Cardiovascular events reported in patients with B-cell malignancies treated with zanubrutinib.
Javid J MoslehiRichard R FurmanConstantine S TamJoe-Elie SalemChristopher R FlowersAileen CohenMeng ZhangJun ZhangLipeng ChenHan MaJennifer R BrownPublished in: Blood advances (2024)
First-generation Bruton tyrosine kinase (BTK) inhibitor, ibrutinib, has been associated with an increased risk of cardiovascular toxicities. Zanubrutinib is a more selective, next-generation BTK inhibitor. In this analysis, incidence rates of atrial fibrillation, symptomatic (grade ≥2) ventricular arrhythmia, and hypertension were evaluated in a pooled analysis of 10 clinical studies with zanubrutinib monotherapy in patients (N = 1550) with B-cell malignancies and a pooled analysis of head-to-head studies comparing zanubrutinib with ibrutinib (ASPEN cohort 1; ALPINE). Among the 10 studies, most patients (median age, 67 years) were male (66.3%) and had CLL/SLL (60.5%). Overall incidence and exposure-adjusted incidence rates (EAIR) for atrial fibrillation, symptomatic ventricular arrhythmia, and hypertension were lower with zanubrutinib than ibrutinib. Despite a similar prevalence of preexisting cardiovascular events in ASPEN and ALPINE, atrial fibrillation/flutter incidence rates (6.1% vs 15.6%) and EAIR (0.2 vs 0.64 persons per 100 person-months; P < .0001) were lower with zanubrutinib than with ibrutinib. Symptomatic ventricular arrhythmia incidence was low for both zanubrutinib (0.7%) and ibrutinib (1.7%) with numerically lower EAIR (0.02 vs 0.06 persons per 100 person-months, respectively) for zanubrutinib. The hypertension EAIR was lower with zanubrutinib than ibrutinib in ASPEN but similar between treatment arms in ALPINE. The higher hypertension EAIR in ALPINE was inconsistent with other zanubrutinib studies. However, fewer discontinuations (1 vs 14) and deaths (0 vs 6) due to cardiac disorders occurred with zanubrutinib versus ibrutinib in ALPINE. These data support zanubrutinib as a treatment option with improved cardiovascular tolerability compared with ibrutinib for patients with B-cell malignancies in need of BTK inhibitors. These trials were registered at www.ClinicalTrials.gov as # NCT03053440, NCT03336333, NCT03734016, NCT04170283, NCT03206918, NCT03206970, NCT03332173, NCT03846427, NCT02343120, and NCT03189524.
Keyphrases
- catheter ablation
- chronic lymphocytic leukemia
- tyrosine kinase
- cardiovascular events
- atrial fibrillation
- risk factors
- blood pressure
- end stage renal disease
- heart failure
- left atrial
- coronary artery disease
- left ventricular
- ejection fraction
- chronic kidney disease
- left atrial appendage
- cardiovascular disease
- epidermal growth factor receptor
- type diabetes
- oral anticoagulants
- clinical trial
- randomized controlled trial
- prognostic factors
- combination therapy
- percutaneous coronary intervention
- open label
- direct oral anticoagulants
- patient reported outcomes
- arterial hypertension
- phase iii
- optic nerve