Efficient Lung Cancer Molecular Diagnostics by Combining Next Generation Sequencing with Reflex Idylla Genefusion Assay Testing.
Dingani NkosiGiby V GeorgeHuijie LiuMeghan BuldoMoises J VelezZoltán N OltvaiPublished in: Genes (2023)
Molecular diagnostics for lung cancer is a well-established standard of care, but how to use the available diagnostic tools for optimal and cost-effective patient care remains unresolved. Here, we show that DNA-only, small gene next-generation sequencing (sNGS) panels (<50 genes) combined with ultra-rapid reflex testing for common fusion transcripts using the Idylla Genefusion assay provide a cost-effective and sufficiently comprehensive testing modality for the majority of lung cancer cases. We also demonstrate the need for additional reflex testing capability on larger DNA and fusion panels for a small subset of lung cancers bearing rare single-nucleotide variants, indels and fusion transcripts and secondary, post-treatment resistance mutations. A similar testing workflow could be adopted for other solid tumor types for which extensive gene/fusion variant profiles are available both in the treatment-naïve and post-therapy settings.
Keyphrases
- copy number
- circulating tumor
- genome wide
- single molecule
- healthcare
- stem cells
- palliative care
- genome wide identification
- dna methylation
- high resolution
- cell free
- young adults
- mesenchymal stem cells
- mass spectrometry
- quality improvement
- pain management
- quantum dots
- health insurance
- replacement therapy
- genome wide analysis