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病例报告:非小细胞肺癌中的伴随突变和重排

Case report: Concomitant mutation and rearrangement in non-small cell lung cancer.

作者信息

Hu Haoyue, Tan Songtao, Xie Meng, Guo Peng, Yu Qiang, Xiao Juan, Zhao Kangrui, Liao Qiong, Wang Yi

机构信息

Department of Radiation Oncology, Sichuan Clinical Research Center for Cancer, Sichuan Cancer Hospital and Institute, Sichuan Cancer Center, Affiliated Cancer Hospital of University of Electronic Science and Technology of China, Chengdu, China.

West China School of Medicine, Sichuan University, Chengdu, China.

出版信息

Front Pharmacol. 2023 Aug 29;14:1167959. doi: 10.3389/fphar.2023.1167959. eCollection 2023.

Abstract

In non-small cell lung cancer (NSCLC), two key genetic alterations, epidermal growth factor receptor () mutations and anaplastic lymphoma kinase () rearrangements, are commonly believed to be mutually exclusive. Studies have reported that concurrent co-mutation in non-small cell lung cancer patients is rare, with a prevalence ranging from 0.1% to 1.6%. However, the clinical and pathological characteristics of these patients are not well-defined, and the optimal treatment approach for such cases remains controversial. In this report, we present a case of stage IV lung adenocarcinoma with both epidermal growth factor receptor and anaplastic lymphoma kinase mutations, along with high PD-L1 expression. The patient initially received treatment with epidermal growth factor receptor tyrosine kinase inhibitors (TKIs), but the disease progressed. However, following a switch to -TKI therapy and local radiotherapy, the lesion showed regression. Our report also provides a comprehensive summary of the clinical and pathological features, as well as treatment strategies, for non-small cell lung cancer patients with concurrent epidermal growth factor receptor mutation and anaplastic lymphoma kinase rearrangement.

摘要

在非小细胞肺癌(NSCLC)中,两种关键的基因改变,即表皮生长因子受体(EGFR)突变和间变性淋巴瘤激酶(ALK)重排,通常被认为是相互排斥的。研究报告称,非小细胞肺癌患者中EGFR共突变的情况很少见,发生率在0.1%至1.6%之间。然而,这些患者的临床和病理特征尚不明确,此类病例的最佳治疗方法仍存在争议。在本报告中,我们展示了一例IV期肺腺癌病例,该病例同时存在表皮生长因子受体和间变性淋巴瘤激酶突变,以及高程序性死亡配体1(PD-L1)表达。患者最初接受表皮生长因子受体酪氨酸激酶抑制剂(TKIs)治疗,但疾病进展。然而,在改用ALK-TKI治疗和局部放疗后,病灶出现消退。我们的报告还全面总结了同时存在表皮生长因子受体突变和间变性淋巴瘤激酶重排的非小细胞肺癌患者的临床和病理特征以及治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c9ad/10495838/a0429a8c0788/fphar-14-1167959-g001.jpg

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