Key result
Aromatase inhibitors linked to ~175% higher risk of new-onset AF versus tamoxifen in breast cancer.
Why the study?
Aromatase inhibitors increase adverse cardiovascular events and arrhythmias in breast cancer patients, but whether they increase the risk of new-onset AF remained unclear.
Does adjunctive hormone therapy with an aromatase inhibitor increase the risk of new-onset atrial fibrillation in patients with breast cancer compared to tamoxifen?
Cohort (n=5,707)
Does adjunctive hormone therapy with an aromatase inhibitor increase the risk of new-onset atrial fibrillation in patients with breast cancer compared to tamoxifen?
Hazard Ratio: 2.75
Absolute Event Rate: 0.59% vs 0.27%
p-value: p=0.01
Aromatase inhibitor therapy in breast cancer patients is associated with a nearly 3-fold increased risk of new-onset atrial fibrillation compared to tamoxifen, warranting regular surveillance.
Aromatase inhibitors may warrant AF surveillance in breast cancer patients; extends observational signals but remains hypothesis-generating pending randomized confirmation.
Previous studies suggest that aromatase inhibitors (AIs) increase the risk of adverse cardiovascular events and cardiac arrhythmias in patients with breast cancer, but it is unclear whether AIs also increase the risk of new-onset atrial fibrillation (AF). The purpose of this study was to investigate whether the use of AIs was associated with an increased risk of new-onset AF in patients with breast cancer. We performed a retrospective analysis involving 5,707 patients with breast cancer (mean age 63.9 ± 11.2 years and 99.9% women) who received adjunctive hormone therapy with an AI (AI group, n = 4,878) or tamoxifen (tamoxifen group, n = 829) in Hong Kong between January 1, 1999, and December 31, 2020. After propensity score matching, there were 2,487 and 829 patients with balanced characteristics in the AI group and tamoxifen group, respectively. After 8,863 patient-years of follow-up, patients who were prescribed AI had a trend toward more new-onset arrhythmias compared with those prescribed tamoxifen (0.62 vs 0.30 per 100 patient-years; crude HR: 2.05; P = 0.053). The difference in arrhythmic risk was mainly driven by a higher incidence rate of new-onset AF in the AI group (0.59 vs 0.27 per 100 patient-years; crude HR: 2.18; P = 0.046). The use of AIs was confirmed to be an independent risk factor for new-onset AF on multivariate analysis (adjusted HR: 2.75; P = 0.01). Among breast cancer patients prescribed adjunctive hormonal therapy, AI was associated with an increased risk of new-onset AF. Regular surveillance for new-onset AF should be considered in breast cancer patients treated with an AI.
No takes yet. Share an insight, caveat, or question.
Ho et al. (2023) conducted a cohort in Breast cancer (n=5,707). Aromatase inhibitors vs. Tamoxifen was evaluated on New-onset atrial fibrillation (HR 2.75, p=0.01). Aromatase inhibitors increased the risk of new-onset atrial fibrillation compared to tamoxifen in breast cancer patients (0.59 vs 0.27 per 100 patient-years; adjusted HR 2.75; P=0.01).
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: