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Updated: Dec 26, 2025

Author Spotlight: Advancements in Molecular Biomarker Testing for Non-Squamous Non-Small Cell Lung Cancer
Published on: September 8, 2023
Rapid EGFR mutation testing in lung cancer tissue samples using a fully automated system and single-use cartridge
M Rabie Al-Turkmani1, Michael A Suriawinata1, Sophie J Deharvengt1
1Dartmouth-Hitchcock Medical Center and Geisel School of Medicine at Dartmouth. Lebanon, NH, USA.
Introduction:
Activating mutations in the tyrosine kinase domain of the epidermal growth factor receptor (EGFR) gene in non-small cell lung cancer (NSCLC) patients predicts response to EGFR tyrosine kinase inhibitors (TKIs). The Idylla™ system (Biocartis, Mechelen, Belgium) is a fully integrated, cartridge-based platform that provides automated sample processing and real-time PCR-based mutation detection in a single-use cartridge. This study evaluated the Idylla™ EGFR Mutation Assay cartridges against next-generation sequencing (NGS) using formalin fixed, paraffin embedded (FFPE) lung cancer tissue samples.
Methods:
Thirty-four FFPE lung adenocarcinoma tissue samples were tested on the Idylla™ system. 21 had at least one mutation in EGFR and 13 had no EGFR mutation as determined by NGS analysis using the Ion AmpliSeq 50-gene Cancer Hotspot Panel v2 (Thermo Fisher Scientific). One 10 μm FFPE tissue section was used for each Idylla™ test and all cases met the Idylla™ minimum tumor content requirement (≥10%).
Results:
Idylla™ results were in complete agreement with those obtained by NGS for EGFR mutations targeted by the Idylla™. NGS identified two additional EGFR mutations that are not targeted by the Idylla™ in two samples (E709V and V774M). No EGFR mutations were detected by the Idylla™ in samples determined by NGS as having wild-type EGFR.
Conclusion:
The fully automated Idylla™ system offers rapid and reliable testing for clinically actionable mutations in EGFR directly from FFPE tissue sections. Its simplicity and ease of use compared to other available molecular techniques make it suitable for routine clinical use in a variety of settings.
Insights
The Idylla™ EGFR Mutation Assay accurately detects epidermal growth factor receptor (EGFR) mutations in non-small cell lung cancer (NSCLC) tissue. This automated system provides reliable results comparable to next-generation sequencing (NGS) for clinical use.
Area of Science:
- Oncology
- Molecular Diagnostics
- Genetics
Background:
- Activating mutations in the epidermal growth factor receptor (EGFR) gene are key predictors of treatment response in non-small cell lung cancer (NSCLC).
- The Idylla™ system is a novel, automated platform for real-time PCR-based mutation detection.
- Evaluating novel diagnostic platforms is crucial for advancing personalized cancer therapy.
Purpose of the Study:
- To assess the performance of the Idylla™ EGFR Mutation Assay.
- To compare Idylla™ results with next-generation sequencing (NGS) for EGFR mutation detection.
- To determine the suitability of the Idylla™ system for clinical application in NSCLC.
Main Methods:
- Formalin-fixed, paraffin-embedded (FFPE) lung adenocarcinoma tissue samples (n=34) were analyzed.
- Samples were tested using the Idylla™ EGFR Mutation Assay.
- Results were compared against NGS analysis using the Ion AmpliSeq 50-gene Cancer Hotspot Panel v2.
Main Results:
- The Idylla™ system demonstrated complete agreement with NGS for targeted EGFR mutations.
- NGS identified two additional EGFR mutations (E709V, V774M) not covered by the Idylla™ assay.
- No EGFR mutations were detected by Idylla™ in samples identified as wild-type by NGS.
Conclusions:
- The Idylla™ system provides rapid and reliable detection of clinically actionable EGFR mutations from FFPE tissues.
- The assay's automation, simplicity, and ease of use support its routine clinical implementation.
- Idylla™ is a valuable tool for molecular testing in diverse clinical settings for NSCLC patients.
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