Abstract
Molecular genetic testing of tumor material in colorectal cancer (CRC) is necessary for rational selection of drug therapy. Evaluation of RAS, BRAF, and HER2 genetic alterations and microsatellite instability (MSI) status is critical for patients with disseminated disease. Less common molecular markers with therapeutic implications include mutations in the POLE gene and rearrangements involving the tyrosine kinases NTRK1-3, RET and ALK. This review summarizes the incidence of these genetic alterations in CRC, their associations with clinical and morphological parameters, and their impact on prognosis.
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