Table 3.

Adverse events reported on study, regardless of attribution

Overall population (N = 10)Any grade, n (%)Grade 3/4, n (%)Grade 5, n (%)
Nonhematologic    
 Fatigue 4 (40)   
 Infusion reaction 2 (20)   
 Abdominal pain 2 (20)   
 Anorexia 2 (20)   
 Vomiting 2 (20)   
 Diarrhea 2 (20)   
 Constipation 2 (20)   
 Cough 2 (20)   
 Dyspnea 2 (20)   
 Depression 2 (20)   
 Rash 1 (10) 1 (10)  
 Peripheral neuropathy 1 (10)*   
Hematologic    
 Neutropenia  3 (30)  
 Anemia 2 (20) 1 (10)  
 Thrombocytopenia  1 (10)  
Serious adverse events    
 Intracranial hemorrhage   1 (10) 
 Portal vein thrombosis  1 (10)  
 Epiglottitis  1 (10)  
 Pleural effusion  1 (10)  
Overall population (N = 10)Any grade, n (%)Grade 3/4, n (%)Grade 5, n (%)
Nonhematologic    
 Fatigue 4 (40)   
 Infusion reaction 2 (20)   
 Abdominal pain 2 (20)   
 Anorexia 2 (20)   
 Vomiting 2 (20)   
 Diarrhea 2 (20)   
 Constipation 2 (20)   
 Cough 2 (20)   
 Dyspnea 2 (20)   
 Depression 2 (20)   
 Rash 1 (10) 1 (10)  
 Peripheral neuropathy 1 (10)*   
Hematologic    
 Neutropenia  3 (30)  
 Anemia 2 (20) 1 (10)  
 Thrombocytopenia  1 (10)  
Serious adverse events    
 Intracranial hemorrhage   1 (10) 
 Portal vein thrombosis  1 (10)  
 Epiglottitis  1 (10)  
 Pleural effusion  1 (10)  
*

Pretreatment grade 1 neuropathy worsened to grade 2 after 1 cycle of BV, but subsequently returned to baseline without dose modification.

All grade 4 events, required dose holds for 1 wk (n = 1) and 3 wk (n = 2); 1 patient required dose reduction of BV for cycle 7 after 2 successive dose holds.

All SAEs were considered unrelated to BV.

Patient died of an intracranial hemorrhage resulting from a mechanical fall during cycle 1 of BV in the setting of thrombocytopenia.

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