Abstract
Purpose
Cardiotoxicities are adverse effects often reported in chemotherapy-treated breast cancer patients. This study evaluated the potential risk factors and cumulative incidence of doxorubicin-induced cardiotoxicity in Korean breast cancer patients.
Methods
We retrospectively analyzed the data of 613 breast cancer patients who underwent a multigated acquisition (MUGA) scan or echocardiography prior to chemotherapy and at least one post-chemotherapy follow-up MUGA scan/echocardiography between 2007 and 2016 at National Cancer Center, Korea. The Cox proportional hazards models were used to evaluate cardiotoxicity risks. Competing risks analyses were performed to estimate cumulative incidence of cardiotoxicity.
Results
Risk factors associated with cardiotoxicity within 2 years of doxorubicin administration included age [adjusted hazard ratio (aHR) = 1.02, 95% confidence interval (CI) 1.00–1.04; p = 0.05], metastasis (aHR = 2.66; 95% CI 1.36–5.20; p < 0.01), and concomitant trastuzumab (aHR = 4.08; 95% CI 2.31–7.21; p < 0.01). The cumulative incidence of patients with cardiotoxicity was 6.1% at 2 years (without substantial change from about 9 months)and 20.2% at 2 years (without substantial change from about 15 months) after initiation of doxorubicin-containing therapy without and with trastuzumab, respectively.
Conclusions
Susceptibility to chemotherapy-induced cardiotoxicity within 2 years of doxorubicin initiation in breast cancer patients was elevated with old age, metastasis, and concomitant trastuzumab. Regular imaging monitoring at least up to 9 months after doxorubicin initiation in patients treated without concomitant trastuzumab, and 15 months in patients treated with concomitant trastuzumab, is needed for early detection of chemotherapy-induced cardiotoxicity.
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Funding
This work was supported by grants from the National Cancer Center (NCC1710321-1, 1810301-1, 1710300-3, 1831140-1), Republic of Korea.
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HC: Conceptualization, methodology, and writing—original draft. SL: data curation, formal analysis, and writing—review and editing. SHS: validation and writing—review and editing. IHP: validation and writing—review and editing. KSL: validation and writing—review and editing. MHK: validation and writing—review and editing. HJK: conceptualization, supervision, and writing—original draft.
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All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards. The study protocol and data were approved by the Institutional Review Board of the National Cancer Center (NCC2017-0013) in Korea.
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Cho, H., Lee, S., Sim, S.H. et al. Cumulative incidence of chemotherapy-induced cardiotoxicity during a 2-year follow-up period in breast cancer patients. Breast Cancer Res Treat 182, 333–343 (2020). https://doi.org/10.1007/s10549-020-05703-5
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DOI: https://doi.org/10.1007/s10549-020-05703-5