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. 2025 Apr 28;15(5):4387–4399. doi: 10.21037/qims-24-2067

Table 5. Treatment-related adverse events.

Adverse event Any grade Grades 3–4
HAIC (n=37) SYS (n=74) P value HAIC (n=37) SYS (n=74) P value
Rash 5 (13.5%) 25 (33.8%) 0.08 0 0
Fever 11 (29.7%) 23 (31.1%) 0.88 0 0
Abdominal pain 9 (24.3%) 10 (13.5%) 0.15 1 (2.7%) 3 (4.1%) >0.99
Vomiting 7 (18.9%) 29 (39.2%) 0.03 0 11 (14.8%) 0.04
Fatigue 4 (10.8%) 31 (41.9%) <0.01 0 0
Leukopenia 3 (8.1%) 10 (13.5%) 0.31 0 7 (9.5%) 0.12
Anemia 7 (18.9%) 36 (48.6%) <0.01 0 9 (12.2%) 0.07
Thrombocytopenia 4 (10.8%) 21 (28.4%) 0.01 0 2 (2.7%) 0.48
Elevated ALT 9 (24.3%) 33 (44.6%) 0.04 1 (2.7%) 3 (4.1%) >0.99
Elevated AST 13 (35.1%) 28 (37.8%) 0.78 1 (2.7%) 4 (5.4%) 0.60
Hyperbilirubinemia 7 (18.9%) 12 (16.2%) 0.72 2 (5.4%) 3 (4.1%) >0.99
Hypoalbuminemia 5 (13.5%) 16 (21.6%) 0.30 1 (2.7%) 0 0.48
Elevated creatinine 2 (5.4%) 9 (12.2%) 0.39 0 0
Sensory neuropathy 4 (10.8%) 18 (24.3%) 0.18 0 0

ALT, alanine transaminase; AST, aspartate transaminase; HAIC, hepatic arterial infusion chemotherapy; SYS, systemic chemotherapy.