Efficacy generated by afatinib in a lung adenocarcinoma patient harboring HER2 S310Y mutation

被引:8
|
作者
Wang, Jian [1 ]
Wen, Yuxin [1 ]
Ding, Guanggui [1 ]
Ding, Peikun [1 ]
Zhang, Lu [2 ]
Liu, Jing [2 ]
Zhang, Tengfei [2 ]
Yang, Lin [1 ]
机构
[1] Jinan Univ, Clin Med Coll 2, Shenzhen Peoples Hosp, Dept Thorac Surg, 1017 North Dongmen Rd, Shenzhen 518020, Peoples R China
[2] Burning Rock Biotech, 7 Luoxuan 4th Rd, Guangzhou, Guangdong, Peoples R China
关键词
adenocarcinoma; HER2; S310Y; afatinib; next-generation sequencing; targeted therapy; TYROSINE KINASE MUTATIONS; BREAST-CANCER; ERBB2; PREVALENCE; MUTANT; DOMAIN;
D O I
10.1080/15384047.2018.1449611
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Afatinib exhibits therapeutic efficacy for lung adenocarcinoma patients harboring HER2 exon 20 insertions. HER2 S310Y single site substitution was discovered in recent years and afatinib efficacy for adenocarcinoma patients harboring S310Y mutation has not been reported. We presented a case of a 41-year-old male patient with lung adenocarcinoma harboring the HER2 S310Y mutation obtained clinical response to the treatment of afatinib, an oral HER family blocker. After the treatment of afatinib, the patient achieved partial response (PR) in chest lesions and almost complete response (CR) in intracranial lesions. He experienced progressive disease (PD) with liver metastasis and achieved a progression-free survival (PFS) of 5 months. He continually treated with afatinib after CT guided percutaneous radiofrequency ablation to eradicate the hepatic tumor cells and achieved stable disease (SD). In this study, we reported the first clinical evidence of efficacy generated by afatinib, the irreversible HER family inhibitor, targeting HER2 S310Y single site mutation in lung adenocarcinoma.
引用
收藏
页码:450 / 453
页数:4
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