Dramatic response to alectinib in a lung cancer patient with a novel VKORC1L1-ALK fusion and an acquired ALK T1151K mutation.

IF 5.1 Q1 ONCOLOGY Lung Cancer: Targets and Therapy Pub Date : 2018-11-08 DOI:10.2147/LCTT.S186804
Viola W Zhu, Alexa B Schrock, Thangavijayan Bosemani, Bryan S Benn, Siraj M Ali, Sai-Hong Ignatius Ou
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引用次数: 9

Abstract

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.

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一名具有新型VKORC1L1-ALK融合物和获得性ALK T1151K突变的癌症患者对阿来替尼的显著反应。
ALK排列的癌症定义了一个独特的患者分子队列,其结果因ALK抑制剂的可用性而显著改善。因此,临床医生必须使用能够捕获所有ALK融合的分子测试平台来筛选合适的患者以检测这种驱动突变。在此,我们报道了一种新型VKORC1L1-ALK融合物和一种ALK T1151K耐药性突变,该突变在一名服用克唑替尼超过8年的癌症患者中检测到。Alectinib在该患者中诱导了显著的反应,证明了其对T1151K的临床活性。该病例说明了当患者在ALK抑制剂上经历疾病进展时,进行重复活检以探索耐药性机制的重要性。该方法具有直接的治疗效果,特别是当发现ALK耐药性突变时。
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来源期刊
CiteScore
8.10
自引率
0.00%
发文量
10
审稿时长
16 weeks
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