Biocartis: Two Performance Studies on Idylla(TM) MSI Biomarkers Selected for Publication at ASCO Conference

 

Biocartis Group NV (the 'Company' or 'Biocartis'), an innovative molecular diagnostics company (Euronext Brussels: BCART), today announces that two studies conducted in cooperation with the Flemish Institute for Biotechnology (VIB) regarding the performance of its exclusively licensed novel set of biomarkers for microsatellite instability (MSI) that are included in the Idylla(TM) MSI Assay (the 'MSI Biomarkers'), have been selected for publication at the ASCO (American Society of Clinical Oncology) Annual Meeting, taking place between 1-5 June 2018 in Chicago, US. The first study uses the prototype Idylla(TM) MSI Assay in finalized design and shows superior performance of the MSI test compared to reference methods. The second study underlines the potential of Biocartis' MSI Biomarkers[1] to be used as a companion diagnostic to predict immunotherapy outcome in MSI-High[2] endometrial and colorectal tumors.

MSI is the result of inactivation of the body's so-called DNA mismatch repair (MMR) system. Consequently, errors that normally spontaneously occur during DNA replication are no longer corrected, contributing to tumor growth and evolution. Detection of MSI is currently recommended for all patients with colorectal cancer (CRC). Current MSI testing methods rely on manual, lengthy and complex procedures involving amongst others obtaining and testing of a second reference sample. The fully automated Idylla(TM) MSI Assay is expected to overcome these drawbacks, providing results within 150 minutes from just one slice of FFPE[3] tumor tissue, without requiring a reference sample.


The first study[4] used the prototype Idylla(TM) MSI cartridges in a finalized design, containing a new set of seven MSI Biomarkers, consisting of short homopolymers located in the ACVR2A, BTBD7, DIDO1, MRE11, RYR3, SEC31A and SULF2 genes, to test 348 FFPE colorectal cancer samples[5] on their MSI status (i.e. MSI-High2 or Microsatellite stable). A concordance analysis with a reference methodology[6] showed an overall agreement of 96.1%. Of the discordant results, fourteen cases were classified as MSI-High by Idylla(TM) but Microsatellite stable (11) or invalid (3) by the reference method. Based on these results, the study concluded that the prototype Idylla(TM) MSI Assay is capable of faster detection with excellent sensitivity and significantly less invalid results compared to reference molecular testing for MSI.


The second study[7], based on 33 samples, demonstrated that the MSI Biomarkers reliably identified MSI-High status in endometrial and colorectal cancer[8] and that MSI-High is correlated to the total insertion-deletion (indel) load of the tumor. These indel mutations increase tumor responsiveness to checkpoint blockade immunotherapies, which is a type of immunotherapy where the power of a patient's immune system is harnessed to attack tumors. Checkpoint blockade immunotherapies were recently US FDA approved for the treatment of MSI-High tumors. As such, the study concluded that the MSI Biomarkers could potentially be used to predict immunotherapy outcome in MSI-High tumors.


Prof. Diether Lambrechts, Director of the VIB - KU Leuven Center for Cancer Biology, commented: "These studies clearly show the high clinical value of the MSI Biomarkers, first identified in our lab and now meticulously further selected to a set of seven biomarkers by Biocartis that are combined with the advantages of the fully automated Idylla(TM) system. The seven biomarkers show a remarkable association with both tumor mutational burden and total indel load. This provides us with a potential novel and easy-to-implement tool to predict tumor response to checkpoint blockade immunotherapy".


Herman Verrelst, CEO Biocartis, reacted: "The selected ASCO studies once more demonstrate the innovative nature of the Idylla(TM) MSI Assay that we have under development. In our view, the unique features of this test are of great value to the pharmaceutical industry that needs rapid, reliable and easy MSI testing for a broad rollout of their immune-oncology treatments. Together we could enable more patients with MSI-High tumors to benefit from these promising immunotherapy treatments."
The launch of Biocartis' fully automated Idylla(TM) MSI Assay (RUO[9]) is planned for H2 2018.

 

Note

Biocartis (Euronext Brussels: BCART) is an innovative molecular diagnostics (MDx) company providing next generation diagnostic solutions aimed at improving clinical practice for the benefit of patients, clinicians, payers and industry. Biocartis' proprietary MDx Idylla(TM) platform is a fully automated sample-to-result, real-time PCR (Polymerase Chain Reaction) system that offers accurate, highly reliable molecular information from virtually any biological sample in virtually any setting. Biocartis launched the Idylla(TM) platform in September 2014. Biocartis is developing and marketing a rapidly expanding test menu addressing key unmet clinical needs in oncology and infectious diseases. These areas represent respectively the fastest growing and largest segments of the MDx market worldwide. Today, Biocartis offers fourteen oncology tests and two infectious disease tests in Europe. More information: www.biocartis.com. Follow us on Twitter: @Biocartis_.

 

 

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