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. 2022 Oct 20;12:945915. doi: 10.3389/fonc.2022.945915

Table 3.

Treatment-related adverse events.

AEs TACE+L n=91n, (%) TACE+L+PD-1 n=75n, (%)
Any Grade ≥ Grade 3 Any Grade ≥ Grade 3
Hypertension 11 (12.1) 3 (3.3) 19 (25.3) 6 (8.0)
Fatigue 10 (10.1) 2 (2.2) 10 (13.3) 4 (5.3)
Diarrhea 7 (7.7) 0 (0) 7 (9.3) 4 (5.3)
Decreased appetite 8 (8.8) 2 (2.2) 8 (10.7) 3 (4.0)
Nausea 7 (7.7) 0 (0) 7 (9.3) 3 (4.0)
Palmar-plantar Erythrodysesthesia syndrome 1 (1.1) 0 (0) 4 (5.3) 1 (1.3)
Proteinuria 0 (0) 0 (0) 1 (1.3) 0 (0)
Abnormal liver function 0 (0) 0 (0) 2 (2.6) 1 (1.3)
Thrombocytopenia 0 (0) 0 (0) 1 (1.3) 0 (0)
Abdominal pain 0 (0) 0 (0) 1 (1.3) 1 (1.3)
Hypothyroidism 0 (0) 0 (0) 1 (1.3) 0 (0)
Rash 1 (1.1) 0 (0) 1 (1.3) 0 (0)

TACE, transarterial chemoembolization; PD-1, anti-PD-1 blockade.