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. 2022 May 10;20:154. doi: 10.1186/s12916-022-02361-w

Table 2.

Treatment-related adverse events occurring in ≥10% of patients

Adverse event All grades a Apatinib (n = 25), n (%)
Grade 1 Grade 2 Grade 3
Fatigue 22 (88) 13 (52) 7 (28) 2 (8)
Hand-foot syndrome 20 (80) 5 (20) 10 (40) 5 (20)
AST increased 17 (68) 16 (64) 1 (4)
Proteinuria 16 (64) 7 (28) 6 (24) 3 (12)
Thrombocytopenia 16 (64) 13 (52) 3 (12)
Diarrhea 16 (64) 9 (36) 7 (28)
Headache 15 (60) 13 (52) 2 (8)
Nausea 14 (56) 10 (40) 3 (12) 1 (4)
Decreased appetite 14 (56) 11 (44) 3 (12)
Dizziness 14 (56) 13 (52) 1 (4)
Hypertension 13 (52) 5 (20) 8 (32)
Urine occult blood 12 (48) 11 (44) 1 (4)
Anemia 12 (48) 7 (28) 5 (20)
ALT increased 11 (44) 9 (36) 2 (8)
Mucositis oral 10 (40) 5 (20) 4 (16) 1 (4)
WBC decreased 10 (40) 6 (24) 4 (16)
Blood bilirubin increased 10 (40) 7 (28) 3 (12)
Hyponatremia 10 (40) 10 (40)
Vomiting 10 (40) 7 (28) 2 (8) 1 (4)
Neutrophilic granuloaytopenia 9 (36) 5 (20) 3 (12) 1 (4)
Cough 8 (32) 8 (32)
Creatinine increased 7 (28) 5 (20) 2 (8)
Hypochloremia 5 (20) 5 (20)
Lymphocytopenia 5 (20) 1 (4) 1 (4) 3 (12)
Weight loss 5 (20) 5 (20)
Chest distress 5 (20) 4 (16) 1 (4)
Hoarseness 4 (16) 4 (16)
Hypertriglyceridemia 4 (16) 4 (16)
GGT increased 3 (12) 2 (8) 1 (4)
Constipation 3 (12) 3 (12)

aNo grade 4 or 5 adverse events occurred

ALT alanine transaminase, AST aspartate transferase, GGT gamma-glutamyltransferase, WBC white blood cell count