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Updated: May 15, 2026

Oncogenic Gene Fusion Detection Using Anchored Multiplex Polymerase Chain Reaction Followed by Next Generation Sequencing
Published on: July 5, 2019
Multiplexed gene expression and fusion transcript analysis to detect ALK fusions in lung cancer
Maruja E Lira1, Tae Min Kim, Donghui Huang
1Pfizer Oncology, San Diego, California 92121, USA.
Abstract:
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.
Insights
A new NanoString assay effectively detects Anaplastic Lymphoma Kinase (ALK) gene fusions in non-small-cell lung cancer (NSCLC). This cost-effective method offers a high-throughput alternative for identifying patients who benefit from ALK inhibitors.
Area of Science:
- Oncology
- Molecular Diagnostics
- Genetics
Background:
- Anaplastic Lymphoma Kinase (ALK) gene fusions occur in ~5% of non-small-cell lung carcinomas (NSCLCs).
- Patients with ALK-positive NSCLC respond well to ALK inhibitors like crizotinib.
- Current ALK detection methods (FISH) are costly and have low throughput, limiting widespread screening.
Purpose of the Study:
- To develop and validate a novel, cost-effective, and high-throughput screening assay for ALK fusions in NSCLC.
- To explore transcript-based assays using NanoString's nCounter technology as an alternative to FISH.
Main Methods:
- A combination of two transcript-based assays was designed to detect ALK fusions.
- NanoString's nCounter technology was utilized for multiplexed gene expression and ALK fusion detection.
- The assay was validated on 66 archival NSCLC samples.
Main Results:
- The developed assay demonstrated high sensitivity, reproducibility, and quantitative scoring capabilities.
- It successfully detected low-abundant ALK fusion transcripts, even in samples with low tumor cell content.
- Results showed high concordance with established FISH and IHC methods.
Conclusions:
- The novel NanoString-based assay provides a sensitive, reproducible, and cost-effective screening alternative for ALK fusions in NSCLC.
- This assay is FFPE-compatible, easy to perform, and suitable for high-throughput screening.
- It facilitates broader identification of NSCLC patients eligible for ALK-targeted therapies.
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