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

被引:7
|
作者
Zhu, Viola W. [1 ]
Schrock, Alexa B. [2 ]
Bosemani, Thangavijayan [3 ]
Benn, Bryan S. [4 ]
Ali, Siraj M. [2 ]
Ou, Sai-Hong Ignatius [1 ]
机构
[1] Univ Calif Irvine, Sch Med, Dept Med, Chao Family Comprehens Canc Ctr,Div Hematol Oncol, 101 City Dr South, Orange, CA 92868 USA
[2] Fdn Med Inc, Clin Dev, Cambridge, MA USA
[3] Univ Calif Irvine, Sch Med, Dept Radiol Sci, Orange, CA 92668 USA
[4] Univ Calif Irvine, Sch Med, Dept Med, Div Pulm Dis & Crit Care Med, Orange, CA 92668 USA
来源
关键词
VKORC1L1; T1151; fusion; resistance; crizotinib; lorlatinib;
D O I
10.2147/LCTT.S186804
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
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.
引用
收藏
页码:111 / 116
页数:6
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