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非小细胞肺癌中的复杂种系K757N突变:一例报告

Complex Germline K757N Mutation in Non-Small-Cell Lung Cancer: A Case Report.

作者信息

Wong Boaz, Moore Sara, Wheatley-Price Paul

机构信息

Department of Biochemistry, Microbiology and Immunology, Faculty of Medicine, University of Ottawa, Ottawa, Ontario, Canada.

Cancer Therapeutics Program, Ottawa Hospital Research Institute, Ottawa, Ontario, Canada.

出版信息

Case Rep Oncol. 2022 Mar 21;15(1):285-290. doi: 10.1159/000523734. eCollection 2022 Jan-Apr.

Abstract

Epidermal growth factor receptor (EGFR) mutations are usually oncogenic drivers of lung tumor development and progression. While common sensitizing mutations respond well to targeted therapy, the relevance of germline EGFR mutations is less clear. We describe a 65-year-old, previously healthy, male diagnosed with non-small-cell lung cancer. Familial history for lung cancer is negative. Targeted next-generation sequencing on the tumor biopsy sample revealed an atypical EGFR K757N mutation at 50% allele frequency and genetic review of a previously acquired gastric sample confirms the mutation as a germline change. He received standard first-line chemoimmunotherapy with carboplatin, pemetrexed, and pembrolizumab, and after 8 months therapy continues, with stable disease, to receive maintenance pemetrexed and pembrolizumab. To our knowledge, this is the first report of an atypical, germline K757N EGFR mutation. While the clinical relevance of this mutation is unclear, standard reporting of the allelic frequency of novel, atypical mutations can detect potential germline changes.

摘要

表皮生长因子受体(EGFR)突变通常是肺肿瘤发生和进展的致癌驱动因素。虽然常见的敏感突变对靶向治疗反应良好,但种系EGFR突变的相关性尚不清楚。我们描述了一名65岁、既往健康的男性,被诊断为非小细胞肺癌。肺癌家族史为阴性。对肿瘤活检样本进行的靶向二代测序显示,存在一个非典型的EGFR K757N突变,等位基因频率为50%,对先前获取的胃样本进行的基因检测证实该突变为种系改变。他接受了以卡铂、培美曲塞和帕博利珠单抗为主的标准一线化疗免疫治疗,治疗8个月后病情持续稳定,继续接受培美曲塞和帕博利珠单抗维持治疗。据我们所知,这是首例非典型种系K757N EGFR突变的报告。虽然该突变的临床相关性尚不清楚,但对新型非典型突变的等位基因频率进行标准报告可检测潜在的种系改变。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b20/9035954/e342ec5261a5/cro-0015-0285-g01.jpg

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