Evidence map›Paper›PMID 41099850›Full record

ArticleVirchows Archiv : an international journal of pathology2025

Validation of Idylla MSI and BRAF genotype tests on archival colorectal cancer samples for retrospective Lynch syndrome detection.

Margarita Melnikova Jørgensen, Ida Elisabeth Gad Holm, Claus Lindbjerg Andersen, Jesper Bertram Bramsen, Parag Deepak Dabir

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Article in Virchows Archiv : an international journal of pathology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

5 authors.

Margarita Melnikova JørgensenInstitute of Pathology, Randers Regional Hospital, Randers, Denmark. mmjo@hst.aau.dk.ORCID http://orcid.org/0000-0001-8102-1855
Ida Elisabeth Gad HolmDepartment of Pathology, Aalborg University Hospital, Aalborg, Denmark.
Claus Lindbjerg AndersenDepartment of Clinical Medicine, Department of Molecular Medicine (MOMA), Aarhus University, Aarhus, Denmark.
Jesper Bertram BramsenDepartment of Clinical Medicine, Department of Molecular Medicine (MOMA), Aarhus University, Aarhus, Denmark.
Parag Deepak DabirInstitute of Pathology, Randers Regional Hospital, Randers, Denmark.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Microsatellite instability (MSI), detected via immunohistochemistry and/or polymerase chain reaction (PCR), is a hallmark for Lynch syndrome and a prognostic marker in colorectal cancer. While MSI status is assessed using immunohistochemistry on archival formalin-fixed paraffin-embedded (FFPE) tissue, interpretation can be challenging due to preanalytical variability, antigen decay, and observer subjectivity. PCR-based methods, like the Idylla system, offer a rapid automated alternative with minimal hands-on time and no requirement for specialized molecular facilities. We evaluated Idylla's performance on archival (≥ 10 years old) FFPE colorectal cancer resections by comparing BRAF and MSI analysis results with immunohistochemistry for DNA mismatch repair (MMR) proteins and previously performed PCR MSI (Pentaplex) and BRAF genotyping assays. MSI concordance was 94.3% (50/53) between Idylla and immunohistochemistry, and 98.1% (52/53) between Idylla and PCR. Two discordant samples were classified as MSI-high by Idylla and PCR, whereas immunohistochemistry showed normal MMR expression. Conversely, the third discordant sample was classified as microsatellite stable by Idylla and PCR, while immunohistochemistry indicated deficient MMR expression. For BRAF genotyping, concordance between Idylla and PCR was 92.7% (38/41). In two discordant samples, BRAF variants identified by PCR were not included in the Idylla panel, while the third discordant sample showed a pathogenic BRAF variant by Idylla not confirmed by PCR. This is the largest study evaluating Idylla on archival FFPE material. High concordance with traditional methods suggests that Idylla can be used as an alternative approach for Lynch syndrome screening, improving accessibility and reliability of MSI and BRAF testing in challenging archival specimens.

Indexed as

Archival formalin-fixed paraffin-embedded tissueBRAF genotypeDNA mismatch repair proteinsIdyllaLynch syndromeMicrosatellite status

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.