Skip to main content
. 2024 Nov 15;16(11):4392–4401. doi: 10.4251/wjgo.v16.i11.4392

Table 5.

Treatment-related adverse events in the two groups, n (%)

Adverse events
D-TACE-P-L (n = 50)
C-TACE-P-L (n = 54)
P value
Any grade
Grade 3
Any grade
Grade 3
Diarrhea 9 (18.0) 2 (4.0) 7 (13.0) 1 (1.8) 0.717
Hand-foot syndrome 12 (24.0) 2 (4.0) 15 (27.8) 2 (3.7) 0.882
Hypertension 13 (26.0) 1 (2.0) 14 (26.0) 0 (0.0) 0.572
Fatigue 24 (48.0) 4 (8.0) 20 (37.0) 3 (5.6) 0.522
Anorexia and nausea 26 (52.0) 4 (8.0) 30 (55.6) 5 (9.3) 0.928
Rash 19 (38.0) 1 (2.0) 25 (46.3) 3 (5.6) 0.518
Thyroid dysfunction 6 (12.0) 0 (0.0) 10 (18.5) 1 (1.8) 0.485
Hyperbilirubinemia 11 (22.0) 2 (4.0) 9 (16.7) 1 (1.8) 0.738
Fever 46 (92.0) 6 (12.0) 48 (89.9) 3 (5.6) 0.462
Abdominal pain 34 (68.0) 6 (12.0) 33 (61.1) 2 (3.7) 0.336

C-TACE-P-L: Conventional transarterial chemoembolization combined with lenvatinib plus programmed cell death 1 inhibitor; D-TACE-P-L: Drug-eluting beads transarterial chemoembolization combined with lenvatinib plus programmed cell death 1 inhibitor.