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. 2019 Mar 26;12:2205–2214. doi: 10.2147/OTT.S191741

Table 3.

Adverse events of sorafenib treatment

Sorafenib (n=58) Combination Tx (n=22) p-value
All grade Grade 3/4 All grade Grade 3/4
Diarrhea 9 (15.5) 0 4 (18.2) 0 0.51
HFSR 39 (67.2) 7 (12.1) 15 (68.2) 3 (13.6) 0.58
Fatigue 7 (12.1) 0 3 (13.6) 0 0.56
Nausea/vomiting 3 (5.2) 0 2 (9.1) 0 0.42
Anorexia 8 (13.8) 0 3 (13.6) 0 0.63
Hypertension 12 (20.6) 1 (1.7) 3 (13.6) 0 0.35
Alopecia 9 (15.5) 0 4 (18.2) 0 0.51
Elevated ALT 7 (12.1) 1 (1.7) 9 (40.9) 2 (9.1) 0.01
Elevated Amy 15 (25.9) 2 (3.4) 4 (18.2) 1 (4.5) 0.34
Hyperbilirubinemia 3 (5.2) 0 2 (9.1) 0 0.42
Rash 5 (8.6) 5 (8.6) 2 (9.1) 2 (9.1) 0.63
Leukocytopenia 4 (6.9) 1 (1.7) 4 (18.2) 1 (4.5) 0.14
Thrombocytopenia 10 (17.2) 2 (3.4) 7 (31.8) 1 (4.5) 0.13

Note: Results reported as number (%).

Abbreviations: Tx, therapy; HFSR, hand–foot skin reaction; ALT, alanine aminotransferase; Amy, amylase.