Abstract

Universal testing of microsatellite instability (MSI) is recommended for colorectal cancer (CRC) and endometrial cancer (EC) to screen for Lynch syndrome and to aid in assessing prognosis and optimal treatment. We compared the performance of Idylla MSI test to immunohistochemistry (IHC) of mismatch repair (MMR) proteins in consecutive series of 100 CRC and 108 EC samples, as well as in retrospective series of 28 CRC and 33 EC specimens with known deficient MMR protein expression. The concordance between the Idylla test and IHC was 100% in all CRC samples (n=128) but lower in EC samples (87.2%; n=141). In the EC samples, sensitivity of Idylla test was 72.7% and specificity 100%. EC MSI/dMMR agreement was 85.4% for MLH1, 87.5% for MSH2, and only 35.3% for MSH6. When we analyzed 14 EC samples that were discrepant, i.e., dMMR using IHC and microsatellite stable using Idylla, with microsatellite markers BAT25 and BAT26, we found four cases to be replication error (RER) positive. All RER positive cases were deficient for MSH6 protein expression. We also re-analyzed EC samples with variable tumor cellularity to determine the limit of detection of the Idylla test and found that a 30% or higher tumor cellularity is required. We conclude that Idylla MSI test offers a sensitive and specific method for CRC diagnostics but is less sensitive in EC samples especially in the case of MSH6 deficiency.

Highlights

  • Microsatellites are short repetitive DNA sequences that are prone to replication errors (RER)

  • We collected a consecutive series of 108 endometrial cancers (EC) samples (EC Set I) from patients operated at Helsinki University Hospital (HUH) between February 2018 and March 2020, which were analyzed in blinded manner using Idylla Microsatellite instability (MSI) test

  • colorectal cancer (CRC) tumor cell percentages estimated for the Idylla analysis varied between 20 and 90%, and none of the Idylla test results were invalid

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Summary

Introduction

Microsatellites are short repetitive DNA sequences that are prone to replication errors (RER). Microsatellite instability (MSI) is caused by deficient mismatch repair (dMMR) system, leading to hypermutation phenomenon and cancer susceptibility [1, 2]. Applied Tumor Genomics Research Program, Research Programs Unit, University of Helsinki, Helsinki, Finland Universal testing of MSI is recommended for CRC and EC patients to screen for LS and to aid in assessing prognosis and determining optimal treatment and follow-up [6,7,8]

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