Table 3.

Multivariate predictors of MACEs during ibrutinib use

VariableHR95% CIP
New/worsened HTN vs no/stable HTN* 2.17 (1.08-4.38) .03 
Age ≥ 60 1.78 (1.06-2.99) .03 
BMI ≥30 1.30 (0.84-2.02) .24 
Male 1.80 (1.05-3.09) .03 
Prior AF 0.72 (0.24-2.21) .57 
Prior CAD 1.38 (0.77-2.48) .27 
Prior CHF 2.71 (1.36-5.39) .01 
Prior CVE 0.91 (0.34-2.39) .85 
Prior DM 1.29 (0.74-2.25) .37 
Prior CKD 1.22 (0.75-1.99) .43 
VariableHR95% CIP
New/worsened HTN vs no/stable HTN* 2.17 (1.08-4.38) .03 
Age ≥ 60 1.78 (1.06-2.99) .03 
BMI ≥30 1.30 (0.84-2.02) .24 
Male 1.80 (1.05-3.09) .03 
Prior AF 0.72 (0.24-2.21) .57 
Prior CAD 1.38 (0.77-2.48) .27 
Prior CHF 2.71 (1.36-5.39) .01 
Prior CVE 0.91 (0.34-2.39) .85 
Prior DM 1.29 (0.74-2.25) .37 
Prior CKD 1.22 (0.75-1.99) .43 

n = 562. MACE includes the combined outcome of AF, CHF, CVE, myocardial infarction, ventricular fibrillation/ventricular tachycardia, and cardiovascular death during ibrutinib use. Bold P values indicate statistically significant results.

AF, atrial fibrillation; CAD, coronary artery disease; CHF, congestive heart failure; CVE, cerebrovascular event; TIA, transient ischemic attack.

*

Nontime-varying HTN.

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