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. 2016 Jul 1;10:2129–2136. doi: 10.2147/DDDT.S105441

Table 5.

Major toxicities during dCRT

Adverse reaction Group A (%) Group B (%) P-value
Toxicities (CTCAE 4.0)
 Overall toxicity ≥ grade 3 24 (22.9) 35 (36.5) 0.039
 Grade 3 17 (16.2) 25 (25.8) 0.094
 Grade 4 7 (6.7) 10 (10.3) 0.352
 Hematological ≥ grade 3 11 (10.5) 16 (16.5) 0.209
 Nonhematological ≥ grade 3 13 (12.4) 19 (19.6) 0.161
Hematological
 Neutropenia
  Grade 3 4 (3.8) 9 (9.2) 0.118
  Grade 4 2 (1.9) 3 (3.1) 0.587
 Thrombocytopenia
  Grade 3 5 (4.8) 4 (4.1) 1.000
  Grade 4 3 (2.9) 4 (4.1) 0.712
 Anemia
  Grade 3 1 (1.0) 5 (5.2) 0.107
  Grade 4 0 (0) 1 (1.0) 0.480
Nonhematological
 Nausea/vomiting 6 (5.7) 7 (7.2) 0.664
 Diarrhea 3 (2.9) 2 (2.1) 1.000
 Esophagitis 0 (0.0) 1 (1.0) 0.480
 Pneumonia 1 (1.0) 0 (0.0) 1.000
 Other 3 (2.9) 9 (9.3) 0.054

Abbreviations: CTCAE, Common Terminology Criteria for Adverse Events; dCRT, definitive concurrent chemoradiotherapy.