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Association of Heart Failure Patients With and Without Sacubitril-Valsartan Use With Incident Cancer Risk
Wei-Syun Hu1,2, Cheng-Li Lin3
1School of Medicine, College of Medicine, China Medical University, Taichung, Taiwan.
Insights
This study investigated cancer risk in heart failure patients using sacubitril-valsartan versus those not using it. Sacubitril-valsartan use was associated with a significantly lower risk of developing cancer.
Area of Science:
- Cardiology
- Oncology
Background:
- Heart failure (HF) is a complex cardiovascular condition.
- Understanding the long-term implications of HF treatments on other health outcomes is crucial.
Purpose of the Study:
- To evaluate the association between sacubitril-valsartan use and incident cancer risk in patients with heart failure.
- To compare cancer incidence rates between patients treated with sacubitril-valsartan and a control group.
Main Methods:
- A cohort study involving 18,072 patients receiving sacubitril-valsartan and 18,072 controls.
- The Fine and Gray model was employed to estimate subhazard ratios (SHRs) for cancer development.
- Adjusted SHRs and 95% confidence intervals (CIs) were calculated.
Main Results:
- Cancer incidence rates were 12.02 per 1000 person-years (sacubitril-valsartan) vs. 23.31 per 1000 person-years (control).
- Sacubitril-valsartan users exhibited a significantly lower risk of developing cancer.
- The adjusted SHR for cancer was 0.60 (95% CI: 0.51, 0.71) for sacubitril-valsartan users.
Conclusions:
- Sacubitril-valsartan use in heart failure patients is associated with a reduced risk of incident cancer.
- Further research may explore the mechanisms behind this observed association.
Abstract:
This study was to evaluate the association between heart failure (HF) patients with and without sacubitril-valsartan use with incident cancer risk. This study consisted of 18,072 patients receiving sacubitril-valsartan and 18,072 control group participants. In the Fine and Gray model, which extends the standard Cox proportional hazards regression model, we estimated the relative risk of developing cancer between the sacubitril-valsartan cohort and the non-sacubitril-valsartan cohort by using subhazard ratios (SHRs) and 95% confidence intervals (CIs). The incidence rates of cancer were 12.02 per 1000 person-years for the sacubitril-valsartan cohort and 23.31 per 1000 person-years for the non-sacubitril-valsartan cohort. Patients receiving sacubitril-valsartan had a significantly lower risk of developing cancer with an adjusted SHR of 0.60 (0.51, 0.71). Sacubitril-valsartan users were less to be associated with the development of cancer.
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