Table 3.
Biomarker | Results | Clinical Application/Future Direction |
---|---|---|
T-cell/macrophage ratio [49] | High T-cell/macrophage ratio in TME after neoadjuvant chemotherapy, longer survival | Selection of patients for immune checkpoint inhibitors after neoadjuvant chemotherapy |
miR-31-3p [50,51] | High expression in KRAS WT treated with anti-EGFR therapy, inferior outcome | Predictive biomarker for the patients with KRAS WT receiving anti-EGFR treatment |
BRAF [55] | Worse prognostic factor in the first year after hepatectomy for CLM than margin status | Selection of patients for additional resection in cases with recurrence after resection for CLM |
TP53, and SMAD4 [56] | Coexisting mutations in RAS, TP53, and SMAD4, worse survival compared with single or double mutations | Accurate prediction of prognosis in patients with CLM |
R-spondin [57] | Association with vascular endothelial growth factor-dependent angiogenesis | Selection of patients who gain mostly from the addition of bevacizumab to chemotherapy |
CMS [58,59,60] | CMS2 and CMS3 preferred bevacizumab over other CMS groups | Planning perioperative systemic treatment for patients with CLM |
Abbreviations: TME: Tumor microenvironment; CMS: consensus molecular subtypes.