首页> 美国卫生研究院文献>Lung Cancer: Targets and Therapy >Dramatic response to alectinib in a lung cancer patient with a novel VKORC1L1-ALK fusion and an acquired ALK T1151K mutation
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Dramatic response to alectinib in a lung cancer patient with a novel VKORC1L1-ALK fusion and an acquired ALK T1151K mutation

机译:患有新型VKORC1L1-ALK融合和获得性ALK T1151K突变的肺癌患者对爱乐替尼的剧烈反应

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摘要

ALK-rearranged lung cancer defines a distinctive molecular cohort of patients whose outcomes are significantly improved by the availability of ALK inhibitors. Thus, it is imperative for clinicians to screen appropriate patients for this driver mutation with a molecular testing platform capable of capturing all ALK fusions. Here, we report a novel VKORC1L1-ALK fusion and an ALK T1151K resistance mutation detected in a lung cancer patient who had been on crizotinib for over 8 years. Alectinib induced a dramatic response in this patient demonstrating its clinical activity against T1151K. This case illustrates the importance of performing repeat biopsy to explore mechanism(s) of resistance when patients experience disease progression on an ALK inhibitor. The approach has a direct therapeutic impact particularly when an ALK resistance mutation is identified.
机译:ALK重排的肺癌定义了患者的独特分子队列,这些患者的病因可通过ALK抑制剂获得显着改善。因此,对于临床医生而言,必须使用能够捕获所有ALK融合蛋白的分子测试平台来筛选适合该驱动程序突变的合适患者。在这里,我们报告了一种新的VKORC1L1-ALK融合和ALK T1151K耐药性突变,该患者在使用克唑替尼治疗8年以上的肺癌患者中检测到。艾乐替尼在该患者中引起了剧烈反应,表明其针对T1151K的临床活性。该案例说明了当患者在ALK抑制剂上经历疾病进展时,进行重复活检以探索耐药机制的重要性。该方法具有直接的治疗效果,尤其是在鉴定出ALK抗性突变时。

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