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Treatment-Related Adverse Events (> 20% of patients)
| Adverse Event | All Grades | Grade 3–5* |
|---|---|---|
| n (%) | n (%) | |
| Any | 31 (91) | 18 (53) |
| Nausea | 17 (50) | 2 (6) |
| Diarrhea | 12 (35) | 7 (21) |
| Anemia | 10 (29) | 4 (12) |
| Neutropenia | 10 (29) | 6 (18) |
| Fatigue | 9 (26) | 0 (0) |
| Vomiting | 7 (21) | 0 (0) |
| Tinnitus | 7 (21) | 0 (0) |
1 death occurred from sepsis possibly related to study therapy.
