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Drug Resistance to Molecular Targeted Therapy and Its Consequences for Treatment Decisions in Non-Small-Cell Lung Cancer

机译:非小细胞肺癌对分子靶向疗法的耐药性及其治疗决策的后果

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摘要

Our ability to detect and directly target the oncogenic alterations responsible for tumor proliferation has contributed significantly to the management of lung cancer in the last decade. The therapeutic efficacy of molecularly targeted therapy is, however, mainly limited to patients harboring certain genetic mutations and is generally short-lived. Herein, we review primary and secondary drug resistance using the most well-studied of the molecularly targeted agents, the tyrosine kinase inhibitors targeting the epidermal growth factor (EGF) receptor, and the anaplastic lymphoma kinase (ALK) rearrangement, the current limitations of targeted therapies and their consequences on the management of patients with lung cancer.
机译:在过去的十年中,我们检测并直接靶向导致肿瘤增殖的致癌性改变的能力为肺癌的治疗做出了重要贡献。然而,分子靶向疗法的治疗功效主要限于具有某些遗传突变的患者,并且通常寿命短。本文中,我们使用研究最深入的分子靶向药物,靶向表皮生长因子(EGF)受体的酪氨酸激酶抑制剂和间变性淋巴瘤激酶(ALK)重排(针对靶向药物的当前局限性),对原发性和继发性药物耐药性进行了综述疗法及其对肺癌患者治疗的影响。

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