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. 2013 Jan 22;31(6):724–730. doi: 10.1200/JCO.2012.42.5215

Table 2.

Treatment-Related Toxicity According to CTCAE v3.0 (N = 51)

AE Grade 1 or 2
Grade 3 or 4
No. Frequency (%) No. Frequency (%)
Nonhematologic
    Venous thromboembolism 0 0 10 20
    Infection 1 2 6 12
    Fatigue 49 96 5 10
    Increased LFTs 35 69 5 10
    Bleeding 24 47 4 8
    Constipation 39 76 3 6
    Nausea 27 53 3 6
    Pain 11 22 3 6
    Renal impairment 37 73 2 4
    Neuropathy 17 33 1 2
    Weight loss 14 27 1 2
    Hypertension 2 4 1 2
    Duodenal ulcer 1 2 1 2
    Cardiac ischemia 0 0 1 2
    Pneumonitis 0 0 1 2
    Proteinuria 0 0 1 2
    Increased amylase/lipase 1 2 1 2
    Dyspnea 17 33 0 0
    Diarrhea 16 31 0 0
    Skin toxicity 15 29 0 0
    Mucositis 12 24 0 0
    Edema 11 22 0 0
    Muscle weakness 7 14 0 0
    GI obstruction 1 2 0 0
    Fever 1 2 0 0
Hematologic
    Febrile neutropenia 0 0 1 2
    Neutropenia 32 63 16 31
    Leukopenia 44 86 12 24
    Thrombocytopenia 38 75 11 22
    Anemia 50 98 10 20
    Lymphopenia 0 0 8 16

Abbreviations: AE, adverse event; CTCAE, Common Terminology Criteria for Adverse Events; LFT, liver function test.