Abstract
Ibrutinib increases the risk of atrial fibrillation (AF), but the associated risk factors are not clearly defined. We performed retrospective review of ibrutinib-treated patients in a large academic practice to identify risk factors for new-onset AF. Variables with p-values <.05 in logrank analysis were included as pairs in two-variable Cox regression. Of the 168 patients treated with ibrutinib, 60.7% had chronic lymphocytic leukemia/small lymphocytic lymphoma and 39.3% other histologies. The incidence of AF was 11.9% after a median 154-day ibrutinib exposure. Only heart failure (hazard ratio, 95% confidence interval; 14.1, 5.3–37.2) and left atrial abnormality on electrocardiogram (5.4, 1.9–15.4) were independently significant in paired Cox regression. Eighty-seven percent of patients with HF satisfied Framingham clinical criteria. As structural heart disease is a strong risk factor for incident AF, we emphasize the importance of baseline electrocardiogram, recommend baseline clinical screening for HF and, in specific instances, a baseline echocardiogram.
Original language | English (US) |
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Pages (from-to) | 1447-1453 |
Number of pages | 7 |
Journal | Leukemia and Lymphoma |
Volume | 60 |
Issue number | 6 |
DOIs | |
State | Published - May 12 2019 |
Funding
This work was supported by the Northwestern Medicine Enterprise Data Warehouse under NIH grant UL1TR001422. SM received research funding and honorarium for consulting and speaking activities from Pharmacyclics and Janssen.
Keywords
- Atrial fibrillation
- Bruton’s tyrosine kinase inhibitor
- cardio-oncology
- heart failure
- ibrutinib
- left atrial abnormality
ASJC Scopus subject areas
- Hematology
- Oncology
- Cancer Research