Table 3.
Summary of Non-Dose Limiting Toxicities Observed in 16 Evaluable Patients
Cycle 1 (16 total cycle) | Cycle 2 to 7 (15 total cycles) | |||||||
---|---|---|---|---|---|---|---|---|
Maximum grade across cycle1 | Maximum grade, cycle 2 to 6 | |||||||
Hematologic Toxicity | Grade 1 | Grade 2 | Grade 3 | Grade 4 | Grade 1 | Grade 2 | Grade 3 | Grade 4 |
Anemia | 3 | 2 | 1 | 2 | 1 | |||
Leukopenia | 5 | 1 | 1 | 1 | ||||
Lymphopenia | 4 | 1 | 1 | 2 | 1 | |||
Neutropenia | 1 | 1 | 1 | 1 | ||||
Thrombocytopenia | 6 | 2 | 2 | 1 | ||||
Non-Hematologic Toxicity* | ||||||||
Somnolence | 1 | |||||||
Fatigue | 3 | 2 | 1 | |||||
Nausea | 1 | 1 | ||||||
Vomiting | 2 | |||||||
Hypoalbuminemia | 1 | 2 | ||||||
Dizziness | 4 | 1 | ||||||
Headache | 1 | 1 | 1 |
only non-hematologic toxicities related to protocol therapy occurring in more than 10% of patients during the first cycle of VPA are listed