Skip to main content
. 2023 Sep 5;10:1435–1443. doi: 10.2147/JHC.S423684

Table 5.

Treatment-Related Adverse Events in Two Groups

Adverse Events TACE-L-P (n = 64) TACE-L (n = 58) P
Any Grade Grade 3–4 Any Grade Grade 3–4
Diarrhea 8 (12.5%) 1 (1.6%) 5 (8.6%) 1 (1.7%) 0.756
Hand-foot syndrome 11 (17.2%) 4 (6.3%) 7 (12.1%) 2 (3.4%) 0.808
Hypertension 17 (26.6%) 3 (4.7%) 13 (22.4%) 3 (5.2%) 0.764
Fatigue 23 (35.9%) 3 (4.7%) 19 (32.8%) 2 (3.4%) 0.824
Anorexia and nausea 25 (39.1%) 2 (3.2%) 21 (36.2%) 1 (1.7%) 0.678
Rash 19 (29.7%) 1 (1.6%) 20 (34.5%) 1 (1.7%) 0.972
Oral ulcer 15 (20.3%) 2 (3.1%) 13 (22.4%) 0 (0.0%) 0.492
Thyroid dysfunction 10 (15.6%) 4 (6.3%) 11 (19.0%) 2 (3.4%) 0.410
Hyperbilirubinemia 12 (18.8%) 3 (4.7%) 11 (19.0%) 3 (5.2%) 0.942
Thrombocytopenia 10 (15.6%) 2 (3.1%) 7 (12.1%) 1 (1.7%) 0.798

Note: Data were presented as n (%) or mean ± standard deviation.

Abbreviations: TACE-L-P, transarterial chemoembolization combined with lenvatinib and PD-(L)1 inhibitor; TACE-L, transarterial chemoembolization combined with lenvatinib.