Table 2.
Maximum severitya (Grade 3+) AEs, Per patient (N=35)
| Adverse event | Grade 3 | Grade 4 |
|---|---|---|
| Thrombocytopenia | 4 (11%) | 0 |
| Anemia | 2 (6%) | 0 |
| Diarrhea | 2 (6%) | 0 |
| Fatigue | 2 (6%) | 0 |
| Rash/Desquamation | 1 (3%) | 0 |
| Thrombosis | 0 | 2 (6%) |
| Hepatic failure | 0 | 1 (3%) |
| SGOT (AST) | 3 (9%) | 0 |
| SGPT (ALT) | 2 (6%) | 0 |
| Hyponatremia | 2 (6%) | 0 |
| Ileus | 1 (3%) | 0 |
| Hyperglycemia | 1 (3%) | 0 |
| Hypoglycemia | 0 | 1 (3%) |
| Hypotension | 1 (3%) | 0 |
| Muscle weakness | 1 (3%) | 0 |
| Dizziness | 1 (3%) | 0 |
| Cognitive disorder | 1 (3%) | 0 |
NCI CTCAE V3.0. Reported are AEs deemed at least possibly related to BORTEZOMIB