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. 2013 Jul-Aug;6(4 Suppl 1):S2–S9.

Table 4.

Toxicity assessment during cycles 2 to 5 of chemotherapy

Number of patients (n = 6)
Number of events (n=74)
Adverse Event Total Grade 1–2 Grade 3–4 Total Grade 1–2 Grade 3–4
Hematologic 6 6 4 38 27 11

    Anemia 4 3 2 5 3 2

    Lymphopenia 5 2 4 10 4 6

    Neutropenia 6 6 2 13 10 3

    Thrombocytopenia 5 5 0 10 10 0

Nonhematologic 6 6 2 41 38 3

    Abdominal pain 3 2 1 3 2 1

    ALP elevated 1 1 0 1 1 0

    ALT elevated 3 3 0 3 3 0

    Anorexia 1 1 0 1 1 0

    Ascites 1 1 0 1 1 0

    AST elevated 3 3 0 3 3 0

    Diarrhea 3 3 0 6 6 0

    Dizziness 2 2 0 2 2 0

    Fatigue 1 1 0 1 1 0

    Hematochezia 1 1 0 1 1 0

    Hypoalbuminemia 1 1 0 1 1 0

    Hypocalcemia 1 1 0 1 1 0

    Hypokalemia 3 3 0 3 3 0

    Mood alteration 1 1 0 1 1 0

    Nasal bleed 2 2 0 2 2 0

    Nausea 1 1 0 1 1 0

    Pruritus 1 1 0 1 1 0

    Skin fissures 1 1 0 1 1 0

    Skin rash 3 3 1 4 3 1

    Vomiting 1 1 0 1 1 0

    Weight loss 2 1 1 2 1 1

    Wheezing 1 1 0 1 1 0