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. 2013 Aug 22;77(6):917–928. doi: 10.1111/bcp.12228

Table 7.

Comparation of AE-incidences between combination groups and single agent groups of figitumumab

AEs with a higher incidence in the combination group A* (in total 61 patients) % B (in total 76 patients) % X2 P
Decreased appetite 14 0.23 2 0.03 13.5448 0.0002
Diarrhoea 22 0.36 6 0.08 16.5150 0.0000
Thrombocytopenia 17 0.28 4 0.05 13.3236 0.0003
Neutropenia 18 0.30 0 0.00 25.8184 0.0000
Leukocytes 18 0.30 0 0.00 25.8184 0.0000
Neuropathy 16 0.26 0 0.00 22.5704 0.0000
AEs with a higher incidence in the single-agent group
Elevated AST/ALT 0 0.00 9 0.12 5.9226 0.0149
AEs with a similar incidence in the two groups
Hyperglycaemia 3 0.05 8 0.11 0.7819 0.3766
Nausea and vomiting 5 0.08 6 0.08 0.0633 0.8013
Fatigue 13 0.21 9 0.12 2.2511 0.1335
Skin reaction 0 0.00 6 0.08 3.3276 0.0681
Anaemia 13 0.21 9 0.12 2.2511 0.1335
Musculoskeletal pain 4 0.07 2 0.03 0.4843 0.4865
Pain 0 0.00 2 0.03 0.3133 0.5757
Headache 0 0.00 3 0.04 0.9637 0.3262
Weight decreased 0 0.00 2 0.03 1.6290 0.2018
Muscle spasm 0 0.00 4 0.05 3.3071 0.0690
Creatinine elevation 0 0.00 2 0.03 0.3133 0.5757
*

A, number of AEs in combination group; B, number of AEs in single agent group.