Treatment Response To Osimertinib In EGFR-Mutated Leptomeningeal Metastases From Non-Small Cell Lung Cancer: A Case Series

被引:6
|
作者
Li, Huiying [1 ]
Yu, Tingting [1 ]
Huang, Mingmin [1 ]
Guo, Aibin [1 ]
Qian, Xiaoping [2 ]
Yin, Zhenyu [1 ]
机构
[1] Nanjing Univ, Med Sch, Affiliated Nanjing Drum Tower Hosp, Dept Geriatr Oncol, 321 Zhongshan Rd, Nanjing 210008, Jiangsu, Peoples R China
[2] Nanjing Univ, Comprehens Canc Ctr, Drum Tower Hosp, Clin Canc Inst, 321 Zhongshan Rd, Nanjing 210008, Jiangsu, Peoples R China
来源
ONCOTARGETS AND THERAPY | 2019年 / 12卷
关键词
non-small cell lung cancer; leptomeningeal metastases; osimertinib; EGFR mutation; T790M; GROWTH-FACTOR RECEPTOR; CEREBROSPINAL-FLUID; BRAIN METASTASES; NSCLC; CARCINOMATOSIS; RESISTANCE; NIVOLUMAB; PATIENT;
D O I
10.2147/OTT.S199452
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
Therapy for leptomeningeal metastases (LM) from non-small cell lung cancer (NSCLC) is challenging, and conventional treatments have little impact on the disease course. We report three cases that were definitively diagnosed as LM from NSCLC with a mutation of epidermal growth factor receptor (EGFR) L858R. The systemic therapies of chemotherapy, local radiotherapy, and early generation tyrosine kinase inhibitors (TKIs) were implemented but ineffective. Three patients were treated with the third-generation TKI osimertinib at 80 mg daily, despite their different detection levels of T790M in the cerebrospinal fluid (CSF) and plasma, and achieved symptomatic remission, a decline of carcinoembryonic antigen (CEA) levels, and stable lesions. After the progression of LM, osimertinib at 160 mg daily further lengthened the quality of life and survival time of patients without any notable side effects during treatment. Recent related studies and our cases indicate that osimertinib has a positive effect on LM from EGFR-mutant NSCLC, regardless of T790M status.
引用
收藏
页码:7785 / 7790
页数:6
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