Non-small cell lung cancer with MET exon 14 skipping alteration responding to immunotherapy: a case report

被引:2
作者
Chen, Zhuxing
Zhu, Feng
Li, Caichen
Li, Jianfu
Cheng, Bo
Xiong, Shan
Zhong, Ran
Liang, Wenhua [1 ]
He, Jianxing [1 ]
机构
[1] Guangzhou Med Univ, Affiliated Hosp 1, Dept Thorac Surg Oncol, State Key Lab, 151 Yanjiang West Rd, Guangzhou, Peoples R China
关键词
Non-small cell lung cancer (NSCLC); MET exon 14 skipping alteration; immunotherapy; programmed cell death protein 1; cytotoxic t-lymphocyte associated protein 4 (CTLA-4);
D O I
10.21037/atm-20-6829
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Immunotherapy has been proved to be a promising candidate for advanced non-small cell lung cancer (NSCLC). Despite MET mutations are regarded as an independent factor of programmed death ligand 1 (PD-L1) high expression, the efficacy of immune checkpoint inhibitors (ICIs) across NSCLC harboring Mesenchymal-epithelial transition factor exon 14 skipping alteration (METex14) is still uncleared. Moreover, when the resistance of PD-1 antibody occurs, the questions of how to interpret the resistance and how to overcome the resistance are worth exploring. We report a case of NSCLC with METex14 developed a right femoral metastasis after responding well to neoadjuvant immunotherapy, a successful lobectomy, and adjuvant immunotherapy. The subsequent attempts of MET targeted inhibitor, concurrent chemoradiotherapy, and notably programmed cell death protein 1 (PD-1) antibody plus vascular endothelial growth factor receptor tyrosine kinase inhibitor (VEGFR-TKI) failed to prevent disease progression. However, a regimen of anti-PD-1 plus anti-cytotoxic t-lymphocyte associated protein 4 (CTLA-4) reversed the progression to a complete response. This case shows that METex14 had a significant response to immunotherapy, which would be especially beneficial for those who developed targeted therapy resistance. Importantly, this is the first case reporting that salvage CTLA-4 antibody and PD-1 antibody could reverse the progression in NSCLC harboring METex14 when the anti-PD-1 resistance occurred.
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