Integrating the Idylla™ System Alongside a Real-Time Polymerase Chain Reaction and Next-Generation Sequencing for Investigating Gene Fusions in Pleural Effusions from Non-Small-Cell Lung Cancer Patients: A Pilot Study.
Stefania ScarpinoAlvaro LeoneDino GalafateFrancesco PepeUmberto MalapelleSandra VillaniEnrico GiarnieriGiulio MauriziClaudia De VitisRita ManciniMassimiliano ManciniArianna Di NapoliAndrea VecchioneEmanuela PilozziPublished in: International journal of molecular sciences (2024)
Malignant pleural effusion (MPE) from patients with advanced non-small-cell lung cancer (NSCLC) has been proven valuable for molecular analysis; however, simultaneous detection of driver fusions in MPE is still challenging. In this study, we investigated the Idylla™ GeneFusion Panel, a stand-alone test in tissue samples, in the evaluation of ALK , ROS1 , RET and MET ex14 skipping mutations in MPE and compared its performance with routine reference methods (Real-time-based and Next-generation Sequencing-NGS). The inclusion criteria for sample selection were as follows: advanced NSCLC harboring ALK , ROS1 , RET fusions or MET exon-skipping alterations and the availability of MPE collected at diagnosis or disease progression. Molecular alterations have been investigated on tissue by fluorescence in situ hybridization (FISH) or Real-time PCR or NGS. For molecular profiling with the Idylla™ GeneFusion, 200 µL of MPE supernatants combined with 50 µL of RNA Later solution were loaded into the Idylla™ cartridge without cfRNA extraction. The Idylla™ GeneFusion Assay performed on MPEs was able to confirm molecular profile, previously diagnosed with conventional methods, in all cases. Our data confirm that MPE are suitable material for investigating fusion alterations. The Idylla™ GeneFusion, although indicated for investigation of tissue samples, offers the possibility of performing a molecular characterization of supernatants without undertaking the entire cfRNA extraction procedure providing a rapid and reliable strategy for the detection of actionable genetic alterations.
Keyphrases
- advanced non small cell lung cancer
- real time pcr
- epidermal growth factor receptor
- copy number
- loop mediated isothermal amplification
- tyrosine kinase
- single molecule
- small cell lung cancer
- single cell
- cell death
- genome wide
- dna damage
- drug delivery
- electronic health record
- minimally invasive
- gene expression
- high throughput
- mesenchymal stem cells
- stem cells
- big data
- clinical practice
- circulating tumor
- sensitive detection
- mass spectrometry
- quantum dots
- transcription factor
- data analysis
- cell free