Multiplexed Gene Expression and Fusion Transcript Analysis to Detect ALK Fusions in Lung Cancer

被引:55
作者
Lira, Maruja E. [1 ]
Kim, Tae Min [2 ,3 ]
Huang, Donghui [1 ]
Deng, Shibing [1 ]
Koh, Youngil [3 ]
Jang, Bogun [4 ]
Go, Heounjeong [4 ]
Lee, Se-Hoon [2 ,3 ]
Chung, Doo Hyun [4 ]
Kim, Woo Ho [4 ]
Schoenmakers, Eric F. P. M. [1 ]
Choi, Yoon-La [5 ]
Park, Keunchil [6 ]
Ahn, Jin Seok [6 ]
Sun, Jong-Mu [6 ]
Ahn, Myung-Ju [6 ]
Kim, Dong-Wan [2 ,3 ]
Mao, Mao [1 ]
机构
[1] Pfizer Oncol, San Diego, CA 92121 USA
[2] Seoul Natl Univ, Coll Med, Canc Res Inst, Seoul, South Korea
[3] Seoul Natl Univ Hosp, Dept Internal Med, Seoul 110744, South Korea
[4] Seoul Natl Univ Hosp, Dept Pathol, Seoul 110744, South Korea
[5] Sungkyunkwan Univ, Sch Med, Samsung Med Ctr, Dept Pathol, Seoul, South Korea
[6] Sungkyunkwan Univ, Sch Med, Samsung Med Ctr, Dept Med, Seoul, South Korea
关键词
SMALL-CELL-LUNG; POLYMERASE CHAIN-REACTION; ANAPLASTIC LYMPHOMA; EML4-ALK; KINASE; INHIBITOR; IMMUNOHISTOCHEMISTRY; IDENTIFICATION; FEATURES;
D O I
10.1016/j.jmoldx.2012.08.006
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Anaplastic lymphoma kinase gene (ALK) fusions have been identified in approximately 5% of non-small-cell lung carcinomas (NSCLCs) and define a distinct subpopulation of patients with lung cancer who are highly responsive to ALK kinase inhibitors, such as crizotinib. Because of this profound therapeutic implication, the latest National Comprehensive Cancer Network Clinical Practice Guidelines in Oncology recommend upfront ALK screening for all patients with NSCLC. The Food and Drug Administration-approved companion diagnostic test (ie, fluorescence in situ hybridization) for identification of ALK-positive patients, however, is complex and has considerable limitations in terms of cost and throughput, making it difficult to screen many patients. To explore alternative screening modalities for detecting ALK fusions, we designed a combination of two transcript-based assays to detect for presence or absence of ALK fusions using NanoString's nCounter technology. By using this combined gene expression and ALK fusion detection strategy, we developed a multiplexed assay with a quantitative scoring modality that is highly sensitive, reproducible, and capable of detecting low-abundant ALK fusion transcripts, even in samples with a low tumor cell content. In 66 archival NSCLC samples, our results were highly concordant to prior results obtained by fluorescence in situ hybridization and IHC. Our assay offers a cost-effective, easy-to-perform, high-throughput, and FFPE-compatible screening alternative for detection of ALK fusions. (J Mol Diagn 2013, 15: 51-61; http://dx.doi.org/10.1016/j.jmoldx.2012.08.006)
引用
收藏
页码:51 / 61
页数:11
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