Novel CAD-ALK gene rearrangement is drugable by entrectinib in colorectal cancer

被引:65
作者
Amatu, Alessio [1 ]
Somaschini, Alessio [2 ]
Cerea, Giulio [1 ]
Bosotti, Roberta [2 ]
Valtorta, Emanuele [1 ]
Buonandi, Pasquale [1 ]
Marrapese, Giovanna [1 ]
Veronese, Silvio [1 ]
Luo, David [3 ]
Hornby, Zachary [3 ]
Multani, Pratik [3 ]
Murphy, Danielle [3 ]
Shoemaker, Robert [3 ]
Lauricella, Calogero [1 ]
Giannetta, Laura [1 ]
Maiolani, Martina [1 ]
Vanzulli, Angelo [1 ]
Ardini, Elena [2 ]
Galvani, Arturo [2 ]
Isacchi, Antonella [2 ]
Sartore-Bianchi, Andrea [1 ]
Siena, Salvatore [1 ,4 ]
机构
[1] Osped Niguarda Ca Granda, Niguarda Canc Ctr, I-20162 Milan, Italy
[2] Nerviano Med Sci Srl, Business Unit Oncol, I-20014 Nerviano, MI, Italy
[3] Ignyta Inc, San Diego, CA 92121 USA
[4] Univ Milan, I-20122 Milan, Italy
基金
欧盟第七框架计划;
关键词
entrectinib; gene fusions; colorectal cancer; CAD-ALK; ALK; RESISTANCE; ROS1;
D O I
10.1038/bjc.2015.401
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Activated anaplastic lymphoma kinase (ALK) gene fusions are recurrent events in a small fraction of colorectal cancers (CRCs), although these events have not yet been exploited as in other malignancies. Methods: We detected ALK protein expression by immunohistochemistry and gene rearrangements by fluorescence in situ hybridisation in the ALKA-372-001 phase I study of the pan-Trk, ROS1, and ALK inhibitor entrectinib. One out of 487 CRCs showed ALK positivity with a peculiar pattern that prompted further characterisation by targeted sequencing using anchored multiplex PCR. Results: A novel ALK fusion with the carbamoyl-phosphate synthetase 2, aspartate transcarbamylase, and dihydroorotase (CAD) gene (CAD-ALK fusion gene) was identified. It resulted from inversion within chromosome 2 and the fusion of exons 1-35 of CAD with exons 20-29 of ALK. After failure of previous standard therapies, treatment of this patient with the ALK inhibitor entrectinib resulted in a durable objective tumour response. Conclusions: We describe the novel CAD-ALK rearrangement as an oncogene and provide the first evidence of its drugability as a new molecular target in CRC.
引用
收藏
页码:1730 / 1734
页数:5
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