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. 2021 Jun 18;9(9):957–968. doi: 10.1016/S2213-2600(21)00237-X

Table 2.

Clinical outcomes in the final analysis population

HR (95% CI) p value
Primary endpoint
Unadjusted 0·95 (0·76–1·20) 0·69
Adjusted for sex 1·01 (0·81–1·28) 0·90
Adjusted for obesity 0·99 (0·78–1·26) 0·92
Adjusted for diabetes 0·96 (0·76–1·20) 0·69
Adjusted for cardiovascular disease 0·94 (0·75–1·18) 0·59
Adjusted for all the above 1·07 (0·62–1·84) 0·82
Mortality (secondary endpoint)
Unadjusted 0·51 (0·27–0·95) 0·034
Adjusted for sex 0·47 (0·25–0·89) 0·019
Adjusted for obesity 0·46 (0·23–0·92) 0·029
Adjusted for diabetes 0·54 (0·29–1·02) 0·057
Adjusted for cardiovascular disease 0·54 (0·29–1·01) 0·055
Adjusted for all the above 0·52 (0·26–1·05) 0·068
Need for mechanical ventilation (secondary endpoint)
Unadjusted 1·07 (0·63–1·80) 0·81
Adjusted for sex 0·98 (0·58–1·67) 0·95
Adjusted for obesity 1·08 (0·63–1·86) 0·77
Adjusted for diabetes 1·13 (0·66–1·91) 0·66
Adjusted for cardiovascular disease 1·06 (0·62–1·79) 0·84
Adjusted for all the above 1·02 (0·80–1·30) 0·87

All HRs are for the imatinib group versus the placebo group. The final analysis population consisted of 188 patients in the placebo group and 197 patients in the imatinib group. HRs and 95% CIs were calculated by use of Cox regression analysis and adjusted for sex and the indicated comorbidities. HR=hazard ratio.