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. 2017 Nov 2;2017:1068751. doi: 10.1155/2017/1068751

Table 2.

Sensitivity analysis of this study.

Outcomes N RR or WMD (95% CI) I2 Excluded the studies N RR or WMD (95% CI) I2
ORR 13 1.33 (1.12, 1.59) 0% [20, 31] 11 1.23 (1.02, 1.48) 0%
DCR 12 1.17 (1.08, 1.27) 48% [20, 31] 10 1.15 (1.05, 1.26) 51%
WBC 15 0.29 (0.20, 0.41) 0% [24, 26, 31, 32, 34] 10 0.32 (0.22, 0.48) 0%
HBG 11 0.28 (0.14, 0.54) 0% [26, 31, 32, 34] 7 0.28 (0.13, 0.59) 0%
PLT 15 0.31 (0.20, 0.47) 0% [24, 26, 31, 32, 34] 10 0.32 (0.20, 0.50) 0%
Vomiting 12 0.27 (0.17, 0.43) 0% [24, 31, 32, 34] 8 0.30 (0.17, 0.50) 0%
CD3+ 6 15.09 (11.13, 19.05) 93% [20, 27] 4 14.75 (9.33, 20.17) 88%
CD4+ 6 10.25 (7.31, 13.20) 87% [20, 27] 4 11.36 (5.76, 16.97) 83%
CD4+/CD8+ 6 0.44 (0.25, 0.63) 88% [20, 27] 4 0.38 (0.22, 0.74) 82%

Note. WBC, white blood cell; HBG, hemoglobin; PLT, platelet; N, the number of trials.