用酪氨酸激酶抑制剂治疗egfr突变的非小细胞肺癌患者的轻脑膜疾病的影像学表现:一个病例系列

Q1 Medicine
CNS Oncology Pub Date : 2019-06-20 DOI:10.2217/cns-2019-0010
Ugur T Sener, Nassim Matin, H. Yu, A. Lin, T. Yang, R. Malani
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引用次数: 3

摘要

EGFR在非小细胞肺癌(nsclc)中经常发生突变。临床可用的酪氨酸激酶抑制剂(TKIs)对治疗egfr突变型NSCLC有效。在本病例系列中,我们报告了5例经tki治疗的egfr突变的NSCLC患者,他们发展为缺乏特征性影像学发现的轻脑膜病(LMD)。所有5例患者在发生细胞学证实的LMD之前都接受了tki治疗。LMD的临床症状比影像学证据早2-12个月。T790M是对第一代EGFR抑制剂最常见的耐药突变,在4例中被发现。这些病例表明,在egfr突变的NSCLC患者中,TKIs可以有效地控制LMD,造成症状发作和观察影像学表现之间的滞后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Radiographic appearance of leptomeningeal disease in patients with EGFR-mutated non-small-cell lung carcinoma treated with tyrosine kinase inhibitors: a case series
EGFR is frequently mutated in non-small-cell lung carcinomas (NSCLCs). Clinically available tyrosine kinase inhibitors (TKIs) are effective in treating EGFR-mutant NSCLC. In this case series, we present five patients with TKI-treated EGFR-mutated NSCLC who developed leptomeningeal disease (LMD) lacking characteristic imaging findings. All five patients received TKIs prior to development of cytology-confirmed LMD. Clinical signs of LMD preceded radiographic evidence by 2–12 months. T790M, the most common resistance mutation to first-generation EGFR inhibitors, was identified in four cases. These cases illustrate that in patients with EGFR-mutant NSCLC, TKIs may effectively control LMD, creating a lag between onset of symptoms and observation of radiographic findings.
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来源期刊
CNS Oncology
CNS Oncology Medicine-Neurology (clinical)
CiteScore
3.80
自引率
0.00%
发文量
12
审稿时长
13 weeks
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