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. 2023 Mar 31;12(10):11513–11524. doi: 10.1002/cam4.5880

TABLE 1.

Baseline characteristics of study patients.

Characteristics T‐L‐P group (n = 54) T‐L group (n = 45) TACE alone (n = 40) p‐value
Age (year) 0.142
Median ± SD 57.0 ± 9.9 60.8 ± 9.4 58.6 ± 9.4
Range 35–79 43–80 40–74
Sex 0.684
Male 49(90.7) 43 (95.6) 38 (95.0)
Female 5(9.3) 2 (4.4) 2(5.0)
Chronic hepatitis B 1.000
Yes 52 (96.3) 43 (95.6) 39(97.5)
No 2 (3.7) 2 (4.4) 1(2.5)
Hepatic cirrhosis 0.708
Yes 20 (37.0) 13 (28.9) 14(35.0)
No 34 (63.0) 32 (71.1) 26(65.0)
AFP (ng/mL) 0.455
≥400 14 (25.9) 7 (15.6) 8(20.0)
<400 40 (74.1) 38 (84.4) 32(80.0)
DCP (mAU/mL) 0.482
≥2050 12 (22.2) 9 (20.0) 5(12.5)
<2050 42 (77.8) 36 (80.0) 35(87.5)
MVI 0.465
MVI (−) 27 (50.0) 28 (62.2) 23(57.5)
MVI (+) 27 (50.0) 17 (37.8) 17(42.5)
Tumor size (cm) 0.134
≥2 28 (51.9) 21 (46.7) 15(37.5)
<2 26 (48.1) 41 (53.3) 25(62.5)
Recurrence interval (year) 0.528
<2 44 (81.5) 33 (73.3) 33(82.5)
≥2 10 (18.5) 12 (26.7) 7(17.5)
TB (μmol/L) 0.129
Median ± SD 22.3 ± 14.2 18.2 ± 10.5 18.1 ± 8.8
Range 6.0–69.2 7.1–73.2 7.5–56.4
ALB (g/L) 0.378
Median ± SD 40.3 ± 6.4 41.3 ± 7.4 42.2 ± 5.6
Range 16.0–55.0 17.0–67.4 21.0–67.4
ALT (U/L) 0.401
Median ± SD 45.1 ± 24.5 38.7 ± 24.9 44.0 ± 23.9
Range 8.0–94.0 9.0–107.0 9.0–96.0
AST (U/L) 0.940
Median ± SD 45.5 ± 20.6 46.9 ± 28.4 47.0 ± 24.6
Range 11.0–86.0 14.0–130.0 10.0–121.0
PT (sec) 0.274
Median ± SD 12.0 ± 1.1 11.8 ± 1.0 11.7 ± 0.74
Range 10.2–15.1 10.4–14.3 10.6–13.7
ALBI grade 0.689
1 28 (51.9) 28 (62.2) 25 (62.5)
2 25 (46.3) 16 (35.6) 15 (37.5)
3 1 (1.9) 1 (2.2) 0 (0)
Child–Pugh 0.663
A (5–6) 49 (90.7) 42 (93.3) 35 (87.5)
B (7–8) 5 (9.3) 3 (6.7) 5 (12.5)
ECOG (performance status) 0.522
0 46 (85.2) 41 (91.1) 33 (82.5)
1 8 (14.8) 4 (8.9) 7(17.5)
HBV‐DNA (IU/mL) 0.302
≥50 6 (11.1) 4 (8.9) 1(2.5)
<50 48 (88.9) 41 (91.1) 39(97.5)
PD‐1 categories
Toripalimab 30 (55.6)
Sintilimab 21 (38.8)
Camrelizumab 3 (5.6)

Abbreviations: AFP, alpha‐fetoprotein concentration; DCP, Des‐gamma‐carboxy prothrombin; ALT, alanine aminotransferase; AST, aspartate aminotransferase; MVI, microvascular invasion; PT, prothrombin time; TACE, transarterial chemoembolization; TB, total bilirubin; ALB, albumin; T‐L, transarterial chemoembolization plus lenvatinib; T‐L‐P, transarterial chemoembolization combined with lenvatinib plus programmed cell death protein‐1 inhibitors.