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. Author manuscript; available in PMC: 2017 Jul 1.
Published in final edited form as: Lancet Haematol. 2016 Jun 5;3(7):e309–e316. doi: 10.1016/S2352-3026(16)30040-0

Table 2.

Adverse events at least possibly related to treatment in 24 evaluable patients treated with at least one cycle of everolimus/RCHOP-21. Includes All Grade 3+; and Grades 1 and 2 if combined incidence >10%. No grade 5 adverse events were observed.

Highest Grade/Patient
1-2 3 4
Adverse Event N % N % N %
Hematologic Anemia 9 38 3 12 0
Leukocytosis 0 2 8 0
Leukopenia 4 17 7 29 2 8
Lymphopenia 0 4 17 0
Neutropenia 4 17 0 18 75
Thrombocytopenia 15 63 3 13 3 13
Non-Hematologic Febrile neutropenia 0 5 21 0
Hypercholesterolemia 14 58 0 0
Hypertrigliceridemia 15 63 3 13 0
Hyperglycemia 0 1 4 0
Diarrhea 12 50 0 0
Nausea 3 13 0 0
Pneumonitis 3 12 1 4 0
Rash (acneiform) 0 1 4 0
Rash (maculopapular) 5 21 0 0
Dry skin 0 1 4 0
Fatigue 11 46 1 4 0
Infection 0 1 4 0
Sepsis 0 0 1 4
Urinary tract infection 0 1 4 0
Lung infection 0 1 4 0
Hypocalcemia 0 1 4 0
Hypokalemia 0 1 4 0
Hyponatremia 0 1 4 0
Hypophosphatemia 0 1 4 0
Seizure 0 1 4 0
Thromboembolic event 0 1 4 0
Alopecia 15 63 0 0
Weight loss 5 21 1 4 0
Hypoxia 0 1 4 0