Table 3.
Adverse Event | Apatinib Plus Chemotherapy [n (%)] | |
---|---|---|
Any Grade | Grade 3 or 4 | |
Hematological | ||
Leukopenia | 8 (40%) | 1 (5%) |
Neutropenia | 6 (30%) | 1 (5%) |
Anemia | 4 (20%) | 0 (0) |
Thrombocytopenia | 3 (15%) | 0 (0) |
Nonhematologic | ||
Proteinuria | 4 (20%) | 1 (5%) |
Hypertension | 9 (45%) | 1 (10%) |
Hand-foot syndrome | 5 (25%) | 2 (10%) |
Elevated transaminase | 3 (15%) | 1 (5%) |
Hyperbilirubinemia | 2 (10%) | 0 (0) |
Bleeding | 2 (10%) | 0 (0) |
Fatigue | 11 (55%) | 0 (0) |
ALP increased | 1 (5%) | 0 (0) |
Elevated GGT | 1 (5%) | 0 (0) |
Abdominal pain | 4 (20%) | 0 (0) |
Decreased appetite | 6 (30%) | 0 (0) |
Hypoproteinemia | 1 (5%) | 0 (0) |
Diarrhea | 4 (20%) | 0 (0) |
Elevated LDH | 1 (5%) | 0 (0) |
Oral ulcer | 1 (5%) | 0 (0) |
Stomatitis | 1 (5%) | 1 (5%) |
Dysphagia | 1 (5%) | 0 (0) |
Dysphonia | 2 (10%) | 0 (0) |
Rash | 2 (10%) | 0 (0) |
Adverse events are listed if they were reported in at least 5% of patients in either treatment group. ALP, alkaline phosphatase; GGT, g-glutamyl transferase; LDH, lactate dehydrogenase.