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. 2016 Oct 25;6:35917. doi: 10.1038/srep35917

Table 1. Both HBV CP mutations and AKT were associated with poor HCC prognosis.

Variables All patients (n = 114) BHCC (n = 56) PHCC (n = 58) P value
Age (years)
 >50 43 (37.7) 19 (33.9) 24 (41.4) 0.445
 ≤50 71 (62.3) 37 (66.1) 34 (58.6)  
 Male, n (%) 97 (85.1) 46 (82.1) 51 (87.9) 0.380
Cirrhosis, n (%)
 Yes 83 (72.8) 35 (62.5) 48 (82.8) 0.020
 No 31 (27.2) 21 (37.5) 10 (17.2)  
Tumor size
 >5 cm, n (%) 73 (64.0) 30 (53.6) 43 (74.1) 0.048
 ≤5 cm, n (%) 41 (36.0) 26 (46.4) 15 (25.9)  
Tumor quantity, n (%)
 ≥3 11 (9.6) 1 (1.8) 10 (17.2) 0.001
  = 2 5 (4.4) 3 (5.3) 2 (3.5) 0.676
  = 1 98 (86.0) 52 (92.9) 46 (79.3) 0.057
Encapsulation, n (%)
 No 40 (35.1) 17 (30.4) 23 (39.7) 0.331
 Yes 74 (64.9) 39 (69.6) 35 (60.3)  
CHILD Classification, n (%)
 B 9 (7.9) 4 (7.1) 5 (8.6) 1.000
 A 105 (92.1) 52 (92.9) 53 (91.4)  
TNM classification, n (%)
 I 55 (48.2) 28 (50.0) 27 (46.6) 1.000
 II+III 59 (51.8) 28 (50.0) 31 (53.4)  
AFP (ng/ml), n (%)
 >400 47 (41.2) 22 (39.3) 25 (43.1) 0.707
 ≤400 67 (58.8) 34 (60.7) 33 (56.9)  
Ascites, n (%)
 Yes 11 (9.6) 5 (8.9) 6 (10.3) 0.525
 No 103 (90.4) 51 (91.1) 52 (89.7)  
Portal vein thrombosis, n (%)
 Positive 5 (4.4) 1 (1.8) 4 (6.9) 0.364
 Negative 109 (95.6) 55 (98.2) 54 (93.1)  
ALT (U/L), n (%)
 >ULN 70 (61.4) 34 (60.7) 36 (62.1) 0.711
 ≤ULN 44 (38.6) 22 (39.3) 22 (37.9)  
AST (U/L), n (%)
 >ULN 41 (36.0) 13 (23.2) 28 (48.3) 0.006
 ≤ULN 73 (64.0) 43 (76.8) 30 (51.7)  
Albumin (g/L), n (%)
 ≥40 80 (70.2) 45(80.4) 35 (60.3) 0.025
 <40 34 (29.8) 11 (19.6) 23 (39.7)  
Bilirubin (μmol/L), n (%)
 ≥23.9 13 (11.4) 6 (10.7) 7 (12.1) 1.000
 <23.9 101 (88.6) 50 (89.3) 51 (87.9)  
Prothrombin time (s), n (%)
 ≥12 12 (10.5) 5 (8.9) 7 (12.1) 1.000
 <12 102 (89.5) 51 (91.1) 51 (87.9)  
PLT (10E9/L), n (%)
 <170 41 (36.0) 20 (35.7) 21 (36.2) 1.000
 ≥170 73 (64.0) 36 (64.3) 37 (63.8)  
Alcohol use, n (%)
 Yes 41 (36.0) 19 (33.9) 22 (37.9) 0.699
 No 73 (60.0) 37 (66.1) 36 (62.1)  
HBV DNA (copies/ml), n (%)
 >6.0E+06 33 (28.9) 10 (19.6) 23 (37.9) 0.021
 ≤6.0E+06 81 (71.1) 46 (80.4) 35 (62.1)  
HBsAg (IU/ml), n (%)
 ≤500 60 (52.6) 36 (64.3) 24 (41.4) 0.025
 >500 54 (47.4) 20 (35.7) 34 (58.6)  
HBV genotypes, n (%)
 B 66 (57.9) 32 (57.1) 34 (58.6) 1.000
 C 48 (42.1) 24 (42.9) 24 (41.4)  
CP status, n (%)
 WT 22 (19.3) 16 (28.6) 6 (10.3) 0.018
 TA 24 (21.1) 14 (25.0) 10 (17.2) 0.362
 TACO 68 (59.6) 26 (46.4) 42 (72.4) 0.007
pAKT1 expression, n (%)
 High 50 (43.9) 18 (32.1) 32 (55.2) 0.015
 Low 64 (56.1) 38 (67.9) 26 (44.8)  

Samples in the PHCC group expressed significantly higher levels of pAKT than samples in the BHCC group (55.2% vs. 32.1%; P = 0.015). Moreover, TACO mutations were more common in the PHCC group than in the BHCC group (72.4% vs. 46.4%; P = 0.007). The data were analysed using SPSS, version 15, and the results are expressed as a percentage. Categorical variables were compared with a chi-square test or Fisher’s exact test. P values < 0.05 were considered to indicate significant differences. PHCC, HCC patients with a poor prognosis (less than 5-year survival); BHCC, HCC patients with a better prognosis (more than 5-year survival); ALT, alanine transferase; AST, aspartate transferase; AFP, alpha fetal protein; PLT, platelet; ULN, upper limit of normal; LLN, lower limit of normal.