| Article ID | Journal | Published Year | Pages | File Type | 
|---|---|---|---|---|
| 8453783 | Lung Cancer | 2018 | 4 Pages | 
Abstract
												Missense mutations in EGFR exon 20 are rare in non-small-cell lung cancer (NSCLC), and mostly insensitive to the first generation tyrosine kinase inhibitors (TKIs) of EGFR. However, their responses to the third generation TKI are unclear. Here, we reported a patient with advanced NSCLC harboring a rare EGFR H773L/V774M mutation complex. Although he was irresponsive to the first generation TKI gefitinib, he demonstrated sustained disease control to osimertinib, suggesting that this complex is an activating mutation of EGFR and can be suppressed by osimertinib. The follow-up genetic profiling revealed multiple acquired new mutations that might be related to his resistance to osimertinib. This finding would provide valuable experience for future treatment of the same mutations.
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											Authors
												Minglei Yang, Xiaoling Tong, Xiang Xu, Enkuo Zheng, Junjun Ni, Junfang Li, Junrong Yan, Yang W. Shao, Guofang Zhao, 
											