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. 2018 Jan 8;50(4):1304–1315. doi: 10.4143/crt.2017.463

Table 4.

Cumulative adverse events during treatment by maximum grade per patient during treatment

Adverse event Toxic effect
p-valuea)
IC+CCRT (n=43)
CCRT (n=62)
All grades Grade 3-4
All grades 1 2 3 4 All grades 1 2 3 4
Leucopenia 39 (90.7) 8 19 12 0 40 (93.0) 18 16 6 0 1 0.112
Neutropenia 36 (83.7) 7 15 12 2 22 (51.2) 11 8 3 0 0.001 0.003
Anemia 32 (74.4) 21 8 2 1 17 (39.5) 12 4 1 0 0.001 0.609
Thrombocytopenia 12 (27.9) 8 4 0 0 9 (20.9) 6 3 0 0 0.451 -
AST increased 8 (18.6) 8 0 0 0 2 (4.7) 2 0 0 0 0.044 -
ALT increased 21 (48.8) 18 3 0 0 8 (18.6) 8 0 0 0 0.003 -
BUN 5 (11.6) 5 0 0 0 1 (2.3) 1 0 0 0 0.204 -
CRE 4 (9.3) 4 0 0 0 1 (2.3) 1 0 0 0 0.357 -
Mucositis 38 (88.4) 14 17 7 0 42 (97.7) 13 23 6 0 0.204 0.763
Dermatitis 33 (76.7) 25 7 1 0 34 (79.1) 24 9 1 0 0.795 > 0.999
Vomiting 28 (65.1) 17 9 2 0 32 (74.4) 21 9 2 0 0.348 > 0.999

Values are presented as number (%). IC, induction chemotherapy; CCRT, concurrent chemoradiotherapy; AST, aspartate amino transferase; ALT, alanine amino transferase; BUN, blood urea nitrogen; CRE, creatinine.

a)

p-values were calculated using a chi-square test (or Fisher exact test).