Review Article
Predictive Biomarkers in Colorectal Cancer: From the Single Therapeutic Target to a Plethora of Options
Table 1
Summary of potential predictive biomarkers, available data, and current recommendations.
| Drug | Potential biomarkers | Data available | Current recommendations |
| 5-FU | TS expression | Inconsistent results | None | TP expression | Inconsistent results; high level potential indicator of poor prognosis | None | DPD expression | Not predictive; low levels associated with better prognosis | None |
| Irinotecan | UGT1A128/UGT1A16 polymorphisms | Not predictive; associated with severe toxicity | Patient screening for UGT1A128 and UGT1A16 (in Japan) polymorphisms |
| Oxaliplatin | ERCC1 | Inconsistent results | None |
| Cetuximab/panitumumab | KRAS mutation | Resistance to cetuximab/panitumumab | Patient screening for exon-2 KRAS mutations | BRAF V600E | Inconsistent results; poor prognosis | BRAF genotyping for stage IV CRC | PTEN loss | Not predictive | None | PIK3CA mutation | Not predictive | None |
| Bevacizumab | VEGF expression | Not predictive; contradictory data | None |
| ā | MSI-H | Resistance to chemotherapy; good prognosis | Determination of MSI status for all stage II CRC patients |
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5-FU: 5-fluorouracil; TS: thymidylate synthase; TP: thymidine phosphorylase; DPD: dihydropyrimidine dehydrogenase; UGT1A1: uridine diphosphate glucuronosyltransferase 1A1; ERCC1: excision repair cross-complementation group 1; VEGF: vascular endothelial growth factor; MSI-H: microsatellite instability-high.
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