Long-Term Risk of Heart Failure in Breast Cancer Patients After Adjuvant Chemotherapy With or Without Trastuzumab

This study sought to evaluate the long-term risk of developing heart failure (HF) in patients receiving trastuzumab therapy. Trastuzumab has improved the prognosis in patients with HER2-positive breast cancer, but it can induce left ventricular dysfunction with reduced ejection fraction or HF during...

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Published in:JACC. Heart failure Vol. 7; no. 3; pp. 217 - 224
Main Authors: Banke, Ann, Fosbøl, Emil L., Ewertz, Marianne, Videbæk, Lars, Dahl, Jordi S., Poulsen, Mikael Kjær, Cold, Søren, Jensen, Maj-Britt, Gislason, Gunnar H., Schou, Morten, Møller, Jacob E.
Format: Journal Article
Language:English
Published: United States Elsevier Inc 01-03-2019
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Summary:This study sought to evaluate the long-term risk of developing heart failure (HF) in patients receiving trastuzumab therapy. Trastuzumab has improved the prognosis in patients with HER2-positive breast cancer, but it can induce left ventricular dysfunction with reduced ejection fraction or HF during treatment. The long-term risk of HF is less well described. In a nationwide Danish retrospective cohort study, 9,901 patients scheduled for adjuvant treatment for early-stage breast cancer were identified in the Danish Breast Cancer Cooperative Group database. Of these, 8,812 patients (25% HER2-positive; 51.7 ± 8.5 years of age) received chemotherapy including anthracycline; and if they were HER2 positive, trastuzumab was added. The primary endpoint was a diagnosis of HF assessed before and after 18 months in a landmark analysis to distinguish short- and long-term risks. Median follow-up was 5.4 years (interquartile range [IQR]: 4.1 to 6.8 years). In the trastuzumab group, 60 patients had HF by 9 years versus 51 in the group who were treated with chemotherapy alone, corresponding to incidence rates per 1,000 patient years of 5.3 (95% confidence interval [CI]: 4.1 to 6.8) versus 1.4 (95% CI: 1.1 to 1.8), respectively. The cumulative incidence of HF was higher in the trastuzumab group at both the short- and long-term (p < 0.01), yielding adjusted hazard ratios of 8.7 (95% CI: 4.6 to 16.5; p < 0.01) for early HF and 1.9 (95% CI: 1.2 to 3.3; p = 0.01) for late HF associated with trastuzumab treatment. Trastuzumab treatment is associated with a 2-fold increased risk of late HF compared with chemotherapy treatment alone. [Display omitted]
ISSN:2213-1779
2213-1787
DOI:10.1016/j.jchf.2018.09.001