Christensen J G
Pfizer Global Research and Development, 10724 Science Center Drive, San Diego, CA 92121, USA.
Ann Oncol. 2007 Sep;18 Suppl 10:x3-10. doi: 10.1093/annonc/mdm408.
Sunitinib malate is an oral, multitargeted tyrosine kinase inhibitor that targets both angiogenic pathways (i.e., vascular endothelial growth factor receptor and platelet-derived growth factor receptor) and direct pro-oncogenic pathways (e.g., stem-cell factor receptor and FMS-like tyrosine kinase-3). Preclinical studies with this agent have indicated that it exhibits robust inhibitory activity against these targets. Clinical trial results have demonstrated the therapeutic potential of this agent and have implicated sunitinib targets in the pathophysiology of malignancies such as renal cell carcinoma and gastrointestinal stromal tumour. This paper reviews the preclinical data supporting the development of this agent and its translation from benchtop to bedside. It also highlights the importance of the multiple pathways that may be involved in cancer progression and the importance of these pathways in selected malignancies.
苹果酸舒尼替尼是一种口服的多靶点酪氨酸激酶抑制剂,可作用于血管生成途径(即血管内皮生长因子受体和血小板衍生生长因子受体)以及直接的促癌途径(如干细胞因子受体和FMS样酪氨酸激酶-3)。对该药物的临床前研究表明,它对这些靶点具有强大的抑制活性。临床试验结果已证明该药物的治疗潜力,并表明舒尼替尼的靶点参与了肾细胞癌和胃肠道间质瘤等恶性肿瘤的病理生理过程。本文回顾了支持该药物研发及其从实验室到临床转化的临床前数据。它还强调了可能参与癌症进展的多种途径的重要性以及这些途径在特定恶性肿瘤中的重要性。