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. 2022 Sep 9;13:1000448. doi: 10.3389/fgene.2022.1000448

TABLE 4.

Treatment-related adverse events in patients with hepatocellular carcinoma.

Effect All grades Grade ≥3
HBV–HCC (n = 28) NBNC–HCC (n = 26) HBV–HCC (n = 28) NBNC–HCC (n = 26)
RCCEP 13 (46.4) 11 (42.3) 0 (0.0) 0 (0.0)
Proteinuria 6 (21.4) 6 (23.1) 0 (0.0) 1 (3.8)
Thrombocytopenia 5 (17.8) 4 (15.4) 0 (0.0) 1 (3.8)
Neutropenia 3 (10.7) 2 (7.7) 0 (0.0) 0 (0.0)
Leukopenia 3 (10.7) 2 (7.7) 0 (0.0) 0 (0.0)
Hypothyroidism 3 (10.7) 4 (15.4) 0 (0.0) 1 (3.8)
Hypertension 4 (14.3) 5 (19.2) 0 (0.0) 1 (3.8)
Rash 2 (7.1) 3 (11.5) 1 (3.6) 0 (0.0)
Nausea 4 (14.3) 3 (11.5) 0 (0.0) 0 (0.0)
Diarrhea 5 (17.9) 4 (15.4) 1 (3.6) 0 (0.0)
Fatigue 4 (14.3) 3 (11.5) 0 (0.0) 0 (0.0)
Myocarditis 1 (7.1) 0 (3.8) 1 (3.6) 0 (0.0)
Hyperbilirubinemia 5 (17.9) 6 (23.1) 1 (3.6) 0 (0.0)
Elevated ALT 7 (25.0) 4 (15.4) 2 (7.1) 1 (3.8)
Elevated AST 6 (21.4) 6 (23.1) 1 (3.6) 1 (3.8)

Data in brackets represent the percentages of patients. HBV–HCC, hepatitis B virus-related hepatocellular carcinoma; NBNC–HCC, non-HBV; non-HCV, hepatocellular carcinoma; RCCEP, reactive cutaneous capillary endothelial proliferation; AST, aspartate aminotransferase; ALT, alanine aminotransferase.