Suppr超能文献

一名中国肺腺癌患者中对克唑替尼产生反应的新型c-间充质-上皮转化因子基因间融合:病例报告

A Novel c-Mesenchymal-Epithelial Transition Factor Intergenic Fusion Response to Crizotinib in a Chinese Patient With Lung Adenocarcinoma: A Case Report.

作者信息

Liang Hongge, Zhou Dexun, Dai Lin, Zhang Moqin, Gao Zhancheng, Mu Xinlin

机构信息

Department of Respiratory and Critical Care Medicine, Peking University People's Hospital, Beijing, China.

Department of Pathology, Peking University People's Hospital, Beijing, China.

出版信息

Front Oncol. 2021 Oct 28;11:727662. doi: 10.3389/fonc.2021.727662. eCollection 2021.

Abstract

BACKGROUND

The c-mesenchymal-epithelial transition factor (C-MET) is an oncogene encoding a tyrosine kinase receptor that plays an important role in tumor growth and metastasis. The National Comprehensive Cancer Network (NCCN) guidelines have approved carbatinib/crizotinib for advanced non-small cell lung cancer (NSCLC) patients with MET exon 14 skipping.

METHODS

In June 2020, the Department of Respiratory and Critical Care Medicine of Peking University People's Hospital admitted a 72-year-old male patient with lung adenocarcinoma (LADC) with a history of interstitial lung disease secondary to antineutrophil cytoplasmic antibody-associated vasculitis. Genetic examination by next-generation sequencing showed an intergenic fusion of MET, and crizotinib was administered on August 14, 2020. Follow-up showed that tumor volume was significantly reduced. However, crizotinib was discontinued in November 2020 because of the patient's worsening interstitial lung disease, and CT scans showed continued partial response (PR) for 5 months. In April 2021, right lower lobe mass progressed, and disease progression was considered.

CONCLUSION

This was the first case of a patient with LADC with MET intergenic fusion who significantly benefited from crizotinib. Even after crizotinib was discontinued for 5 months, the patient continued exhibiting PR, suggesting that MET intergenic fusion may have carcinogenic activity in LADC and was sensitive to crizotinib.

摘要

背景

c-间充质-上皮转化因子(C-MET)是一种编码酪氨酸激酶受体的致癌基因,在肿瘤生长和转移中起重要作用。美国国立综合癌症网络(NCCN)指南已批准卡博替尼/克唑替尼用于治疗具有MET外显子14跳跃的晚期非小细胞肺癌(NSCLC)患者。

方法

2020年6月,北京大学人民医院呼吸与危重症医学科收治了一名72岁男性肺腺癌(LADC)患者,该患者有抗中性粒细胞胞浆抗体相关性血管炎继发的间质性肺疾病病史。通过下一代测序进行的基因检测显示MET基因间融合,于2020年8月14日给予克唑替尼治疗。随访显示肿瘤体积显著缩小。然而,由于患者间质性肺疾病恶化,克唑替尼于2020年11月停药,CT扫描显示持续部分缓解(PR)达5个月。2021年4月,右下叶肿块进展,考虑疾病进展。

结论

这是首例LADC合并MET基因间融合且从克唑替尼中显著获益的患者。即使克唑替尼停药5个月后,患者仍持续表现出PR,提示MET基因间融合可能在LADC中具有致癌活性且对克唑替尼敏感。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3cca/8581303/6f0c937c67f8/fonc-11-727662-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验