Key result
Women with breast cancer who received both anthracyclines and trastuzumab had a significantly higher risk of heart failure and/or cardiomyopathy compared to matched controls without breast cancer (HR 3.68).
Why the study?
Cardiovascular disease and mortality risk in women with breast cancer according to cancer therapy received relative to women without breast cancer had not been fully examined.
Do specific breast cancer therapies increase the risk of incident cardiovascular disease and mortality in women with breast cancer compared to women without breast cancer?
Population
13,642 women with invasive BC matched to 68,202 controls without BC
Comparison
Women with BC by cancer therapy received vs matched controls without BC
Design
Matched cohort study
Follow-up
Average 7 years (range < 1-14 years)
Authors
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Supports intensified cardiac monitoring after anthracycline/trastuzumab exposure; leaves open prospective validation of risk-reduction strategies.
Cohort (n=81,844)
Yes
Do specific breast cancer therapies increase the risk of incident cardiovascular disease and mortality in women with breast cancer compared to women without breast cancer?
Hazard Ratio: 3.68 (95% CI 1.79–7.59)
Absolute Event Rate: 4.4% vs 2%
p-value: p=<0.01
Women with breast cancer receiving specific therapies, particularly anthracyclines, trastuzumab, radiation, or aromatase inhibitors, have a significantly increased risk of cardiovascular events and mortality compared to women without breast cancer.
Greenlee et al. (2022) conducted a cohort in Breast cancer (n=81,844). Anthracyclines and trastuzumab vs. Matched controls without breast cancer was evaluated on Heart failure and/or cardiomyopathy (HR 3.68, 95% CI 1.79 to 7.59, p=<0.01). Women with breast cancer who received both anthracyclines and trastuzumab had a significantly higher risk of heart failure and/or cardiomyopathy compared to matched controls without breast cancer (HR 3.68).
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