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Mechanisms of Epidermal Growth Factor Receptor Tyrosine Kinase Inhibitor Resistance and Strategies to Overcome Resistance in Lung Adenocarcinoma

机译:表皮生长因子受体酪氨酸激酶抑制剂的耐药机制及克服策略在肺腺癌中的抵抗。

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摘要

Somatic mutations that lead to hyperactivation of epidermal growth factor receptor (EGFR) signaling are detected in approximately 50% of lung adenocarcinoma in people from the Far East population and tyrosine kinase inhibitors are now the standard first line treatment for advanced disease. They have led to a doubling of progression-free survival and an increase in overall survival by more than 2 years. However, emergence of resistant clones has become the primary cause for treatment failure, and has created a new challenge in the daily management of patients with EGFR mutations. Identification of mechanisms leading to inhibitor resistance has led to new therapeutic modalities, some of which have now been adapted for patients with unsuccessful tyrosine kinase inhibitor treatment. In this review, we describe mechanisms of tyrosine kinase inhibitor resistance and the available strategies to overcoming resistance.
机译:在远东人群中约50%的肺腺癌中检测到导致表皮生长因子受体(EGFR)信号过度活化的体细胞突变,酪氨酸激酶抑制剂现已成为晚期疾病的标准一线治疗方法。它们使无进展生存期增加了一倍,总体生存期增加了2年以上。然而,抗性克隆的出现已成为治疗失败的主要原因,并在EGFR突变患者的日常管理中提出了新的挑战。鉴定导致抑制剂抗性的机制已经导致了新的治疗方式,其中一些现已被用于酪氨酸激酶抑制剂治疗失败的患者。在这篇综述中,我们描述了酪氨酸激酶抑制剂耐药性的机制以及克服耐药性的可用策略。

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