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. 2019 Oct 1;8(16):6955–6966. doi: 10.1002/cam4.2555

Table 3.

Adverse events observed in >2 patients who received at least one cycle of RBMD

Grades 1‐2 Grades 3‐4
RBMD (%) R‐maintenance (%) RBMD (%) R‐maintenance (%)
Hematological
Lymphopenia 12 (20) 25 (56.82) 42 (70) 11 (25)
Neutropenia 11 (18.3) 14 (31.8) 36 (60) 12 (27.3)
Anemia 38 (63.3) 17 (38.6) 1 (1.7) 1 (2.3)
Thrombocytopenia 34 (56.7) 14 (31.8) 2 (3.3) 1 (2.3)
Nonhematological
Fatigue 13 (21.7) 2 (4.5) 1 (1.7)
Infections 11 (18.3) 13 (27.5) 5 (8.3)a 4 (9.1)
Fever (nonneutropenic) 9 (15) 2 (4.5) 2 (3.3)
Vomiting 8 (13.3)
Infusion reactions 6 (10) 2 (3.3)
Constipation 5 (8.3)
Pain 5 (8.3) 4 (9.1)
Diarrhea 4 (6.7) 1 (1.7)
Nausea 3 (5)
Rash 3 (5) 1 (2.3)
Febrile neutropenia 4 (6.7) 2 (4.5)

Adverse events recorded during induction and maintenance therapy in 60 patients who received at least one cycle of RBMD and were included in the toxicity analysis.

Abbreviations: RBMD, rituximab, bendamustine, mitoxantrone, and dexamethasone; R‐maintenance, rituximab maintenance therapy.

a

One patient had grade 5 infection and died from septic shock due to influenza A infection.