Table 1.

AOE rates of the respective nonimatinib TKI in the major clinical trials

2-y report5-y report10-y report
PACE (ponatinib) 17.1%3  25%7  Trial ended at 5 y 
DASISION (dasatinib) None reported14  5%17  Trial ended at 5 y 
ENESTnd (nilotinib) 2% (not including peripheral arterial events)15  10.6% (300 mg)
17.9% (400 mg)18,  
24.8% (300 mg)
33.4% (400 mg)18,  
BELA (bosutinib) None reported16  N/A N/A 
BFORE (bosutinib) N/A 7.5%19  Trial ended at 5 y 
ASCEMBL (asciminib) 5.1% (2.3 y median follow-up)20  N/A N/A 
Imatinib 1 ischemic heart event in 288 patients (ENESTnd)15  2%-2.5%7,17,21 (except in BFORE: 0.4%)19  3.6% (400 mg, ENESTnd)18  
2-y report5-y report10-y report
PACE (ponatinib) 17.1%3  25%7  Trial ended at 5 y 
DASISION (dasatinib) None reported14  5%17  Trial ended at 5 y 
ENESTnd (nilotinib) 2% (not including peripheral arterial events)15  10.6% (300 mg)
17.9% (400 mg)18,  
24.8% (300 mg)
33.4% (400 mg)18,  
BELA (bosutinib) None reported16  N/A N/A 
BFORE (bosutinib) N/A 7.5%19  Trial ended at 5 y 
ASCEMBL (asciminib) 5.1% (2.3 y median follow-up)20  N/A N/A 
Imatinib 1 ischemic heart event in 288 patients (ENESTnd)15  2%-2.5%7,17,21 (except in BFORE: 0.4%)19  3.6% (400 mg, ENESTnd)18  

Imatinib cardiovascular event rates (bottom row) represent a summary of the rates in the DASISION, ENESTnd, BELA, and BFORE trials.

Kaplan-Meier estimates.

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