Real-world impact of atrial fibrillation (AFib) on cardiovascular (CV) outcomes and healthcare resource utilization (HCRU) in patients with chronic lymphocytic leukemia (CLL)

ASCO 2026CLLZanubrutinibPoster

Michael Fradley, MD

DISCLAIMER

The contents of the presentations above are designed for educational and scientific exchange purposes and are not promotional. They may contain information on investigational products or investigational uses of approved products. No conclusions regarding safety and/or efficacy for such investigational products or uses may be made.

 
SUMMARY

This retrospective observational study assessed the association between atrial fibrillation (AF) and cardiovascular outcomes and healthcare resource utilization among adults newly diagnosed with chronic lymphocytic leukemia (CLL). Using data from the Symphony database, patients diagnosed between 2014 and 2024 were followed for one year after CLL diagnosis. Among 233,362 patients, 13.1% were reported to have AF within one year. Patients with AF had a higher likelihood of at least one inpatient visit than those without AF (54.9% vs 23.2%; P<0.0001) and were more likely to incur inpatient services (odds ratio, 2.28; 95% CI, 2.21–2.35). Higher proportions of patients with AF experienced subsequent stroke, bleeding, and heart failure compared with those without AF (all P<0.0001). Among patients initiating firstline Bruton tyrosine kinase inhibitors, AF within one year occurred in 11% with zanubrutinib, 13% with acalabrutinib, and 16% with ibrutinib (P<0.0001). In patients with AF, lower rates of cardiovascular outcomes (P<0.002) and inpatient service use (P<0.0001) were reported with firstline zanubrutinib compared with acalabrutinib and ibrutinib.

Population Intervention Comparator Outcome Measures
Adults newly diagnosed with chronic lymphocytic leukemia identified in the Symphony database between 2014 and 2024 Zanubrutinib, ibrutinib, and acalabrutinib N/A Incidence of atrial fibrillation, subsequent cardiovascular outcomes and healthcare resource utilization

FAQs

The objective of the study was to evaluate the impact of atrial fibrillation (AF) on cardiovascular outcomes and healthcare resource utilization in adults newly diagnosed with chronic lymphocytic leukemia (CLL).

This retrospective observational study used data from the Symphony database to identify adults newly diagnosed with CLL between 2014 and 2024. Patients were followed for one year after diagnosis to assess the incidence of AF. Subsequent cardiovascular outcomes, including stroke, bleeding, and heart failure, as well as healthcare resource utilization (inpatient, outpatient, and other services), were compared between patients with and without AF. Multivariable regression analyses were conducted to assess associations between AF and these outcomes. Exploratory analyses evaluated outcomes by firstline Bruton tyrosine kinase inhibitor therapy, including ibrutinib, acalabrutinib, and zanubrutinib.

Among 233,362 newly diagnosed patients with CLL, 13.1% had AF within 1 year of diagnosis. Patients with AF had a higher likelihood of at least one inpatient visit compared with those without AF (54.9% vs 23.2%; P<0.0001) and were more likely to incur inpatient services (odds ratio [OR], 2.28; 95% CI, 2.21–2.35). Higher proportions of patients with AF experienced subsequent stroke (14.3% vs 8.9%), bleeding (27.9% vs 19.1%), and heart failure (54.5% vs 18.9%) than those without AF (all P<0.0001). Age ≥65 years, male sex, nonWhite race, and AF were associated with these outcomes (P<0.01).

 
Among patients initiating firstline BTKis, AF within one year occurred in 11% with zanubrutinib, 13% with acalabrutinib, and 16% with ibrutinib (P<0.0001). Compared to first-line ibrutinib and first-line acalabrutinib, a lower proportion of patients with AF treated with firstline zanubrutinib had subsequent stroke (12.2% vs 9.4% vs 4.8%, respectively; P<0.002), bleeding (27.4% vs 21.5% vs 17.4%; P<0.002), heart failure (50.9% vs 45.6% vs 39.6%; P<0.002), and inpatient service use (46.4% vs 51.5% vs 60.4%; P<0.0001).

You are now leaving the website

This link is provided for information purposes only. You’ll be leaving beonemedaffairs.com and accessing a third-party website over which [BeOne Medicines | GmbH] has no control or influence.

This link will take you to a third-party website outside of beonemedaffairs.com.

[BeOne Medicines | GmbH] has no control over this website and makes no representations regarding its content or availability in your location. [BeOne Medicines | GmbH] declines any responsibility for third-party information, data usage policies, or personal data processing.

By proceeding, you acknowledge that you are part of the intended audience of the third-party website and confirm your compliance with applicable laws.

Do you want to leave beonemedaffairs.com

You are now leaving the the website beonemedaffairs.com and entering another BeOne website with different terms of use. Information included on this website may not be specific to your country. Click Continue to proceed