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. 2013 Jul 26;4:2218. doi: 10.1038/ncomms3218

Table 1. Characteristics of the patients according to presence or absence of TERT promoter mutations (n=305).

Variable Overall series (n=305) TERT promoter mutated n=179 (59%) TERT promoter non-mutated n=126 (41%) P-value
Age
 >60 years* 187/305 (61%) 117 (65%) 70 (55%) 0.08
Gender
 Male* 242/305 (79%) 154 (86%) 88 (70%) 0.001
Aetiology
 HCV* 68/301 (26%) 49 (28%) 19 (15%) 0.03
 HBV* 67/303 (22%) 26 (15%) 41 (33%) <0.0001
 Alcohol* 118/300 (39%) 80 (46%) 38 (31%) 0.03
 Haemochromatosis* 19/299 (6%) 12 (7%) 7 (6%) 0.84
 Miscellaneous* 13/291 (5%) 7 (4%) 5 (4%) 0.74
 Unknown* 46/291 (16%) 22 (13%) 24 (20%) 0.14
Tumour size
 <5 cm* 127/303 (42%) 87 (49%) 40 (32%) 0.01
Tumour number
 Single* 212/304 (70%) 118 (66%) 94 (75%) 0.39
Vascular invasion
 Microvascular* 161/300 (54%) 91 (52%) 70 (56%) 0.7
 Macrovascular* 46/300 (15%) 28 (16%) 18 (14%) 0.94
Differentiation
 Edmonson I–II* 143/295 (48%) 83 (48%) 60 (49%) 0.70
 Edmonson III–IV* 152/295 (52%) 91 (52%) 61 (51%)  
Metavir score (non-tumour liver)
 F0–F1* 106/299 (35%) 58 (33%) 48 (38%) 0.21
 F2–F3* 83/299 (28%) 45 (26%) 38 (30%)  
 F4* 110/299 (37%) 71 (41%) 39 (32%)  
Preoperative AFP
 >20 ng ml−1* 123/274 (45%) 60 (38%) 63 (54%) 0.01
G1-G6 classification
 G1* 22/286 (8%) 9 (5%) 13 (11%) 0.12
 G2* 22/286 (8%) 13 (8%) 9 (8%)  
 G3* 53/286 (18%) 37 (22%) 16 (14%)  
 G4* 93/286 (32%) 49 (28%) 44 (38%)  
 G5* 62/286 (22%) 41 (24%) 21 (19%)  
 G6* 34/286 (12%) 22 (13%) 12 (10%)  
CTNNB1
 Mutated* 101/304 (33%) 75 (42%) 26 (21%) <0.0001
TP53
 Mutated* 60/302 (20%) 34 (19%) 26 (21%) 0.73
Events
 Median follow-up (months) 34/260 (17–56) 33 (16–54) 36 (22–58) 0.13
 Tumour-related death<5 years 92/260 (35%) 57 (37%) 35 (33%) 0.26
 Overall recurrence<5 years 138/260 (53%) 84 (55%) 54 (50%) 0.28

AFP, alpha-fetoprotein; HBV, hepatitis B; TERT, telomerase reverse-trancriptase.

*Expressed as number (%) and analysed using the χ2-test (group size of >5) with Yates’ continuity correction or Fisher’s exact test (group size of ≤5) except for multiple variable comparisons (χ2-test two sided). P-values were adjusted for multiple comparisons using Monte–Carlo resampling.

Expressed in months (median, 25th and 75th percentile) and analysed using the Kruskall–Wallis test.

Patients treated by surgical curative resection (R0) with available follow-up were included in the survival analysis (n=260), and survival analysis was performed using the log-rank test.