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. 2023 May 25;13(1):89–98. doi: 10.1159/000531182

Table 1.

Baseline clinical characteristics

All patients (n = 208) Thyroid AE (n = 41) No thyroid AE (n = 167) p value
Age, median (IQR), years 61.0 (54.3–68.0) 62.0 (54.0–67.5) 61.0 (54.0–68.0) 0.822
Male sex, n (%) 179 (86.1) 33 (80.5) 146 (87.4) 0.251
ECOG performance status, n (%)
 0 97 (46.6) 19 (46.3) 78 (46.7) 0.967
 1 111 (53.4) 22 (53.7) 89 (53.3)
Child-Pugh classification, n (%)
 A 169 (81.3) 35 (85.4) 134 (80.2) 0.451
 B 39 (18.8) 6 (14.6) 33 (19.8)
Barcelona clinical liver cancer stage, n (%)
 B 38 (18.3) 9 (22.0) 29 (17.4) 0.496
 C 170 (81.7) 32 (78.0) 138 (82.6)
AFP ≥400 ng/mL, n (%) 72 (34.6) 9 (22.0) 63 (37.7) 0.057
NLR, median (IQR) 2.6 (1.7–4.2) 2.1 (1.6–3.5) 2.8 (1.8–4.2) 0.040
Presence of MVI, n (%) 84 (40.4) 17 (41.5) 67 (40.1) 0.875
Presence of extrahepatic spread, n (%) 127 (61.1) 23 (56.1) 104 (62.3) 0.467
Etiology of HCC, n (%)
 Hepatitis B 143 (68.8) 28 (68.3) 115 (68.9) 0.663
 Hepatitis C 13 (6.3) 1 (2.4) 12 (7.2)
 Alcohol 25 (12.0) 6 (14.6) 19 (11.4)
 Other or unknown 27 (13.0) 6 (14.6) 21 (12.6)
Prior local therapy for HCC, n (%) 145 (69.7) 32 (78.0) 113 (67.7) 0.195

Significant p values in bold.

AE, adverse event; IQR, interquartile range; ECOG, Eastern Cooperative Oncology Group; HCC, hepatocellular carcinoma; AFP, alpha-fetoprotein; MVI, macrovascular invasion.