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. Author manuscript; available in PMC: 2024 Sep 1.
Published in final edited form as: J Hepatol. 2023 Sep 7;79(6):1469–1477. doi: 10.1016/j.jhep.2023.08.020

Table 1.

Baseline and waitlist characteristics of study population.

Patients (N = 285)
Median age at listing (years, IQR) 67.0 (63.0–71.0)
Sex (n, %)
 Men 214 (75.1)
 Women 71 (24.9)
Race (n, %)
 White 127 (44.6)
 Hispanic 67 (23.5)
 Asian/Pacific Islander 60 (21.1)
 African American 13 (4.6)
 Other 18 (6.3)
Etiology of liver disease (n, %)
 Hepatitis B or C 184 (64.6)
 NASH 44 (15.4)
 Alcohol Use 35 (12.3)
 Other 22 (7.7)
Tumor stage at diagnosis (n, %)
 Milan criteria 239 (83.9)
 UNOS downstaging 32 (11.2)
 All-comers 14 (4.9)
Median number of HCC viable lesions on explant (n, IQR) 1.0 (0–2.0)
Median size of largest tumor on explant (cm, IQR) 1.0 (0–1.8)
Median total viable tumor on explant (cm, IQR) 1.2 (0–3.0)
Locoregional therapy
 Ever received (n, %) 270 (94.7)
 Median number of treatments (n, IQR) 2 (1–3)
Types of locoregional therapy (n, %)
 TACE 189 (66.3)
 RFA 100 (35.1)
 Y90 73 (25.6)
Median MELD at listing (n, IQR) 11.0 (8.0–13.0)
Median MELD at transplant (n, IQR) 17.0 (13.0–21.0)
Median waitlist time to LT (years, IQR) 1.0 (0.6–1.4)
Median AFP at LT (ng/ml, IQR) 5.0 (3.0–12.1)
AFP ≥100 ng/ml at LT (n, %) 12 (4.2)
Median AFP-L3 at LT (%, IQR) 6.7 (0.5–13.2)
AFP-L3 ≥15% at LT (n, %) 57 (20.0)
Median DCP at LT (ng/ml, IQR) 1.0 (0.3–2.8)
DCP ≥7.5 ng/ml at LT (n, %) 40 (14.0)

AFP, alpha-fetoprotein; AFP-L3, AFP bound to Lens culinaris agglutinin; DCP, des-gamma-carboxyprothrombin; HCC, hepatocellular carcinoma; LT, liver transplant; MELD, model for end-stage liver disease; NASH, non-alcoholic steatohepatitis; RFA, radiofrequency ablation; TACE, transarterial chemoembolization; UNOS, United Network for Organ Sharing.