Table 3.

AEs during treatment according to category

Grade ≥3 AEs 
n = 248
Grade ≥3 SAEs 
n = 102
Infection 84 41 
Febrile neutropenia 12 
Neutropenia 40 
Thrombocytopenia 
Lymphopenia 32 
Infusion-related events  11 
Tumor lysis syndrome 
Pyrexia 
Anemia 
Constitutional/musculoskeletal 
Cardiac event 
CNS (CVA, TIA, syncope, etc) 1§  
MDS 
Gastrointestinal symptoms 
Gastrointestinal perforation 
Respiratory (dyspnea, cough, etc) 
Hemorrhagic event 
Nonmelanoma skin cancer 
Skin rash 
Hypogammaglobulinemia 
Thromboembolic event 
Progressive multifocal encephalopathy 
Other 
Grade ≥3 AEs 
n = 248
Grade ≥3 SAEs 
n = 102
Infection 84 41 
Febrile neutropenia 12 
Neutropenia 40 
Thrombocytopenia 
Lymphopenia 32 
Infusion-related events  11 
Tumor lysis syndrome 
Pyrexia 
Anemia 
Constitutional/musculoskeletal 
Cardiac event 
CNS (CVA, TIA, syncope, etc) 1§  
MDS 
Gastrointestinal symptoms 
Gastrointestinal perforation 
Respiratory (dyspnea, cough, etc) 
Hemorrhagic event 
Nonmelanoma skin cancer 
Skin rash 
Hypogammaglobulinemia 
Thromboembolic event 
Progressive multifocal encephalopathy 
Other 

CNS, central nervous system; CVA, cerebrovascular accident; PML, progressive multifocal leukoencephalopathy; TIA, transient ischaemic attack.

AEs of grade 3, 4, and 5 indicate severe, life-threatening, and fatal AEs.

SAEs include fatal or life-threating events or events that caused (prolonged) hospital admission or substantial disability.

Infusion reactions were attributed to rituximab in 9 patients and to bendamustine in 2 patients (grade 3, n = 1, grade 4, n = 1, which resulted in treatment discontinuation).

§

One patient died from PML due to JC virus during follow-up.

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