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. Author manuscript; available in PMC: 2017 Dec 6.
Published in final edited form as: Am J Clin Oncol. 2010 Aug;33(4):353–357. doi: 10.1097/COC.0b013e3181b0c27f

TABLE 3.

Severe (grade ≥3) Hematologic and Nonhematologic Events Occurring in 5% or More of Patients (n = 26 Patients)

Grade

3 4 5 Total




Adverse Event N % N % N % N %
Thrombocytopenia 15 57.7 5 19.2 20 76.9
Neutropenia 3 11.5 7 26.9 11* 42.3
Leukopenia 2 7.7 5 19.2 7 26.9
Anemia 6 23.1 1 3.8 7 26.9
Transfusion-pRBc 4 15.4 4 15.4
Dyspnea 3 11.5 3 11.5
Hypotension 1 3.8 2 7.7 3 11.5
Hypoxia 3 11.5 3 11.5
Vomiting 2 7.7 1 3.8 3 11.5
Diarrhea—no colostomy 3 11.5 3 11.5
Infection–ANC 3 11.5 3 11.5
Nausea 2 7.7 2 7.7
Neuromotor 2 7.7 2 7.7
Edema 2 7.7 2 7.7
Transfusion–PLT 2 7.7 2 7.7
Febrile neutropenia 2 7.7 2 7.7
*

Includes 1 patient with undefined neutropenia who were nonetheless recorded as having neutropenic fever which by definition requires an ANC <1000.

All adverse events included regardless of perceived relationship to study treatment.