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. 2013 Dec 13;7(2):461–467. doi: 10.3892/etm.2013.1449

Table III.

Specific treatment-related adverse events.

Adverse event, grade FOLFOX, n=87 (%) EOX, n=26 (%) t/χ2 P-value
Neutropenia
 0 20 (23) 6 (23.1) 1.708 0.635
 I 25 (28.7) 7 (26.9)
 II 38 (43.7) 10 (38.5)
 III 4 (4.6) 3 (11.5)
Anemia 0.099 0.952
 0 41 (47.1) 13 (50)
 I 27 (31) 8 (30.8)
 II 19 (21.8) 5 (19.2)
Thrombocytopenia 0.326 0.850
 0 77 (88.5) 23 (88.5)
 I 9 (10.3) 3 (11.5)
 II 1 (1.1) 0 (0)
Nausea and vomiting 10.812 0.029
 0 1 (1.1) 0 (0)
 I 15 (17.2) 5 (19.2)
 II 53 (60.9) 13 (50)
 III 18 (20.7) 5 (19.2)
 IV 0 (0) 3 (11.5)
Peripheral neuropathy 1.601 0.449
 0 53 (60.9) 15 (57.7)
 I 25 (28.7) 10 (38.5)
 II 9 (10.3) 1 (3.8)
Hand-foot syndrome 4.237 0.040
 0 73 (83.9) 17 (65.4)
 I 14 (16.1) 9 (34.6)
ALT/AST increase 0.001 0.980
 0 60 (69) 18 (69.2)
 I 27 (31) 8 (30.8)

ALT, alanine transferase; AST, aspartate transferase.