聚焦特泊替尼和卡马替尼治疗MET 14外显子跳越突变的非小细胞肺癌。

IF 5.1 Q1 ONCOLOGY Lung Cancer: Targets and Therapy Pub Date : 2022-05-13 eCollection Date: 2022-01-01 DOI:10.2147/LCTT.S360574
Danielle Brazel, Shannon Zhang, Misako Nagasaka
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引用次数: 0

摘要

间质-上皮转化(MET)受体酪氨酸激酶在 1-20% 的 NSCLC 中过度表达、扩增或突变。MET 失调与预后不良有关。最近,针对 MET 14 号外显子突变的靶向疗法在早期试验中显示出了疗效和耐受性。在此,我们将重点介绍特泊替尼(tepotinib)和卡马替尼(capmatinib)的分子特征、早期临床前和临床数据以及在未来研究和临床实践中的新作用。
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Spotlight on Tepotinib and Capmatinib for Non-Small Cell Lung Cancer with MET Exon 14 Skipping Mutation.

Mesenchymal-epithelial transition (MET) receptor tyrosine kinase is overexpressed, amplified, or mutated in 1-20% of NSCLC. MET dysregulation is associated with a poor prognosis. Recently, development of targeted therapies against MET exon 14 mutations has demonstrated efficacy and tolerability in early trials. Here we focus on tepotinib and capmatinib in regards to molecular characteristics, early preclinical and clinical data, and the emerging role in future studies and clinical practice.

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来源期刊
CiteScore
8.10
自引率
0.00%
发文量
10
审稿时长
16 weeks
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