©The Author(s) 2015.
World J Hepatol. Jun 28, 2015; 7(12): 1632-1651
Published online Jun 28, 2015. doi: 10.4254/wjh.v7.i12.1632
Published online Jun 28, 2015. doi: 10.4254/wjh.v7.i12.1632
Table 2 Currently used and investigational serum tumour markers[101]
| Markers | Character | Cut-off level | Sensitivity | Specificity | Comments |
| AFP | Oncofoetal glycoprotein | 10-16 ng/dL | 60%-80% | 70%-90% | Poor marker alone |
| 20 ng/dL | 39%-66% | 76%-97% | |||
| AFP-L3 | AFP variant (subtype) | 10% | 39.9% | 93.4% | Useful in combination |
| 15% | 36.1%-96% | 92%-99.5% | with other markers | ||
| GP73 | Golgi-specific membrane protein | 10 relative units | 69% | 86% | Promising marker |
| GPC3 | Oncofoetal glycoprotein | 2 ng/dL | 51% | 90% | Limited utility as a marker |
| DCP | Abnormal prothrombin | 40 mAU/mL | 48%-62% | 81%-98% | Useful in combination |
| HS-GGT | Abnormal prothrombin | 5.5 IU/mL | 43.8%-74% | Not available | Non specific |
| AFU | Lysosomal enzyme | 870 nmol/mL per hour | 82% | 71% | Lower specificity and poor marker |
- Citation: Attwa MH, El-Etreby SA. Guide for diagnosis and treatment of hepatocellular carcinoma. World J Hepatol 2015; 7(12): 1632-1651
- URL: https://www.wjgnet.com/1948-5182/full/v7/i12/1632.htm
- DOI: https://dx.doi.org/10.4254/wjh.v7.i12.1632