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.