatostatin analogs were initially developed for the control of hormonal syndromes associated with neuroendocrine tumors (NETs). In recent years, accumulating data has supported their role as antiproliferative agents, capable of stabilizing tumor growth in patients with metastatic neuroendocrine malignancies, including carcinoid and pancreatic endocrine tumors. A phase III, randomized, placebo-controlled trial has now demonstrated that octreotide long-acting repeatable (LAR) 30 mg can significantly prolong time to tumor progression among patients with metastatic midgut NETs regardless of functional status, chromogranin A level or age. In addition to significantly lengthening time to tumor progression in the overall study population, subset analysis suggests that patients with low tumor burden are most likely to experience disease stabilization with octreotide LAR 30 mg, supporting the early use of octreotide LAR in patients with metastatic disease. Further research efforts are underway to evaluate the use of somatostatin analogs as antiproliferative agents in other types of gastroenteropancreatic-NETs. Ongoing studies are also evaluating novel somatostatin analogs and somatostatin analogs in combination with other anti-tumor therapies.

摘要

生长抑素类似物最初是为了控制与神经内分泌肿瘤(NET)相关的激素综合征而开发的。近年来,越来越多的数据支持其作为抗增殖剂的作用,能够稳定转移性神经内分泌恶性肿瘤患者的肿瘤生长,包括类癌和胰腺内分泌肿瘤。一项 III 期、随机、安慰剂对照试验现已表明,奥曲肽长效重复(LAR)30mg 可显著延长转移性中肠 NET 患者的无进展生存期,无论其功能状态、嗜铬粒蛋白 A 水平或年龄如何。除了在整个研究人群中显著延长肿瘤进展时间外,亚组分析表明,肿瘤负担较低的患者最有可能因奥曲肽 LAR 30mg 而稳定疾病,这支持在转移性疾病患者中尽早使用奥曲肽 LAR。目前正在进行进一步的研究,以评估生长抑素类似物作为其他类型的胃肠胰神经内分泌肿瘤的抗增殖剂的用途。正在进行的研究还评估了新型生长抑素类似物和生长抑素类似物联合其他抗肿瘤疗法的疗效。

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