Brazel Danielle, Nagasaka Misako
Department of Medicine, University of California Irvine School of Medicine, Orange, CA, USA.
Chao Family Comprehensive Cancer Center, Orange, CA, USA.
Lung Cancer (Auckl). 2021 Dec 2;12:133-138. doi: 10.2147/LCTT.S337861. eCollection 2021.
Non-small cell lung cancer (NSCLC) patients demonstrating sensitizing oncogenic driver mutations have derived clinical benefit from targeted therapy. EGFR mutations constitutively activate the signaling pathway, leading to prosurvival and antiapoptotic signals. Classic sensitizing EGFR mutations, such as exon 19 deletions and exon 21 L858R point mutations, respond well to tyrosine kinase inhibitors (TKIs). On the other hand, EGFR exon 20 in-frame insertions are observed in 4-12% of EGFR-mutated NSCLC and are resistant to targeted therapy with TKIs. In May 2021, the Federal Drug Administration (FDA) provided accelerated approval to amivantamab (Rybrevant) in adults with locally advanced or metastatic NSCLC with EGFR exon 20 insertion mutations after treatment with platinum-based chemotherapy. Here, we discuss properties of amivantamab, clinical trial results, and management of patients with EGFR exon 20 insertion mutated NSCLC.
表现出敏感致癌驱动基因突变的非小细胞肺癌(NSCLC)患者已从靶向治疗中获得临床益处。EGFR突变可组成性激活信号通路,导致促生存和抗凋亡信号。经典的敏感EGFR突变,如19外显子缺失和21外显子L858R点突变,对酪氨酸激酶抑制剂(TKIs)反应良好。另一方面,在4%-12%的EGFR突变NSCLC中观察到EGFR 20外显子框内插入,且对TKIs靶向治疗耐药。2021年5月,美国食品药品监督管理局(FDA)加速批准了amivantamab(Rybrevant)用于治疗接受铂类化疗后出现EGFR 20外显子插入突变的局部晚期或转移性NSCLC成人患者。在此,我们讨论amivantamab的特性、临床试验结果以及EGFR 20外显子插入突变NSCLC患者的管理。