Skip to main content
. 2021 Jan;10(1):252–261. doi: 10.21037/gs-20-593

Table 2. Summary of results for the risk ratio (RR) of adverse effects in the cyclophosphamide arm compared to control arm.

Outcomes References Participants RR (95% CI), cyclophosphamide arm compared to control arm P value Heterogeneity
P value I2 (%)
Anemia (3) 1,397 1.14 (0.35, 3.69) 0.82 0.05 68
Leucopenia (2) 1,848 3.43 (0.41, 28.43) 0.25 <0.001 100
Neutropenia (3) 1,932 1.18 (0.46, 3.02) 0.73 <0.001 99
Thrombocytopenia (3) 1,932 3.38 (1.96, 5.84) <0.001 0.48 0
Neutropenic fever (2) 1,029 0.41 (0.00, 62.18) 0.73 <0.001 96
Alopecia (3) 1,932 1.01 (0.98, 1.04) 0.66 0.48 0
Infection (2) 1,848 0.57 (0.41, 0.79) <0.001 0.90 0
Fatigue (2) 1,848 1.06 (0.57, 1.97) 0.86 0.004 88
Sensory or motor neuropathy (3) 1,396 1.57 (1.03, 2.39) 0.03 0.4 0
Mucositis (2) 1,029 0.74 (0.47, 1.17) 0.20 0.43 0
Skin changes (2) 1,848 0.69 (0.06, 8.32) 0.77 <0.001 97
Loss of appetite (2) 1,848 0.83 (0.62, 1.11) 0.21 0.34 0
Nausea or vomiting (3) 1,932 1.51 (1.11, 2.06) 0.009 0.16 46
Diarrhea (3) 1,932 0.46 (0.30, 0.68) <0.001 0.75 0
Stomatitis (2) 1,848 1.08 (0.29, 4.06) 0.91 0.002 90
Abnormal level of bilirubin (2) 1,029 0.30 (0.03, 2.82) 0.29 0.92 0
Abnormal level of AST (2) 1,029 1.86 (0.47, 7.35) 0.38 0.87 0
Abnormal level of ALT (2) 1,029 1.47 (0.34, 6.30) 0.60 0.01 84

Italic P values indicate statistical significance. RR, risk ratio; CI, confidence interval; AST, aspartate aminotransferase; ALT, alanine aminotransferase.