Table 2 Treatment-emergent adverse events
Patients (N = 24) | Grade 1–2 | Grade 3–4 |
|---|---|---|
Neutropenia | 8 (33) | 14 (58) |
ALT elevation | 7 (29) | 4 (17) |
AST elevation | 6 (25) | 3 (12.5) |
Infection | 8 (33) | 3 (12.5) |
Anemia | 18 (75) | 2 (8) |
Skin rash | 10 (42) | 2 (8) |
Fatigue | 18 (75) | 1 (4) |
Nausea | 6 (25) | 1 (4) |
Infusion-related reaction | 5 (21) | 1 (4) |
Peripheral neuropathy | 4 (17) | 1 (4) |
Lymphopenia | 3 (12.5) | 1 (4) |
Atrial fibrillation | 0 (0) | 1 (4) |
Thrombocytopenia | 16 (67) | 0 (0) |
Headache | 14 (58) | 0 (0) |
Diarrhea | 10 (42) | 0 (0) |
Pruritus | 7 (29) | 0 (0) |
Arthralgia | 7 (29) | 0 (0) |
Bruising | 6 (25) | 0 (0) |
Myalgia | 6 (25) | 0 (0) |
Dizziness | 5 (21) | 0 (0) |
Dry skin | 4 (17) | 0 (0) |
Sinus bradycardia | 3 (12.5) | 0 (0) |
Dysgeusia | 2 (4) | 0 (0) |