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. 2021 May 18;13:4013–4029. doi: 10.2147/CMAR.S304591

Table 7.

Comparison of TACE-Related Adverse Reactions Between the TACE Plus Sorafenib and TACE Alone Treatment Groups

Adverse Event (n/%) Group χ2 P
TACE Plus Sorafenib (n=42) TACE Alone (n=43)
New ascites With 3 (7.14%) 4 (9.30%) 0.131 0.513
Without 39 (92.86%) 39 (90.70%)
Liver injury With 6 (14.29%) 7 (16.28%) 0.065 0.519
Without 36 (85.71%) 36 (83.72%)
Hepatorenal syndrome With 1 (2.38%) 1 (2.33%) 0.000 0.747
Without 41 (97.62%) 42 (97.67%)
Pleural effusion With 2 (4.76%) 3 (6.98%) 0.188 0.511
Without 40 (95.24%) 40 (93.02%)
Spontaneous bacterial peritonitis With 1 (2.38%) 0 (0.00%) 1.036 0.494
Without 41 (97.62%) 43 (100.00%)
Gastrointestinal bleeding With 2 (4.76%) 1 (2.33%) 0.370 0.491
Without 40 (95.24%) 42 (97.67%)
Ischemic cholecystitis With 2 (4.76%) 2 (4.65%) 0.001 0.683
Without 40 (95.24%) 41 (95.35%)
Liver abscess With 1 (2.38%) 1 (2.33%) 0.000 0.747
Without 41 (97.62%) 42 (97.67%)
Inguinal hematoma With 2 (4.76%) 3 (6.98%) 0.188 0.511
Without 40 (95.24%) 40 (93.02%)

Abbreviation: TACE, transarterial chemoembolization.