Mangano Alberto, Lianos Georgios D, Roukos Dimitrios H, Mason Sam E, Kim Hoon Yub, Dionigi Gianlorenzo
First Department of General Surgery Ospedale di Circolo e Fondazione Macchi Varese, Department of Human Morphology & Surgical Sciences Insubria University Varese-Como, Italy.
Department of General Surgery Ioannina University Hospital, Centre for Biosystems & Genomic Network Medicine Ioannina University, Ioannina, Greece.
Future Oncol. 2016;12(8):1059-65. doi: 10.2217/fon.16.8. Epub 2016 Feb 26.
Neuroendocrine tumors (NETs) are rare and heterogeneous tumors and there is a paucity of randomized clinical trials evaluating the different therapeutic strategies. Over recent years, some important molecular aspects have been investigated and multiple targeted therapies are currently available. One of the most promising targets for the therapy of NETs are the mTOR and angiogenic growth factor receptors. The advent of the inhibitors of the mTOR pathway, tyrosine kinase inhibitors and of somatostatin analogs have shown their efficacy in randomized clinical trials in terms of implementing clinical hormone-induced syndromes and progression-free survival of advanced NETs. This article summarizes the standard therapies and new perspectives in NET's treatment, which remains still very heterogeneous and little known entity.
神经内分泌肿瘤(NETs)是罕见的异质性肿瘤,评估不同治疗策略的随机临床试验较少。近年来,一些重要的分子方面已得到研究,目前有多种靶向治疗方法。治疗NETs最有前景的靶点之一是mTOR和血管生成生长因子受体。mTOR通路抑制剂、酪氨酸激酶抑制剂和生长抑素类似物的出现已在随机临床试验中显示出它们在改善晚期NETs的临床激素诱导综合征和无进展生存期方面的疗效。本文总结了NETs治疗中的标准疗法和新观点,NETs仍是一个非常异质性且鲜为人知的实体。