Efficacy of Pyrotinib in a Heavily Pretreated Patient with Lung Adenocarcinoma Harboring HER2 Amplification and Exon 20 Insertions: A Case Report

被引:2
|
作者
Shan, Jianzhen [1 ]
Ruan, Jian [1 ]
Tan, Yanbin [2 ]
Yan, Li [3 ]
Chen, Songan [3 ]
Du, Miaoyan [1 ]
Wang, Lingjie [1 ]
机构
[1] Zhejiang Univ, Sch Med, Affiliated Hosp 1, Dept Med Oncol, Hangzhou, Peoples R China
[2] Zhejiang Univ, Sch Med, Dept Radiol, Affiliated Hosp 2, Hangzhou, Peoples R China
[3] Burning Rock Biotech, Dept Med, Guangzhou, Peoples R China
来源
ONCOTARGETS AND THERAPY | 2020年 / 13卷
关键词
pyrotinib; HER2; mutation; amplification; non-small cell lung cancer; next-generation sequencing; TYROSINE KINASE INHIBITOR; MUTATION; DRIVERS; CANCERS;
D O I
10.2147/OTT.S271999
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The clinical benefits of HER2 inhibitors in patients with non-small cell lung cancer (NSCLC) have been limited. There is a paucity of effective therapies in NSCLC after developing resistance to initial anti-HER2 therapy. Herein, we presented the clinical benefit of pyrotinib in a 53-year-old patient with advanced lung adenocarcinoma whose circulating tumor DNA (ctDNA) analysis of pleural effusion revealed the coexistence of HER2 exon 20 p.Y772_A775dup (mutation ratio: 38.86%) and HER2 amplification (copy number: 4.5) following failures of multiple therapies including afatinib and ado-trastuzumab emtansine (T-DM1). Notably, pyrotinib treatment induced rapid and marked improvement of clinical symptoms, and partial response was observed after 8 weeks. CtDNA monitoring during the treatment showed that the mutation ratio of HER2 decreased to 7.99%, and the amplification disappeared. The patient achieved a progression-free survival of 7.5 months after treatment with pyrotinib. Thus, pyrotinib may be a new treatment strategy for the subgroup of lung adenocarcinoma patients, with coexistence of HER2 exon 20 p.Y772_A775dup and HER2 amplification even after failures of multiple anti-HER2 therapies. It also indicated the value of capture-based next-generation sequencing to monitor and guide therapy.
引用
收藏
页码:9849 / 9856
页数:8
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