Cancer Genomics for Clinicians

Identifying the right treatment for your cancer patients – the benefits of comprehensive molecular profiling

Every patient is unique, reacting in different ways to the therapy they receive.

Every tumor is unique, exhibiting its own set of genome and epigenome alterations.

In the context of cancer treatment, this individuality represents a particular challenge due to the heterogeneity of tumors. This heterogeneity can be seen at all levels of molecular aberrations, including the genome (DNA), transcriptome (RNA) and proteome (proteins). These alterations can represent important markers influencing treatment decisions, with several genomic biomarkers already being used as part of standard-of-care treatment regimens (e.g. EGFR mutations in lung cancer). A number of other aberrations have been shown to represent valuable markers in pre-clinical and clinical studies, but they are not yet part of routine clinical procedure. It is clear, however, that basing diagnosis on a restricted range of mutations runs the risk of overlooking a large amount of clinically relevant information. Due to rapid progress in sequencing technologies and analysis methods, comprehensive molecular profiling is now an affordable undertaking.

The approach of conducting a comprehensive molecular analysis of a patient and their tumor generates information that has a higher likelihood of significantly improving treatment strategies and outcomes. This analysis includes predictive biomarkers (e.g. EGFR mutations) for targeted therapy, markers associated with immune-therapy or chemotherapy outcomes, prognostic (e.g. TP53 mutations) and diagnostic biomarkers (e.g. EWSR1 fusions) as well as predisposing mutations (e.g. BRCA mutations).

What we provide

The unique personalized analysis offered by Alacris Theranostics

Alacris Theranostics’ cancer genomics services for clinicians provide a highly comprehensive tumor characterization based on deep sequencing of the cancer transcriptome and genome, as well as of the patient genome.

Our Comprehensive Molecular Tumor Analysis (CMTA) generates a detailed molecular profile of each individual tumor.

The CMTA is based on our cutting-edge powerful NGS analysis pipeline which integrates Whole-Exome Sequencing (WES), shallow or full Whole-Genome Sequencing (WGS) and RNA Sequencing (RNAseq). We routinely employ both WES and shallow WGS of tumor and normal control samples to call genomic aberrations, such as mutations, amplification, deletions or gene fusions. We also employ RNA sequencing to identify alterations in signaling pathways, gene over- or underexpression, and to support the identification of gene fusions. These results are reviewed by experts in bioinformatics, molecular biology, and oncology.

Complexity made simple

The CTMA delivers one clear and concise fully annotated report to the clinician containing the following multi-level molecular information:

  • Mutations in genes and clinically-relevant regions of the genome
  • Whole genome chromosome alterations (digital karyotype)
  • Regions with loss of heterozygosity (LOH)
  • Gene fusions
  • Gene amplification and associated expression
  • Full analysis of altered gene expression in the tumor
  • Analysis of the tumor microenvironment and immune infiltration
  • Biological annotation of the findings
  • Annotation for approved targeted therapies and clinical trials
  • Landscape of the tumor type and microenvironment

Since the CMTA results will have different impacts on clinical practice depending on the patient, tumor type and stage, a discussion of the hopes and promises of personalized oncology as well as a preselection of patients who are most likely to benefit from comprehensive molecular diagnostics is key to successfully harnessing biomedical research for clinical routine.

The CMTA supplies clinicians with the necessary information to support their treatment decisions. The high quality data interpretation and expert insight provided will facilitate identification of the best treatment option.

We are always available to answer any questions that might arise. Please contact us via or by using the contact form below.

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