Table 1.
Training cohort | HCC (n = 804) | LC (n = 166) | FNH (n = 57) | LA (n = 15) | DN (n = 3) | ICC (n = 145) | Solid tumours (n = 129) |
---|---|---|---|---|---|---|---|
AFP RNAscope | 60.4% | 0.0% | 0.0% | 0.0% | 0.0% | 0.0% | 0.0% |
AFP IHC | 35.7% | 0.0% | 0.0% | 0.0% | 0.0% | 0.0% | 0.0% |
AFP ELISA | 39.2% | 1.8% | 1.8% | 0.0% | 0.0% | 0.0% | 0.0% |
GPC3 IHC | 80.0% | 15.7% | 0.0% | 0.0% | 33.3% | 0.7% | 0.8% |
HepPar-1 IHC | 84.1% | 83.1% | 96.5% | 93.3% | 100.0% | 2.1% | 0.0% |
Arg-1 IHC | 61.2% | 56.6% | 61.4% | 53.3% | 100.0% | 0.7% | 0.0% |
Validation cohort | HCC (n = 477) | LC (n = 25) | FNH (n = 11) | LA (n = 6) | DN (n = 5) | ICC (n = 84) | Solid tumours (n = 34) |
---|---|---|---|---|---|---|---|
AFP RNAscope | 66.5% | 4.0% | 0.0% | 0.0% | 0.0% | 0.0% | 0.0% |
AFP IHC | 33.8% | 4.0% | 0.0% | 0.0% | 0.0% | 0.0% | 0.0% |
AFP ELISA | 37.7% | 0.0% | 0.0% | 0.0% | 0.0% | 0.0% | 0.0% |
GPC3 IHC | 65.6% | 24.0% | 0.0% | 0.0% | 60.0% | 2.4% | 0.0% |
HepPar-1 IHC | 72.7% | 84.0% | 81.8% | 66.7% | 80.0% | 2.4% | 0.0% |
Arg-1 IHC | 69.4% | 80.0% | 72.7% | 83.3% | 100.0% | 0.0% | 0.0% |
Test cohort | HCC (n = 100) | LC (n = 8) | FNH (n = 18) | LA (n = 16) | DN (n = 20) | ICC (n = 32) | Metastatic carcinoma (n = 61) |
---|---|---|---|---|---|---|---|
AFP RNAscope | 45.0% | 0.0% | 0.0% | 0.0% | 0.0% | 0.0% | 0.0% |
AFP IHC | 28.0% | 12.5% | 0.0% | 0.0% | 5% | 0.0% | 0.0% |
AFP ELISA | 62.0% | 12.5% | 0.0% | 0.0% | 0.0% | 0.0% | 1.6% |
GPC3 IHC | 66.0% | 0.0% | 0.0% | 0.0% | 20% | 3.1% | 18.0% |
HepPar-1 IHC | 81.0% | 100% | 100% | 100% | 100% | 6.3% | 1.6% |
Arg-1 IHC | 61.0% | 100% | 100% | 100% | 100% | 0.0% | 0.0% |
HCC hepatocellular carcinoma, LC liver cirrhosis, FNH focal nodular hyperplasia, LA liver adenoma, DN dysplastic nodule, ICC intrahepatic cholangiocarcinoma, Solid tumours 15 types of non-HCC cancers (described in Fig. 1), Metastatic carcinoma 14 types of non-HCC cancers (described in Fig. 1), AFP ELISA AFP serum level >400 ng/ml was identified positive.