O'Neal Comprehensive Cancer Center, Department of Radiation Oncology, The University of Alabama at Birmingham Heersink School of Medicine, Birmingham, AL 35233, USA.
Int J Mol Sci. 2022 Mar 30;23(7):3818. doi: 10.3390/ijms23073818.
EGFR is a prototypical receptor tyrosine kinase that is overexpressed in multiple cancers including head and neck squamous cell carcinoma (HNSCC). The standard of care for HNSCC remains largely unchanged despite decades of research. While EGFR blockade is an attractive target in HNSCC patients and anti-EGFR strategies including monoclonal antibodies and kinase inhibitors have shown some clinical benefit, efficacy is often due to the eventual development of resistance. In this review, we discuss how the acquisition of mutations in various domains of the EGFR gene not only alter drug binding dynamics giving rise to resistance, but also how mutations can impact radiation response and overall survival in HNSCC patients. A better understanding of the EGFR mutational landscape and its dynamic effects on treatment resistance hold the potential to better stratify patients for targeted therapies in order to maximize therapeutic benefits.
表皮生长因子受体(EGFR)是一种典型的受体酪氨酸激酶,在多种癌症中过度表达,包括头颈部鳞状细胞癌(HNSCC)。尽管经过几十年的研究,HNSCC 的标准治疗方法仍然基本没有改变。尽管 EGFR 阻断在 HNSCC 患者中是一个有吸引力的靶点,并且包括单克隆抗体和激酶抑制剂在内的抗 EGFR 策略已经显示出一些临床获益,但疗效往往归因于最终产生的耐药性。在这篇综述中,我们讨论了 EGFR 基因的各个域中获得的突变不仅如何改变药物结合动力学从而导致耐药性,还讨论了突变如何影响 HNSCC 患者的放射反应和总生存。更好地了解 EGFR 突变景观及其对治疗耐药性的动态影响,有可能更好地对患者进行靶向治疗分层,以最大限度地提高治疗效益。