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. 2017 Mar;74:38–46. doi: 10.1016/j.ejca.2016.11.031

Table 2.

Grade III/IV CTCAE toxicities during treatment.

System organ class Adverse event Induction chemotherapy
CRT
Both arms (n = 85)
OxCapRT (n = 38)
CarPacRT (n = 42)
n % n % n %
Any toxicity 27 31.8 16 42.1 22 52.4
Any haematological toxicity 2 2.4 6 15.8 12 28.6
Blood and lymphatic system disorders Anaemia 1 1.2 1 2.6 0 0.0
Febrile neutropenia 0 0 0 0.0 1 2.4
Cardiac Chest pain 2 4.8 0 0.0 0 0.0
Gastrointestinal Any in this class 15 17.6 5 13.2 8 19.0
Abdominal pain 2 2.4 1 2.6 0 0.0
Colonic spasm 0 0.0 1 2.6 0 0.0
Constipation 0 0.0 1 2.6 0 0.0
Diarrhoea 7 8.2 0 0.0 1 2.4
Dry mouth 1 1.2 1 2.6 0 0.0
Dysphagia 6 7.1 2 5.3 2 4.8
GI haemorrhage 0 0.0 0 0.0 1 2.4
Mucositis 1 1.2 0 0.0 0 0.0
Nausea/vomiting 6 7.1 0 0.0 0 0.0
Oesophageal pain 0 0.0 0 0.0 1 2.4
Oesophagitis 1 1.2 2 5.3 2 4.8
General disorders Fatigue 9 10.6 4 10.5 6 14.3
Injury Fall 0 0.0 1 2.6 0 0.0
Investigations Lymphocyte decrease 0 0.0 3 7.9 3 7.1
Platelet decrease 1 1.2 1 2.6 0 0.0
Neutrophil decrease 0 0.0 1 2.6 9 21.4
White blood cell decrease 0 0.0 2 5.3 2 4.8
Metabolism Anorexia 2 2.4 2 5.3 0 0.0
Other 4 4.7 0 0.0 0 0.0
Nervous system Peripheral neuropathy 5 5.9 0 0.0 0 0.0
Pharyngolaryngeal dysaesthesia 1 1.2 0 0.0 0 0.0
Respiratory Dyspnoea 1 1.2 0 0.0 1 2.4
Vascular Hypertension 1 1.2 1 2.6 0 0.0
Hypotension 0 0.0 0 0.0 1 2.4
Peripheral ischaemia 1 1.2 0 0.0 0 0.0
Thromboembolic events 1 1.2 1 2.6 1 2.4

CTCAE, Common Terminology Criteria for Adverse Events.