Rutkowski Piotr, Symonides Małgorzata, Zdzienicki Marcin, Siedlecki Janusz A
Department of Soft Tissue/Bone Sarcoma and Melanoma, M. Sklodowska-Curie Memorial Cancer Center and Institute of Oncology, Warsaw, Poland.
Recent Pat Anticancer Drug Discov. 2008 Jun;3(2):88-99. doi: 10.2174/157489208784638749.
Gastrointestinal stromal tumors (GISTs) comprise a recently defined entity of the most common mesenchymal neoplasms of the gastrointestinal tract. Advances in the understanding of the molecular mechanisms of GIST pathogenesis have resulted in the development of a treatment approach which has become a model of targeted therapy in oncology. The introduction of imatinib mesylate (inhibiting KIT/PDGFRA (platelet-derived growth factor receptor-alpha) and their downstream signaling cascade) has revolutionized the therapy of advanced (inoperable and/or metastatic) GISTs. Imatinib has now become the standard of care in the treatment of patients with advanced GIST. However, a majority of patients eventually develop clinical resistance to imatinib. Over the last few years major progress has been made in elucidating the mechanism of disease progression (as secondary mutations in KIT and/or PDGFRA kinase domains) and resistance to imatinib. Currently, the sole approved second-line drug is sunitinib--a multitargeted agent, an inhibitor of tyrosine kinase, of KIT and PDGFRA/B and of the vascular endothelial growth factor receptors (VEGFRs)-1, -2 and 3, FMS-like tyrosine kinase-3 (FLT3), colony stimulating factor 1 receptor (CSF-1R), and glial cell-line derived neurotrophic factor receptor (REarranged during Transfection; RET). However, a number of new generation tyrosine kinase inhibitors, alone or in combination, are being evaluated at present alongside treatment options alternative to inhibiting the KIT signaling pathway (as heat shock protein 90 or mammalian target of rapamycin). This article discusses the factors relating to imatinib resistance as well as upcoming potentially effective treatment options for patients with progressive disease available in 2008 and those under investigation with more individualized treatment methods, which has been recently patented. This review focuses on the current achievements in targeted therapy of advanced GISTs, and how the insight into the resistance mechanisms may allow in the near future to treat patients with advanced GISTs.
胃肠道间质瘤(GISTs)是最近定义的一种胃肠道最常见的间充质肿瘤。对GIST发病机制分子机制认识的进展导致了一种治疗方法的发展,该方法已成为肿瘤学中靶向治疗的典范。甲磺酸伊马替尼(抑制KIT/血小板衍生生长因子受体α(PDGFRA)及其下游信号级联反应)的引入彻底改变了晚期(无法手术切除和/或转移性)GIST的治疗。伊马替尼现已成为晚期GIST患者治疗的标准疗法。然而,大多数患者最终会对伊马替尼产生临床耐药性。在过去几年中,在阐明疾病进展机制(如KIT和/或PDGFRA激酶结构域中的二次突变)和对伊马替尼的耐药性方面取得了重大进展。目前,唯一获批的二线药物是舒尼替尼——一种多靶点药物,是酪氨酸激酶、KIT和PDGFRA/B以及血管内皮生长因子受体(VEGFRs)-1、-2和-3、FMS样酪氨酸激酶-3(FLT3)、集落刺激因子1受体(CSF-1R)和胶质细胞系衍生神经营养因子受体(转染过程中重排;RET)的抑制剂。然而,目前正在评估许多新一代酪氨酸激酶抑制剂单独或联合使用的情况,以及替代抑制KIT信号通路的治疗选择(如热休克蛋白90或雷帕霉素的哺乳动物靶点)。本文讨论了与伊马替尼耐药相关的因素,以及2008年可用于进展性疾病患者的即将出现的潜在有效治疗选择,以及正在研究的更个体化治疗方法,这些方法最近已获得专利。本综述重点关注晚期GIST靶向治疗的当前成就,以及对耐药机制的深入了解如何在不久的将来用于治疗晚期GIST患者。