Second generation tyrosine kinase inhibitors for the treatment of metastatic non-small-cell lung cancer.

Translational respiratory medicine Pub Date : 2014-01-06 eCollection Date: 2014-01-01 DOI:10.1186/2213-0802-2-2
Irene Stasi, Federico Cappuzzo
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引用次数: 23

Abstract

Backgruond: Since their first description, activating epidermal growth factor receptor (EGFR) mutations identify a distinct clinical entity of patients with non-small-cell lung cancer (NSCLC).

Findings: New targeted therapies for molecularly selected NSCLC are changing the natural history of the disease, with results superior to standard chemotherapy as demonstrated in large phase III studies with first generation EGFR tyrosine kinase inhibitors (TKIs) erlotinib and gefitinib. However, after an initial response, all patients inevitably progress and several mechanisms including a secondary mutation in exon 20 of the EGFR gene (T790M) or MET or HER2 amplifications are responsible for acquired resistance (AR). In clinical practice few options are available for patients with AR, and several new agents or strategies are currently under investigation, including second generation TKIs.

Conclusions: Aim of the present review is to present available data on new EGFR-TKIs and to discuss how these agents could overcome AR to erlotinib or gefitinib.

Abstract Image

Abstract Image

第二代酪氨酸激酶抑制剂治疗转移性非小细胞肺癌。
背景:自首次描述以来,激活表皮生长因子受体(EGFR)突变确定了非小细胞肺癌(NSCLC)患者的独特临床实体。研究结果:分子选择性非小细胞肺癌的新靶向治疗正在改变疾病的自然史,其结果优于使用第一代EGFR酪氨酸激酶抑制剂(TKIs)厄洛替尼和吉非替尼的大型III期研究。然而,在最初的反应之后,所有患者不可避免地会出现进展,包括EGFR基因20外显子的继发性突变(T790M)或MET或HER2扩增在内的几种机制是获得性耐药(AR)的原因。在临床实践中,AR患者的选择很少,目前正在研究几种新的药物或策略,包括第二代tki。结论:本综述的目的是提供新的EGFR-TKIs的可用数据,并讨论这些药物如何克服对厄洛替尼或吉非替尼的反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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