a Department of Molecular and Translational Medicine , University of Brescia , Brescia , Italy.
Expert Rev Anticancer Ther. 2018 Sep;18(9):861-872. doi: 10.1080/14737140.2018.1491795. Epub 2018 Jul 2.
Deregulation of the fibroblast growth factor (FGF)/FGF receptor (FGFR) network occurs frequently in tumors due to gene amplification, activating mutations, and oncogenic fusions. Thus, the development of FGF/FGFR-targeting therapies is the focus of several basic, preclinical, and clinical studies. Areas covered: This review will recapitulate the status of current FGF/FGFR-targeted drugs. Expert commentary: Non-selective FGF/FGFR inhibitors have been approved for cancer treatment but evidence highlights various complications affecting their use in the clinical practice. It appears mandatory to identify FGF/FGFR alterations and appropriate biomarkers that may predict and monitor response to treatment, to establish the contribution of the FGF/FGFR system to the onset of mechanisms of drug resistance, and to develop effective combinations of FGF/FGFR inhibitors with other targeted therapies.
由于基因扩增、激活突变和致癌融合,成纤维细胞生长因子 (FGF)/成纤维细胞生长因子受体 (FGFR) 网络的失调在肿瘤中经常发生。因此,FGF/FGFR 靶向治疗的发展是几项基础、临床前和临床研究的重点。
本综述将概述当前 FGF/FGFR 靶向药物的状况。
非选择性 FGF/FGFR 抑制剂已被批准用于癌症治疗,但有证据表明,各种并发症会影响其在临床实践中的应用。似乎必须确定 FGF/FGFR 的改变和适当的生物标志物,这些改变和生物标志物可能预测和监测对治疗的反应,以确定 FGF/FGFR 系统对耐药机制发生的贡献,并开发 FGF/FGFR 抑制剂与其他靶向治疗的有效组合。