Vår Kref GeneTest :

* CancerPrecision®


There is no ‘one-size-fits-all’ in cancer medicine, as every patient and every tumor is unique.

Thus, it is vital to understand the disease history and each tumor in the best possible way. As every cancer results from genetic changes in the tumor genome (somatic mutations), cancer is considered a genetic disease. On top of that, in every fifth patient, cancer predisposition is inherited. Identifying inherited variants and genetic changes within the tumor provides valuable information for choosing the most efficient treatment for each patient. We at CeGaT have fully committed ourselves to provide the best possible diagnostic approach. With our long-term experience in genetic testing, we have brought our tumor diagnostic tools to the next level. We aim to identify every possible therapeutically relevant change in the tumor. We have optimized target enrichment and complement by sequencing on NovaSeq6000, the latest and most reliable sequencing technology. With our interdisciplinary team of experts, we uncover and interpret genetic variants responsible for tumor growth, drug resistance, treatment efficacy, and highlight potential pharmaceutical toxicity.

By using next-generation sequencing (NGS) technology, we analyze a panel of 766 tumor-associated genes and selected therapy relevant fusions in 31 genes. Variations in these genes are known to have a significant impact on tumor pathogenesis, progression and metastasis. Concerning immunotherapies we determine tumor mutational burden (TMB) and microsatellite instability (MSI). Targeted RNA-based fusion analysis allows the detection of fusion transcripts with de-novo and known partners in 103 genes. The generated data is summarized in a comprehensive report supporting the treating physician in finding efficient treatment for each patient.

Our somatic tumor panel CancerPrecision® is the first choice genetic diagnostics for cancer patients.

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* Registered product of CeGaT.

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