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首页> 外文期刊>Lung Cancer: Targets and Therapy >A Comprehensive Review of Contemporary Literature for Epidermal Growth Factor Receptor Tyrosine Kinase Inhibitors in Non-Small Cell Lung Cancer and Their Toxicity
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A Comprehensive Review of Contemporary Literature for Epidermal Growth Factor Receptor Tyrosine Kinase Inhibitors in Non-Small Cell Lung Cancer and Their Toxicity

机译:非小细胞肺癌表皮生长因子受体酪氨酸激酶抑制剂的全面综述及其毒性

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Mutations in the epidermal growth factor receptor (EGFR) are common amongst those with non-small cell lung cancer and represent a major factor in treatment decisions, most notably in the advanced stages. Small molecule tyrosine kinase inhibitors (TKIs) that target the EGFR, such as erlotinib, gefitinib, icotinib, afatinib, dacomitinib and osimertinib, have all shown to be effective in this setting. Osimertinib, a third-generation EGFR TKI, is a favorable option, but almost all patients develop resistance at some time point. There are no effective treatment options for patients who progress on osimertinib, but ongoing trials will hopefully address this unmet need. The aim of this review is to provide a comprehensive review of the data with EGFR TKIs, management of the toxicities and the ongoing trials with this class of agents.
机译:表皮生长因子受体(EGFR)中的突变在具有非小细胞肺癌的那些中是常见的,并且代表治疗决策的主要因素,最值得注意的是在先进阶段。靶向EGFR的小分子酪氨酸激酶抑制剂(TKIS),例如Erlotinib,Gefitinib,Icotinib,Afatinib,Dacomitinib和Osimertinib,所有如此在该设置中都被证明是有效的。 Osimertinib是第三代EGFR TKI,是一个有利的选择,但几乎所有患者在某个时间点都会产生抗性。对于Osimertinib的患者而言,没有有效的治疗选择,但正在进行的审判希望解决这种未满足的需求。本综述的目的是提供与EGFR TKI的数据进行全面审查,毒性管理以及与这类代理商的持续审判。

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