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. 2023 Nov 22;13:1235786. doi: 10.3389/fonc.2023.1235786

Table 4.

Treatment-related adverse events.

AEs Any grade Grade 3/4
TO
(N = 64)
TA
(N = 32)
p TO
(N = 64)
TA
(N = 32)
p
Abdominal pain 25 (39.1) 12 (37.5) 0.882 3 (4.7) 1 (3.1) <0.001
Nausea 22 (34.4) 10 (31.3) 0.759 0 (0) 0 (0) 1.000
Diarrhea 12 (18.8) 7 (21.9) 0.717 0 (0) 1 (3.1) 0.333
Decreased appetite 20 (31.3) 15 (46.9) 0.165 1 (1.6) 2 (6.3) 0.534
Erythra 0 (0) 5 (15.6) 0.006 0 (0) 2 (6.3) 0.109
Fatigue 6 (9.4) 5 (15.6) 0.571 0 (0) 0 (0) 1.000
Hypoproteinemia 12 (18.8) 5 (15.6) 0.656 2 (3.1) 0 (0) 0.551
Elevated bilirubin 10 (15.6) 6 (18.8) 0.699 1 (1.6) 1 (3.1) 1.000
Elevated transaminases 30 (46.9) 18 (56.3) 0.386 3 (4.7) 2 (6.3) 0.749
Hypothyroidism 0 (0) 6 (18.8) 0.001 0 (0) 1 (3.1) 0.333
Decreased PLT 9 (14.1) 8 (25.0) 0.186 0 (0) 0 (0) 1.000
Hypertension 3 (4.7) 6 (18.8) 0.063 0 (0) 0 (0) 1.000
Hand–foot skin reaction 0 (0) 8 (25.0) <0.001 0 (0) 2 (6.3) 0.109
Dysphonia 0 (2) 2 (6.3) 0.109 0 (0) 0 (0) 1.000
Proteinuria 2 (3.1) 5 (15.6) 0.071 0 (0) 0 (0) 1.000
Bleeding (gingiva) 1 (1.6) 4 (12.5) 0.081 0 (0) 1 (3.1) 0.333
Joint pain 0 (4) 4 (12.5) 0.012 0 (0) 0 (0) 1.000

TO, TACE only; TA, TACE combined with anlotinib; TACE, transarterial chemoembolization; AEs, adverse events; PLT, platelet count.