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. 2014 Aug 29;10(4):717–724. doi: 10.5114/aoms.2014.44862

Table III.

Treatment-related adverse events

Adverse events D + P (N = 118) C + P (N = 118)
Grade
3
Grade
4
Grade
3
Grade
4
n n n n
Neutropenia 41 34 33 40
Lymphopenia 1 0 4 0
Thrombocytopenia 5 0 2 1
Anemia 8 2 4 0
Dizziness 0 0 1 0
Fever 0 0 2 1
Pulmonary infection 1 0 2 0
Hyperglycemia 0 0 2 0
Fatigue 1 0 1 0
Nausea 0 0 1 0
Vomiting 2 0 1 0
Alopecia 2 2 2 1
Anorexia 0 1 1 0
Hypoproteinemia 0 0 1 0
Allergic shock 1 1 1 0
Constipation 0 0 1 0
Paclitaxel allergy 2 0 2 0
Flatulence 0 0 1 0
Cough aggravation 0 0 1 0
Extremities numbness 1 0 1 0
Diarrhea 1 0 0 1
Rash 0 0 1 0
Pruritus 0 0 0 1
ALT↑ 1 0 1 0
γ-GT↑ 0 0 1 0
Muscles or joints pains 5 0 3 0
Hypokalemia 0 2 0 0

Grade 5 events were not included in this table. Two patients experienced grade 5 events: 1 with asphyxia in the D + P arm and 1 with sudden death in the C + P arm, which were mainly attributed to progression of NSCLC. D + P – dicycloplatin plus paclitaxel, C + P – carboplatin plus paclitaxel