Biocartis Group NV: Biocartis launches CE-marked IVD test for lung cancer


PRESS RELEASE: 13 June 2017, 07:00 CEST

Biocartis launches CE-marked IVD test for lung cancer
Idylla(TM) EGFR Mutation Test is the only on market fully automated CE-IVD test detecting all relevant EGFR mutations according to international guidelines

Mechelen, Belgium, 13 June 2017 - Biocartis Group NV (`Biocartis` or the `Company`), an innovative molecular diagnostics company (Euronext Brussels: BCART), today announced the CE-marking of the Idylla(TM) EGFR Mutation Test, as such achieving an important milestone in Biocartis` lung cancer menu. The test is the only on market fully automated CE-IVD test that detects all relevant EGFR mutations according to international guidelines[1]. A comparison study[2] of the Idylla(TM) EGFR Mutation Test, of which an abstract was published at the 2017 ASCO Annual Meeting[3], compared the test with a commonly used EGFR pyrosequencing-based test[4]. This study concluded that the Idylla(TM) EGFR Mutation Test produced the results faster and easier, based on only one slice of tumor tissue[5]. As such this test has the potential to expand EGFR testing to more pathology laboratories in a reliable and fast manner.

Lung cancer is the most common cancer worldwide, contributing for 13% of all cancer types[6] and in total 85% of lung cancers are non-small cell lung cancers (NSCLC)[7]. The prevalence of EGFR mutations in NSCLC is 10-15% in Western and up to 50% in Asian patients[8]. Today, EGFR mutation testing is recommended in all patients with advanced NSCLC of a non-squamous subtype[9]. Current molecular testing of lung cancer samples however is still a very complex process. It can take up to several weeks[10] before results are generated, mainly because obtaining high quality tissue samples is difficult. Samples are often small, with a limited amount of available lung tumour tissue, leading to failure of test results in a significant number of cases. Moreover, many laboratories do not have the necessary infrastructure to perform complex molecular tests, resulting in laboratories sending out their samples to other testing facilities, causing long waiting times.

The Idylla(TM) EGFR Mutation Test, performed on Biocartis` Idylla(TM) platform, is designed to improve today`s complex EGFR testing workflows. The test allows the detection of 51 EGFR mutations directly from only one slice of FFPE tissue, in contrast with traditional EGFR testing methods that often require up to six or more tumor slices. The test delivers results in approx. 2.5 hours with less than 2 minutes hands-on time. The clinical performance evaluation comparing the Idylla(TM) EGFR Mutation Test with a Polymerase Chain Reaction (PCR) based reference method showed an overall agreement of 96%[11] for mutations in the EGFR oncogene. A comparison study2, of which an abstract was published at the 2017 ASCO Annual Meeting, compared the EGFR Mutation Test on the Idylla(TM) platform to a pyrosequencing method commonly used in clinical practice. This study concluded that the Idylla(TM) EGFR Mutation Test produced the results faster (sample-to-result time was about 180 minutes with about two minutes of hands-on time) than pyrosequencing (sample to result time about 12 hours) and easier.