Simmons Comprehensive Cancer Center, The University of Texas Southwestern Medical Center, Dallas, TX, United States of America; Department of Clinical Medicine and Surgery, University of Naples Federico II, Naples, Italy.
Department of Clinical Medicine and Surgery, University of Naples Federico II, Naples, Italy.
Biochim Biophys Acta Rev Cancer. 2021 Dec;1876(2):188595. doi: 10.1016/j.bbcan.2021.188595. Epub 2021 Jul 23.
Fibroblast growth factors (FGFs) and their receptors (FGFRs) have been extensively investigated in solid malignancies, representing an attractive therapeutic target. In breast cancer, especially in estrogen receptor positive (ER+) subtype, FGFR signaling aberrations have been reported to contribute to proliferation, dedifferentiation, metastasis and drug resistance. However, clinical trials evaluating the use of FGFR inhibitors in breast cancer have had disappointing results. The different biological properties of distinct FGFR alterations and lack of established patient selection criteria, in addition to the early use of non-selective inhibitors, are possible reasons of this failure. Herein, we review the current knowledge regarding the role of FGFR signaling in endocrine resistance in breast cancer. We will also summarize the results from the clinical development of FGFR inhibitors in breast cancer, discussing future challenges to identify the correct cohorts of patients to enroll in trials testing FGFR inhibitors.
成纤维细胞生长因子(FGFs)及其受体(FGFRs)在实体恶性肿瘤中得到了广泛研究,是一个有吸引力的治疗靶点。在乳腺癌中,特别是在雌激素受体阳性(ER+)亚型中,FGFR 信号异常被报道有助于增殖、去分化、转移和耐药。然而,评估 FGFR 抑制剂在乳腺癌中应用的临床试验结果令人失望。不同 FGFR 改变的生物学特性、缺乏既定的患者选择标准,以及早期使用非选择性抑制剂,都可能是导致这一失败的原因。在此,我们综述了 FGFR 信号在内分泌耐药性乳腺癌中的作用的最新知识。我们还将总结 FGFR 抑制剂在乳腺癌临床开发中的结果,讨论未来的挑战,以确定正确的患者队列,纳入试验测试 FGFR 抑制剂。