Skip to main content
. 2017 Nov 2;25(9):1567–1578. doi: 10.3727/096504017X14897173032733

Table 2.

Outcomes of Grades 3–5 Drug-Related Adverse Events for Capecitabine-Based Versus Capecitabine-Free Combination Adjuvant Chemotherapy in Early Breast Cancer

Grades 3–5 AEs No. of Studies Capecitabine Based n/N Capecitabine Free n/N OR [95% CI] p
Hematologic
 Neutropenia 7 1,977/4,839 2,460/4,836 0.53 (0.31–0.91) 0.02
 Febrile neutropenia 5 321/4,507 323/4,499 0.98 (0.54–1.79) 0.94
 Anemia 3 56/2,972 92/3,001 0.61 (0.43–0.85) 0.03
 Thrombocytopenia 4 44/2,706 11/2,725 3.39 (0.67–17.17) 0.14
Gastrointestinal
 Nausea 5 111/2,632 117/2,671 0.96 (0.73–1.25) 0.76
 Vomiting 6 120/3,343 159/3,338 0.74 (0.58–0.94) 0.01
 Diarrhea 6 224/3,343 89/3,338 2.77 (1.64–4.67) 0.0001
Others
 HFS 7 672/4,839 80/4,836 13.47 (6.96–26.07) <0.001
 Fatigue 5 311/3,204 309/3,199 1.05 (0.79–1.39) 0.76
 Mucositis 5 208/3,204 115/3,199 2.24 (1.17–4.30) 0.02
 Myalgia 5 72/3,204 181/3,199 0.42 (0.23–0.76) 0.004

AEs, adverse events; HFS, hand–foot syndrome.