Ma Pei, Huang Ruohan, Gu Yunru, Fang Yuan, Wu Xi, Chen Dong-Sheng, Zhang Han-Wu, Gao Wen, Shu Yongqian
Department of Oncology, The First Affiliated Hospital of Nanjing Medical University.
Jiangsu Simcere Diagnostics Co., Ltd, The State Key Laboratory of Translational Medicine and Innovative Drug Development, Nanjing, China.
Anticancer Drugs. 2022 Nov 1;33(10):1186-1190. doi: 10.1097/CAD.0000000000001370. Epub 2022 Aug 10.
Epidermal growth factor receptor-tyrosine kinase inhibitors (EGFR-TKIs) have significantly improved response in all stages of patients with EGFR positive mutations in nonsmall cell lung cancer. However, the primary resistance mechanism of EGFR-TKIs has not been thoroughly revealed. Here, we described a case of a 64-year-old male with lung adenocarcinoma presented primary resistance on osimertinib combined with bevacizumab and platinum-based chemotherapy, next-generation sequencing revealed EGFR exon 21 L858R mutation and MET gene amplification. Afterward, savolitinib monotherapy was started until now, and the treatment was temporarily successful, the last follow-up clinical evaluation was near complete response, the progression-free survival has over 7 months. Our case highlights that EGFR-TKIs may be not the optimal choice for lung adenocarcinoma with primary EGFR -sensitive mutation with MET amplification simultaneously, whereas MET inhibitor alone may be an effective treatment option. In clinical practice, we should fully consider the possibility of primary resistance in EGFR-TKIs administration.
表皮生长因子受体酪氨酸激酶抑制剂(EGFR-TKIs)显著改善了非小细胞肺癌中EGFR阳性突变患者各阶段的反应。然而,EGFR-TKIs的主要耐药机制尚未完全阐明。在此,我们描述了一例64岁男性肺腺癌患者,对奥希替尼联合贝伐单抗及铂类化疗出现原发性耐药,二代测序显示EGFR外显子21 L858R突变及MET基因扩增。此后,开始使用赛沃替尼单药治疗至今,治疗暂时成功,最后一次随访临床评估接近完全缓解,无进展生存期已超过7个月。我们的病例强调,对于同时存在原发性EGFR敏感突变及MET扩增的肺腺癌患者,EGFR-TKIs可能并非最佳选择,而单独使用MET抑制剂可能是一种有效的治疗选择。在临床实践中,我们应充分考虑EGFR-TKIs给药时原发性耐药的可能性。