Incorporating traditional and emerging biomarkers in the clinical management of metastatic colorectal cancer: an update

Expert Rev Mol Diagn. 2020 Jul;20(7):653-664. doi: 10.1080/14737159.2020.1782194. Epub 2020 Jun 22.

Abstract

Introduction: Molecular profiling has led to significantly longer survival in metastatic colorectal cancer (mCRC) patients. Clinical guidelines recommend testing for KRAS/NRAS, BRAF and MSI status, and new biomarkers such as HER2 amplification and NTRK fusions have emerged more recently in refractory CRC, supported by overwhelming clinical relevance. These biomarkers can guide treatment management to improve clinical outcomes in these patients.

Areas covered: Preclinical and clinical data over the last decade were reviewed for known and novel biomarkers with clinical implications in refractory CRC. Molecular alterations are described for classic and novel biomarkers, and data for completed and ongoing studies with targeted and immunotherapies are presented.

Expert opinion: Use of targeted therapies based on biomarker testing in CRC has enabled impressive improvements in clinical outcomes in refractory patients. BRAF, MSI, NRAS and KRAS should be tested upfront in all patients given their indisputable therapeutic implications. Other molecular alterations such as HER2 and NTRK are emerging. Testing for these alterations may further improve outcomes for refractory CRC patients. Nonetheless, many key aspects remain to be defined including the optimal timing and technique for testing, the most adequate panel, and whether all patients should be tested for all alterations.

Keywords: BRAF; Biomarker; HER2; MSI; NTRK; colorectal cancer; ras refractory; relapse; targeted therapy.

Publication types

  • Review

MeSH terms

  • Adenocarcinoma / chemistry
  • Adenocarcinoma / genetics
  • Adenocarcinoma / secondary*
  • Adenocarcinoma / therapy
  • Biomarkers, Tumor / analysis*
  • Clinical Trials as Topic
  • Colorectal Neoplasms / chemistry*
  • Colorectal Neoplasms / genetics
  • Colorectal Neoplasms / therapy
  • DNA Mismatch Repair / genetics
  • DNA Modification Methylases / genetics
  • DNA Repair Enzymes / genetics
  • DNA, Neoplasm / blood
  • Genes, erbB-2
  • Genes, ras
  • Humans
  • Immune Checkpoint Inhibitors / therapeutic use
  • Liquid Biopsy
  • Membrane Glycoproteins / analysis
  • Membrane Glycoproteins / genetics
  • Microsatellite Instability
  • Molecular Targeted Therapy
  • Mutation
  • Neoplasm Proteins / analysis
  • Neoplasm Proteins / genetics
  • Oncogene Proteins, Fusion / analysis
  • Oncogene Proteins, Fusion / genetics
  • Proto-Oncogene Proteins B-raf / analysis
  • Proto-Oncogene Proteins B-raf / genetics
  • Receptor, trkA / analysis
  • Receptor, trkA / genetics
  • Receptor, trkB / analysis
  • Receptor, trkB / genetics
  • Receptor, trkC / analysis
  • Receptor, trkC / genetics
  • Tumor Suppressor Proteins / genetics

Substances

  • Biomarkers, Tumor
  • DNA, Neoplasm
  • Immune Checkpoint Inhibitors
  • Membrane Glycoproteins
  • NTRK1 protein, human
  • NTRK3 protein, human
  • Neoplasm Proteins
  • Oncogene Proteins, Fusion
  • Tumor Suppressor Proteins
  • DNA Modification Methylases
  • MGMT protein, human
  • Receptor, trkA
  • Receptor, trkB
  • Receptor, trkC
  • tropomyosin-related kinase-B, human
  • BRAF protein, human
  • Proto-Oncogene Proteins B-raf
  • DNA Repair Enzymes