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. 2010 Oct 12;103(9):1349–1355. doi: 10.1038/sj.bjc.6605943

Table 3. Grade 3–4 adverse events.

  FOLFOX4 (N=52) 5FU-cisplatin (N=43)
  n (%) n (%)
Number of patients with any grade 3 or 4 adverse events 39 (75.0) 31 (72.1)
Haematological 39 (75.0) 31 (72.1)
 Neutropenia 12 (23.1) 9 (20.9)
 Thrombocytopenia 5 (9.6) 5 (11.6)
 Febrile neutropenia 5 (9.6) 2 (4.7)
 Anaemia 2 (3.8) 3 (7.0)
 Leucopenia 3 (5.8) 1 (2.3)
 Febrile bone marrow aplasia 1 (1.9) 1 (2.3)
 Pancytopenia 1 (1.9) 1 (2.3)
Dysphagia 10 (19.2) 7 (16.3)
Radiation-related oesophagitis 4 (5.8) 6 (14.0)
Stomatitis 3 (5.8) 0
Odynophagia 1 (1.9) 2 (4.7)
Oesophageal pain 1 (1.9) 1 (2.3)
Asthenia 4 (7.7) 4 (9.3)
Mucosal inflammation 4 (7.7) 1 (2.3)
Fatigue 2 (3.8) 2 (4.7)
Chest pain 0 2 (4.7)
Neutropenic infection 2 (3.8) 2 (4.7)
Weight decreased 2 (3.8) 2 (4.7)
Anorexia 2 (3.8) 2 (4.7)
Hypocalcaemia 0 2 (4.7)