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表皮生长因子受体(p.G719A+L747V)/棘皮动物微管相关蛋白样4-间变性淋巴瘤激酶共改变的肺腺癌伴软脑膜转移对阿法替尼治疗有反应:一例报告

EGFR (p. G719A+L747V)/EML4-ALK Co-alterations in Lung Adenocarcinoma with Leptomeningeal Metastasis Responding to Afatinib Treatment: A Case Report.

作者信息

Lu Zhiqin, Wang Xia, Luo Yuxi, Wei Jianping, Zeng Zhimin, Xiong Qiang, Cai Jing, Liu Anwen

机构信息

Department of Oncology, The Second Affiliated Hospital of Nanchang University, Nanchang, Jiangxi Province, People's Republic of China.

Jiangxi Key Laboratory of Clinical Translational Cancer Research, Nanchang, Jiangxi Province, People's Republic of China.

出版信息

Onco Targets Ther. 2021 Apr 23;14:2823-2828. doi: 10.2147/OTT.S294635. eCollection 2021.

Abstract

Leptomeningeal metastasis (LM) is a disastrous complication of advanced lung adenocarcinoma (LAC) associated with poor prognosis and rapid deterioration of performance status. The prevalence of epidermal growth factor receptor (EGFR)/anaplastic lymphoma kinase (ALK) co-alterations in patients with LAC was low. Herein, we report a patient with alterations in both EGFR (p. G719A+L747V) and echinoderm microtubule-associated protein-like ALK (EML4-ALK) fusion and LM who was treated with afatinib. The patient's clinical symptoms improved, and imaging examination revealed reduced intracranial and extracranial lesions. The progression-free survival (PFS) using afatinib for LM was 25 months, and no severe adverse events occurred.

摘要

软脑膜转移(LM)是晚期肺腺癌(LAC)的灾难性并发症,预后较差,身体状况迅速恶化。LAC患者中表皮生长因子受体(EGFR)/间变性淋巴瘤激酶(ALK)共改变的发生率较低。在此,我们报告1例EGFR(p.G719A+L747V)和棘皮动物微管相关蛋白样ALK(EML4-ALK)融合均有改变且发生LM的患者,该患者接受了阿法替尼治疗。患者的临床症状改善,影像学检查显示颅内和颅外病变减少。使用阿法替尼治疗LM的无进展生存期(PFS)为25个月,未发生严重不良事件。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/19b7/8079359/7b1ccae55731/OTT-14-2823-g0001.jpg

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