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. 2017 Nov 2;10:171. doi: 10.1186/s13045-017-0537-5

Table 5.

Documented treatment-emergent all-grade adverse events in ≥ 10% of patients (safety population)

L (n = 13) L + R (n = 11) L + other (n = 34) Overall (N = 58)
No. % No. % No. % No. %
Hematologic
 Anemia 2 15 3 27 5 15 10 17
 Thrombocytopenia 1 8 1 9 7 21 9 16
 Neutropenia 1 8 1 9 6 18 8 14
 Pancytopenia 1 8 3 27 3 9 7 12
 Febrile neutropenia 0 0 0 0 6 18 6 10
Nonhematologic
 Fatigue 4 31 4 36 14 41 22 38
 Nausea 2 15 2 18 7 21 11 19
 Dizziness 2 15 2 18 7 21 11 19
 Dyspnea 2 15 3 27 6 18 11 19
 Peripheral edema 0 0 2 18 9 26 11 19
 Rash 2 15 1 9 7 21 10 17
 Cough 1 8 3 27 7 21 11 19
 Decreased appetite 2 15 0 0 5 15 7 12
 Diarrhea 0 0 1 9 7 21 8 14
 Headache 3 23 1 9 2 6 6 10
 Pyrexia 1 8 0 0 5 15 6 10
 Vomiting 0 0 2 18 4 12 6 10
 Constipation 0 0 0 0 6 18 6 10
Laboratory investigations
 Platelet count decreased 2 15 1 9 3 9 6 10
 White blood cell count decreased 1 8 1 9 4 12 6 10

L lenalidomide, L + R lenalidomide plus rituximab