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. 2019 Jun 21;27(6):635–641. doi: 10.3727/096504018X15288447760357

Table 3.

Analysis of Adverse Events

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.