Table 2.
3-AP dose cohorts: no. of patients (%)
|
||||
---|---|---|---|---|
50 mg/m2, N=7 | 75 mg/m2, N=15 | 100 mg/m2, N=3 | All patients, N=25 | |
Toxicity | ||||
Nausea/vomiting | ||||
Grade 1/2 | 7 | 8 | 3 | 18 (72) |
Grade 3/4 | 0 | 0 | 0 | 0 |
Fever | ||||
Grade1/2 | 5 | 8 | 0 | 13 (52) |
Grade3/4 | 0 | 0 | 0 | 0 |
Diarrhea | ||||
Grade1/2 | 4 | 6 | 2 | 12(48) |
Grade3/4 | 0 | 0 | 0 | 0 |
Rash | ||||
Grade1/2 | 2 | 4 | 1 | 7 (28) |
Grade 3/4 | 2 | 0 | 0 | 2 (8) |
Mucositis | ||||
Grade1/2 | 3 | 5 | 1 | 9 (36) |
Grade 3/4 | 0 | 0 | 0 | 0 |
LFTs | ||||
Grade 1/2 | 0 | 0 | 0 | 0 |
Grade 3/4 | 1 | 1 | 1 | 3 (12) |
Cerebellar | ||||
Grade 1/2 | 0 | 0 | 0 | 0 |
Grade 3/4 | 0 | 2a | 0 | 2 (8) |
Denotes dose-limiting cerebellar toxicity occurring in two patients