Eisenberg Burton L
Department of Surgical Oncology, Fox Chase Cancer Center, Temple University, School of Medicine, Philadelphia, Pennsylvania, USA.
Oncology (Williston Park). 2003 Nov;17(11):1615-20; discussion 1620, 1623, 1626 passim.
Although their overall incidence is uncommon, gastrointestinal stromal tumors (GIST) are the most frequently encountered mesenchymal tumors of the GI tract. Their pathology has been recently defined by the presence of KIT (transmembrane receptor tyrosine kinase). The majority of GISTs have c-kit gain-of-function mutations mainly in exon 11 (highly conserved juxtamembrane region) that eventuates in constitutive activation of KIT, promoting proliferation and antiapoptotic signaling. Imatinib mesylate (Gleevec) is a specific inhibitor of KIT kinase activation, and in phase II clinical trials has proven to be remarkably efficacious in heavily pretreated GIST patients with advanced disease. The molecular and genomic determinants of response/resistance patterns are the subject of ongoing studies, and adjuvant studies are also under way. The initial evaluations of imatinib provide proof of concept for the hypothesis-driven design of selective molecularly targeted therapies for solid tumor malignancies.
尽管胃肠道间质瘤(GIST)的总体发病率并不常见,但却是胃肠道最常遇到的间叶性肿瘤。其病理最近已通过KIT(跨膜受体酪氨酸激酶)的存在得以明确。大多数GIST具有c-kit功能获得性突变,主要发生在外显子11(高度保守的近膜区域),这导致KIT的组成性激活,促进增殖和抗凋亡信号传导。甲磺酸伊马替尼(格列卫)是KIT激酶激活的特异性抑制剂,在II期临床试验中已证明对晚期疾病且经过大量预处理的GIST患者具有显著疗效。反应/耐药模式的分子和基因组决定因素是正在进行的研究课题,辅助研究也在进行中。伊马替尼的初步评估为实体瘤恶性肿瘤的选择性分子靶向治疗的假设驱动设计提供了概念验证。