Abstract

Colorectal carcinoma (CRC) is one of the most commonly diagnosed cancers worldwide. The metastatic disease contributes to the high mortality rate reported for such tumors. Significant benefit on overall survival was brought about the introduction of monoclonal antibodies anti-EGFR and anti-VEGF used in combination with chemotherapy in metastatic CRC (mCRC). While anti-VEGF treatment does not require biomarker-based selection criteria, the potential efficacy of anti-EGFR antibodies is neglected to patients with activating mutations in KRAS and NRAS (RAS) genes that became a clinical routine. Recently, different molecular classification of CRC patients mostly based on omics approaches has been proposed. Although these might have implications for prognostic or therapy decisions, their immediate transfer to routine diagnostic/clinical settings is seriously challenging in terms of methodology, turnaround time, costs and mindset. As a consequence, to date, only few molecular biomarkers, such as RAS or BRAF, are routinely used in the standard clinical management of mCRC patients, but in the era of personalized therapy, we should be able to reach beyond the concept “one gene-one drug”. 

With the aim of responding to the clinical demand of RAS testing, many new rapid, sensitive and economic approaches have been implemented over the years, among them the NGS platforms. 

Keywords:  multigene panel