Key result
Allogeneic HCT linked to ~74% higher risk of early AF compared with autologous HCT.
Why the study?
The incidence and risk factors for early-onset atrial fibrillation following hematopoietic cell transplant remain poorly understood.
Does allogeneic hematopoietic cell transplant increase the risk of early-onset atrial fibrillation compared to autologous hematopoietic cell transplant in adults without prior cardiac disease?
Cohort (n=5,965)
No
Does allogeneic hematopoietic cell transplant increase the risk of early-onset atrial fibrillation compared to autologous hematopoietic cell transplant in adults without prior cardiac disease?
Hazard Ratio: 1.74 (95% CI 1.39–2.19)
Absolute Event Rate: 6.3% vs 4.3%
p-value: p=<0.0001
Early-onset atrial fibrillation within 90 days after hematopoietic cell transplantation is significantly more common following allogeneic compared to autologous transplant, especially in older patients and those with lower baseline functional status.
Allogeneic HCT recipients may merit closer early AF surveillance; leaves open causal mechanisms and need for prospective trials.
Atrial fibrillation (AF) is the most common acute cardiovascular complication following hematopoietic cell transplant (HCT). However, the incidence and risk factors for early-onset AF post-HCT remain poorly understood. A retrospective cohort study was conducted to assess the onset and risk factors of AF within 90 days post-HCT in 5,965 adult transplant recipients. Patients underwent either allogeneic HCT (alloHCT, n = 2,742) or autologous HCT (autoHCT, n = 3,223) between January 1st, 2010 and December 31st, 2023. Cumulative incidence curves and Gray’s tests were used to assess AF cumulative incidence. Fine-Gray proportional sub-distributional hazard models were applied to estimate associations between factors and AF risk. Among patients without prior arrhythmia, cardiac disease, or valvular heart disease, AF occurred more frequently in alloHCT recipients than in autoHCT recipients (6.3% vs. 4.3%, Gray’s test P < 0.001). The median age was 54 years (range: 18–82) for alloHCT and 59 years (range: 18–78) for autoHCT. In alloHCT recipients, increased AF risk was associated with older age (≥ 50 vs. <50 years, adjusted hazard ratio (sHR = 2.85, P < 0.0001) and lower Karnofsky performance score (KPS, < 80 vs. ≥80, adjusted sHR = 1.69, P = 0.03). In autoHCT recipients, increased AF risk was associated with older age (adjusted sHR = 2.49, P = 0.006), lower KPS (adjusted sHR = 2.41, P = 0.0001) and obesity (adjusted sHR = 1.68, P = 0.015). This study indicates that AF cumulative incidence within 90 days post-HCT is higher in alloHCT than in autoHCT patients. Transplant recipients with older age, lower KPS, or obesity have an increased risk for early onset of AF post-HCT.
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Cai et al. (2026) conducted a cohort in Hematopoietic cell transplant (HCT) (n=5,965). Allogeneic hematopoietic cell transplant (alloHCT) vs. Autologous hematopoietic cell transplant (autoHCT) was evaluated on Cumulative incidence of atrial fibrillation within 90 days post-transplant (sHR 1.74, 95% CI 1.39-2.19, p=<0.0001). Allogeneic hematopoietic cell transplantation was associated with a higher cumulative incidence of early-onset atrial fibrillation within 90 days compared to autologous transplantation (6.3% vs. 4.3%, adjusted HR 1.74).
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