Columbia University College of Physicians and Surgeons, St. Luke's-Roosevelt Hospital Center, Department of Medicine, New York, USA.
Expert Opin Pharmacother. 2013 Apr;14(6):783-92. doi: 10.1517/14656566.2013.776540. Epub 2013 Mar 4.
Sunitinib , a broad-spectrum multikinase inhibitor, was recently approved for use in progressive, well-differentiated pancreatic neuroendocrine tumors (pNETs). Its mechanism of action affects various signaling cascades involving antiangiogenesis and tumor proliferation, including vascular endothelial growth factors and platelet-derived growth factors.
In this article, we review sunitinib's mechanism of action at a molecular level and review key preclinical and clinical studies for pNETs and more limited data regarding sunitinib's evaluation in pancreas adenocarcinoma. The data for sunitinib in pNETs are placed in the context of the changing landscape of therapeutic options for this cancer, and relevant ongoing clinical trials and future directions are highlighted.
Sunitinib malate has become integrated into routine clinical management for pNETs; however, its role in pancreas adenocarcinoma is not established.
舒尼替尼是一种广谱多激酶抑制剂,最近被批准用于治疗进展期、分化良好的胰腺神经内分泌肿瘤(pNET)。其作用机制影响包括血管内皮生长因子和血小板衍生生长因子在内的多种参与抗血管生成和肿瘤增殖的信号级联。
本文从分子水平上综述了舒尼替尼的作用机制,并回顾了用于 pNET 的关键临床前和临床研究,以及关于舒尼替尼在胰腺腺癌中的评估的更有限的数据。将 pNET 中舒尼替尼的数据置于癌症治疗选择不断变化的背景下,并强调了相关的正在进行的临床试验和未来方向。
苹果酸舒尼替尼已纳入 pNET 的常规临床管理;然而,其在胰腺腺癌中的作用尚未确定。