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. 2021 Aug 4;11:632168. doi: 10.3389/fonc.2021.632168

Table 2.

Meta-analysis results of adverse drug reactions (ADRs).

Outcomes Trials Experimental group (Events/Total) Control group (Events/Total) SM RR, 95%CI I2 P
Neutropenia 20 269/698 416/696 REM 0.65 [0.54, 0.79] 79% <0.00001
Anemia 13 135/379 195/375 REM 0.68 [0.52, 0.89] 70% 0.005
Thrombocytopenia 20 155/602 237/595 REM 0.65 [0.51, 0.82] 62% 0.0004
Nausea and vomiting 19 263/647 377/646 REM 0.73 [0.64, 0.82] 32% <0.00001
Diarrhea 10 62/307 111/301 REM 0.58 [0.45, 0.75] 0% <0.0001
Hepatic dysfunction 14 45/442 86/446 REM 0.55 [0.40, 0.77] 0% 0.0005
Renal dysfunction 10 14/324 34/323 REM 0.48 [0.26, 0.88] 0% 0.02
Neurotoxicity 12 123/389 162/379 REM 0.78 [0.65, 0.92] 0% 0.004
Alopecia 4 50/145 61/138 REM 0.77 [0.61, 0.97] 0% 0.03
Stomatitis 6 45/174 62/174 REM 0.73 [0.53, 1.00] 0% 0.05

RR, risk ratio; CI, confidence interval; SM, statistical method; REM, random-effect model.