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.