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Overcoming resistance to targeted therapies in NSCLC: current approaches and clinical application

机译:克服非小细胞肺癌靶向治疗的耐药性:当前方法和临床应用

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摘要

The discovery that a number of aberrant tumorigenic processes and signal transduction pathways are mediated by druggable protein kinases has led to a revolutionary change in nonsmall cell lung cancer (NSCLC) treatment. Epidermal growth factor receptor (EGFR) and anaplastic lymphoma kinase (ALK) are the targets of several tyrosine kinase inhibitors (TKIs), some of them approved for treatment and others currently in clinical development. First-generation agents offer, in target populations, a substantial improvement of outcomes compared with standard chemotherapy in the treatment of advanced NSCLC. Unfortunately, drug resistance develops after initial benefit through a variety of mechanisms. Novel generation EGFR and ALK inhibitors are currently in advanced clinical development and are producing encouraging results in patients with acquired resistance to previous generation agents. The search for new drugs or strategies to overcome the TKI resistance in patients with EGFR mutations or ALK rearrangements is to be considered a priority for the improvement of outcomes in the treatment of advanced NSCLC.
机译:可药用蛋白激酶介导许多异常的致瘤过程和信号转导途径的发现已导致非小细胞肺癌(NSCLC)治疗的革命性变化。表皮生长因子受体(EGFR)和间变性淋巴瘤激酶(ALK)是几种酪氨酸激酶抑制剂(TKI)的靶标,其中一些已获批准用于治疗,其他已在临床开发中。与标准化疗相比,第一代药物在目标人群中可显着改善晚期NSCLC的治疗效果。不幸的是,在通过多种机制获得最初的收益后,耐药性逐渐增强。新一代EGFR和ALK抑制剂目前处于先进的临床开发中,并且在对前几代药物产生耐药性的患者中产生令人鼓舞的结果。在EGFR突变或ALK重排的患者中寻找新的药物或策略以克服TKI抵抗被认为是改善晚期NSCLC治疗结果的优先事项。

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