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. 2019 Sep 4;2(9):e1911838.
doi: 10.1001/jamanetworkopen.2019.11838.

Association of Early-Stage Breast Cancer and Subsequent Chemotherapy With Risk of Atrial Fibrillation

Affiliations

Association of Early-Stage Breast Cancer and Subsequent Chemotherapy With Risk of Atrial Fibrillation

Husam Abdel-Qadir et al. JAMA Netw Open. .

Abstract

Importance: Several types of cancer have been linked to a higher risk of developing atrial fibrillation (AF). Fewer data exist regarding early-stage breast cancer (EBC), for which cardio-oncology concerns are more pertinent.

Objective: To investigate the association of EBC and subsequent chemotherapy with the risk of developing AF.

Design, setting, and participants: This was a population-based, retrospective, matched cohort study conducted in Toronto, Ontario, Canada, of 68 113 women diagnosed with EBC between April 2007 and December 2016 who were matched 1:3 to a cancer-free control group based on birth year and receipt of breast imaging. Prevalence of AF before the index date (date of EBC diagnosis) was compared between the cohorts using the McNemar test. Cumulative incidence function curves were used to describe the AF incidence. To study preexisting AF, participants were matched before exclusion for prior AF. For the remaining analyses, we excluded women with prior AF before matching. An analysis was conducted beginning 1 year after the index date (ie, excluding AF diagnoses in year 1), which we stratified by chemotherapy exposure. Multivariable cause-specific regression was used to determine the hazard ratio (HR) associated with EBC relative to the controls and the association of chemotherapy with AF in patients with EBC.

Exposures: Breast cancer and chemotherapy.

Main outcomes and measures: Incidence of AF.

Results: A total of 68 113 women with EBC and 204 330 cancer-free controls were included in the study; both groups had a mean (SD) age of 60 (13) years. Of the women with EBC, 44.3% were diagnosed as having stage I breast cancer; 38.7%, stage II; and 13.4%, stage III; cancer stage information was missing for 3.6% of the patients. No difference was observed in preexisting AF prevalence (5.3% in the EBC cohort vs 5.2% in controls; P = .21). At 10 years after the index date, the AF incidence was 7.4% (95% CI, 7.1%-7.7%) for women with EBC and 6.8% (95% CI, 6.7%-7.0%) for the controls (P < .001). The adjusted cause-specific HR was significantly elevated at year 1 (HR, 2.16; 95% CI, 1.94-2.41) and after year 5 (HR, 1.20; 95% CI, 1.11-1.30) but not during years 2 through 5. Analyses beginning 1 year after diagnosis showed attenuated differences that remained statistically significant: the cumulative incidence of AF at 9-year follow-up was 7.0% (95% CI, 6.7%-7.3%) for patients with EBC and 6.5% (95% CI, 6.3%-6.7%) for the cancer-free controls. The rate of AF was higher in women who received chemotherapy (adjusted HR, 1.23; 95% CI, 1.13-1.35) but was not associated with exposure to anthracyclines or trastuzumab.

Conclusions and relevance: This study's findings suggest that patients with EBC may not have a higher prevalence of AF before cancer diagnosis. A higher rate of AF was observed in the first year and after 5 years following the EBC diagnosis. The rate of AF was higher in patients who received chemotherapy but appeared to not be associated with specific cardiotoxic agents. These findings suggest that the early and late periods of increased AF risk in EBC survivors warrant focused research to better understand the underlying causes and subsequent implications.

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Conflict of interest statement

Conflict of Interest Disclosures: Dr Abdel-Qadir reported receiving grants from the Canadian Cardiovascular Society during the conduct of the study, speaker fees from Amgen, and an honorarium for clinical events adjudication committee membership from the Canadian Vigour Centre for a study funded by AstraZeneca. Dr Amir reported receiving fees for expert testimony from Genentech (Roche) and consulting fees from Apobiologix, Sandoz, Agendia, and Myriad Genetics outside the submitted work. Dr Anderson reported receiving grants from the Canadian Institutes of Health Research (CIHR) during the conduct of the study and also outside the submitted work. No other disclosures were reported.

Figures

Figure 1.
Figure 1.. Risk of Atrial Fibrillation (AF) in Early-Stage Breast Cancer (EBC) and Cancer-Free Control Cohorts
Cumulative incidence function curves displaying the risk of AF over time among women with EBC and among cancer-free women matched on age and receipt of breast imaging before the index date.
Figure 2.
Figure 2.. Hazard Ratio of Atrial Fibrillation (AF) After Early-Stage Breast Cancer (EBC)
Adjusted cause-specific hazard ratios (HRs) for AF among patients with EBC relative to cancer-free controls. Because the proportional hazards assumption was violated, we present the HRs annually for the first 5 years. The blue horizontal dashed line at 1.00 indicates no difference. Error bars indicate 95% CI.
Figure 3.
Figure 3.. Risk of Atrial Fibrillation (AF) After the First Year Following Breast Cancer Diagnosis
Cumulative incidence function curves showing the risk of AF over time in patients with early breast cancer (EBC) and their matched controls beginning at 1 year after the index date.

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