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Multi-Center Evaluation of the Fully Automated PCR-Based Idylla™ KRAS Mutation Assay for Rapid KRAS Mutation Status
Jérôme Solassol1, Julie Vendrell1, Bruno Märkl2
1Laboratory of Biopathology, Institut du Cancer de Montpellier, Montpellier, France.
Abstract:
Since the advent of monoclonal antibodies against epidermal growth factor receptor (EGFR) in colorectal cancer therapy, the determination of RAS mutational status is needed for therapeutic decision-making. Most prevalent in colorectal cancer are KRAS exon 2 mutations (40% prevalence); lower prevalence is observed for KRAS exon 3 and 4 mutations (6%) and NRAS exon 2, 3, and 4 mutations (5%). The Idylla™ KRAS Mutation Test on the molecular diagnostics Idylla™ platform is a simple (<2 minutes hands-on time), highly reliable, and rapid (approximately 2 hours turnaround time) in vitro diagnostic sample-to-result solution. This test enables qualitative detection of 21 mutations in codons 12, 13, 59, 61, 117, and 146 of the KRAS oncogene being clinically relevant according to the latest clinical guidelines. Here, the performance of the Idylla™ KRAS Mutation Assay, for Research Use Only, was assessed on archived formalin-fixed paraffin-embedded (FFPE) tissue sections by comparing its results with the results previously obtained by routine reference approaches for KRAS genotyping. In case of discordance, samples were assessed further by additional methods. Among the 374 colorectal cancer FFPE samples tested, the overall concordance between the Idylla™ KRAS Mutation Assay and the confirmed reference routine test results was found to be 98.9%. The Idylla™ KRAS Mutation Assay enabled detection of 5 additional KRAS-mutated samples not detected previously with reference methods. As conclusion the Idylla™ KRAS Mutation Test can be applied as routine tool in any clinical setting, without needing molecular infrastructure or expertise, to guide the personalized treatment of colorectal cancer patients.
Insights
The Idylla™ KRAS Mutation Test accurately identifies RAS mutations in colorectal cancer patients, aiding personalized treatment decisions. This rapid molecular diagnostic test demonstrates high concordance with reference methods.
Area of Science:
- Oncology
- Molecular Diagnostics
- Genetics
Background:
- Epidermal growth factor receptor (EGFR) targeted therapy in colorectal cancer (CRC) necessitates RAS mutational status determination.
- KRAS mutations are prevalent in CRC, with specific mutations in KRAS and NRAS codons guiding treatment decisions.
Purpose of the Study:
- To evaluate the performance of the Idylla™ KRAS Mutation Assay for detecting clinically relevant KRAS mutations in colorectal cancer formalin-fixed paraffin-embedded (FFPE) tissues.
- To assess the concordance of the Idylla™ test with established KRAS genotyping reference methods.
Main Methods:
- The Idylla™ KRAS Mutation Assay was used on 374 CRC FFPE samples.
- Results were compared against routine reference KRAS genotyping methods.
- Discordant results were further investigated using additional analytical methods.
Main Results:
- The Idylla™ KRAS Mutation Assay showed 98.9% overall concordance with confirmed reference test results.
- The assay identified 5 additional KRAS-mutated samples missed by reference methods.
- The test demonstrated high reliability and a rapid turnaround time (approx. 2 hours).
Conclusions:
- The Idylla™ KRAS Mutation Test is a reliable and rapid tool for qualitative detection of 21 clinically relevant KRAS mutations.
- It can be implemented in routine clinical settings without specialized molecular infrastructure or expertise.
- The assay supports personalized treatment strategies for colorectal cancer patients based on RAS mutational status.
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