HER2 Exon 20 Insertion Mutations in Lung Adenocarcinoma: Case Series and Response to Pyrotinib

被引:7
|
作者
Zhang, Xinyong [1 ]
Lv, Jialin [1 ]
Wu, Yuhua [1 ]
Qin, Na [1 ]
Ma, Li [1 ]
Li, Xi [1 ]
Nong, Jingying [1 ]
Zhang, Hui [1 ]
Zhang, Quan [1 ]
Yang, Xinjie [1 ]
Shi, Huibo [2 ]
Wang, Jinghui [1 ]
Zhang, Shucai [1 ]
机构
[1] Capital Med Univ, Beijing Chest Hosp, Dept Med Oncol, Beijing TB & Thorac Tumor Res Inst, Beijing, Peoples R China
[2] Huazhong Univ Sci & Technol, Tongji Med Coll, Tongji Hosp, Organ Transplantat Res Inst, Wuhan, Peoples R China
来源
FRONTIERS IN ONCOLOGY | 2020年 / 10卷
关键词
lung adenocarcinoma; human epidermal growth factor receptor 2; exon; 20; driver oncogenes; pyrotinib; PHASE-II; CANCER; AFATINIB; CHEMOTHERAPY; COMBINATION; CRIZOTINIB; OUTCOMES;
D O I
10.3389/fonc.2020.01162
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
HER2 mutations have emerged as oncogenic driver gene mutations in non-small cell lung cancer (NSCLC), which have not been described in detail like other driver gene mutations. Here, 295 patients with advanced lung adenocarcinoma were retrospectively screened for HER2 mutations using next-generation sequencing (NGS), and the positive cases were validated by Sanger sequencing. We identified five cases with HER2 exon 20 insertions, representing 1.7% of 295 lung adenocarcinomas. Among them, four different subtypes of HER2 exon 20 insertions were identified, including a rare subtype G778_S779insCPG never reported before with a partial response (PR) to pyrotinib and progression-free survival (PFS) of 12.8 months. Our findings reveal that HER2 exon 20 insertion mutations were detected in a small subset of lung adenocarcinomas. Given the different drug sensitivities, determining the mutation subtype by next-generation sequencing at the time of diagnosis might make sense.
引用
收藏
页数:6
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