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. 2020 Jun 19;4(12):2723–2735. doi: 10.1182/bloodadvances.2019001329

Table 3.

Pooled relative risk of second- and third-generation TKIs, in comparison with imatinib by toxicity

Study TKIs ENEST RCT: 300 mg TKIs ENEST RCT: 400 mg TKIs ENEST RCT: mean values of 300 and 400 mg
Outcome toxicity: grade 3-4*, No. of RCTs No. of pts RR 95% CI No. of RCTs No. of pts RR 95% CI No. of RCTs No. of pts RR 95% CI
Anemia 7 2704 1.17 0.80-1.72 7 2702 1.20 0.86-1.69 7 2703 1.19 0.83-1.70
Neutropenia 7 2704 0.69 0.46-1.02 7 2702 0.68 0.45-1.01 7 2703 0.68 0.46-1.02
Thrombocytopenia 7 2704 1.55 1.17-2.05 7 2702 1.58 1.22-2.06 7 2703 1.57 1.20-2.05
Cardiovascular events 7 2704 2.26 1.32-3.87 7 2702 2.75 1.62-4.67 7 2703 2.54 1.49-4.33
Cutaneous effects 7 2704 0.73 0.21-2.47 7 2702 1.03 0.35-2.98 7 2703 0.93 0.32-2.75
GI effects 7 2704 1.80 0.67-4.84 7 2702 2.02 0.84-4.86 7 2703 1.94 0.77-4.85
Fluid retention§ 7 2704 3.21 1.09-9.48 7 2702 2.81 0.99-7.97 7 2703 3.11 1.07-9.00
Infectious events 7 2704 1.11 0.54-2.28 7 2702 1.12 0.49-2.56 7 2703 1.11 0.54-2.28
Pancreatic effects 5 2413 2.24 1.29-3.87 5 2411 2.31 1.33-4.02 5 2412 2.29 1.32-3.96
Hepatic effects 6 2459 3.01 1.21-7.51 6 2457 3.89 1.81-8.35 6 2458 3.51 1.55-7.92
Musculoskeletal disorders 6 2658 0.76 0.36-1.62 6 2656 0.92 0.46-1.83 6 2657 0.85 0.42-1.73
QT prolongation 5 2352 0.82 0.39-1.73 5 2350 0.82 0.39-1.74 5 2351 0.82 0.39-1.73

Sensitivity analysis of different nilotinib doses (ENEST RCT: 300 mg, 400 mg, and mean values of 300 mg and 400 mg) (bosutinib BEFORE [NCT02130557], bosutinib BELA [NCT00574873], dasatinib DASISION [NCT00481247], dasatinib [NCT00070499], dasatinib NordCML006 [NCT00852566], nilotinib ENEST [NCT00471497; 300-mg and 400-mg doses], ponatinib EPIC [NCT01650805]). In ENEST RCT, the patients were randomly assigned to receive 300 mg of nilotinib (n = 282), 400 mg of nilotinib (n = 281), 400 mg of imatinib (n = 283); the number of events is presented for the 3 groups (300 mg of nilotinib, 400 mg of nilotinib, 400 mg of imatinib). The sensitivity analysis was made by introducing into the meta-analysis: first, the results of 300 mg of nilotinib; second, the results of 400 mg of nilotinib; and third, the arithmetic mean of the results of the 2 nilotinib doses.

*

National Cancer Institute Common Terminology Criteria for Adverse Events.

M-H method, random-effects method.

Bold values in these columns are statistically significant.

§

Pleural and pericardial effusion.