Adverse events in induction
Event . | All patients (N = 34) . |
---|---|
Grade 3/4 infections | 23 patients 30 episodes MDI, n = 10 (gram negative, n = 7*; gram positive, n = 2†; candidemia, n = 1) Febrile neutropenia without MDI or CDI, n = 8 Probable fungal pneumonia, n = 11 Bacterial pneumonia, n = 1‡ |
Pneumothorax | 1 |
Pancreatitis | 1 |
Grade 3/4 neuropathy | 0 |
Cardiac arrhythmia | 1 |
Septic cardiomyopathy | 1 |
CNS bleed | 1 |
GI bleed | 1 |
Intestinal obstruction | 1 |
Portal vein thrombosis | 1 (died during maintenance due to upper GI bleed) |
Infusion reactions (rituximab-related) grade 3/4 | 0 |
Tumor lysis syndrome | 3 |
Death during induction (due to gram-negative sepsis) | 1 |
Event . | All patients (N = 34) . |
---|---|
Grade 3/4 infections | 23 patients 30 episodes MDI, n = 10 (gram negative, n = 7*; gram positive, n = 2†; candidemia, n = 1) Febrile neutropenia without MDI or CDI, n = 8 Probable fungal pneumonia, n = 11 Bacterial pneumonia, n = 1‡ |
Pneumothorax | 1 |
Pancreatitis | 1 |
Grade 3/4 neuropathy | 0 |
Cardiac arrhythmia | 1 |
Septic cardiomyopathy | 1 |
CNS bleed | 1 |
GI bleed | 1 |
Intestinal obstruction | 1 |
Portal vein thrombosis | 1 (died during maintenance due to upper GI bleed) |
Infusion reactions (rituximab-related) grade 3/4 | 0 |
Tumor lysis syndrome | 3 |
Death during induction (due to gram-negative sepsis) | 1 |