Tandutinib phase 1 experience: selected drug-related adverse events by CTC grade
. | . | . | . | . | . | . | . | . | Edema, grade . | . | . | . | ||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| . | . | Nausea, grade . | . | Vomiting, grade . | . | Diarrhea, grade . | . | . | Periorbital . | . | Peripheral . | . | ||||||
| Dose level, mg twice daily . | No. of patients . | 1 . | 2 . | 1 . | 2 . | 1 . | 2 . | 3 . | 1 . | 2 . | 1 . | 2 . | ||||||
| 50 | 6 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ||||||
| 100 | 3 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 0 | ||||||
| 150 | 6 | 0 | 1 | 0 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | ||||||
| 200 | 3 | 2 | 1 | 2 | 1 | 0 | 0 | 0 | 0 | 0 | 1 | 0 | ||||||
| 250 | 3 | 1 | 0 | 1 | 0 | 1 | 1 | 0 | 1 | 0 | 1 | 1 | ||||||
| 300 | 6 | 4 | 0 | 2 | 1 | 3 | 0 | 0 | 0 | 0 | 0 | 0 | ||||||
| 400 | 4 | 2 | 2 | 1 | 0 | 1 | 1 | 0 | 0 | 0 | 2 | 0 | ||||||
| 525 | 6 | 1 | 1 | 2 | 1 | 2 | 1 | 0 | 1 | 0 | 0 | 0 | ||||||
| 700 | 3 | 2 | 0 | 2 | 1 | 2 | 2 | 1 | 1 | 1 | 2 | 1 | ||||||
| Total | 40 | 14 | 5 | 10 | 5 | 11 | 5 | 1 | 3 | 1 | 8 | 2 | ||||||
. | . | . | . | . | . | . | . | . | Edema, grade . | . | . | . | ||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| . | . | Nausea, grade . | . | Vomiting, grade . | . | Diarrhea, grade . | . | . | Periorbital . | . | Peripheral . | . | ||||||
| Dose level, mg twice daily . | No. of patients . | 1 . | 2 . | 1 . | 2 . | 1 . | 2 . | 3 . | 1 . | 2 . | 1 . | 2 . | ||||||
| 50 | 6 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ||||||
| 100 | 3 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 0 | ||||||
| 150 | 6 | 0 | 1 | 0 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | ||||||
| 200 | 3 | 2 | 1 | 2 | 1 | 0 | 0 | 0 | 0 | 0 | 1 | 0 | ||||||
| 250 | 3 | 1 | 0 | 1 | 0 | 1 | 1 | 0 | 1 | 0 | 1 | 1 | ||||||
| 300 | 6 | 4 | 0 | 2 | 1 | 3 | 0 | 0 | 0 | 0 | 0 | 0 | ||||||
| 400 | 4 | 2 | 2 | 1 | 0 | 1 | 1 | 0 | 0 | 0 | 2 | 0 | ||||||
| 525 | 6 | 1 | 1 | 2 | 1 | 2 | 1 | 0 | 1 | 0 | 0 | 0 | ||||||
| 700 | 3 | 2 | 0 | 2 | 1 | 2 | 2 | 1 | 1 | 1 | 2 | 1 | ||||||
| Total | 40 | 14 | 5 | 10 | 5 | 11 | 5 | 1 | 3 | 1 | 8 | 2 | ||||||
Values in the data field indicate number of patients. Note that a patient was counted once for each grade of the adverse events experienced.