Exercise for the Prevention of Anthracycline-Induced Functional Disability and Cardiac Dysfunction: The BREXIT Study.
rct · Level II
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- Record sourced from PubMed, PMID 36342348.
- Also identified by DOI 10.1161/CIRCULATIONAHA.122.062814.
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Abstract
Breast cancer survivors treated with anthracycline-based chemotherapy (AC) have increased risk of functional limitation and cardiac dysfunction. We conducted a 12-month randomized controlled trial in 104 patients with early-stage breast cancer scheduled for AC to determine whether 12 months of exercise training (ExT) could attenuate functional disability (primary end point), improve cardiorespiratory fitness (VO<sub>2</sub>peak), and prevent cardiac dysfunction. Women 40 to 75 years of age with stage I to III breast cancer scheduled for AC were randomized to 3 to 4 days per week aerobic and resistance ExT for 12 months (n=52) or usual care (UC; n=52). Functional measures were performed at baseline, at 4 weeks after AC (4 months), and at 12 months, comprising: (1) cardiopulmonary exercise testing to quantify VO<sub>2</sub>peak and functional disability (VO<sub>2</sub>peak ≤18.0 mL·kg<sup>-1</sup>·min<sup>-1</sup>); (2) cardiac reserve (response from rest to peak exercise), quantified with exercise cardiac magnetic resonance measures to determine changes in left and right ventricular ejection fraction, cardiac output, and stroke volume; (3) standard-of-care echocardiography-derived resting left ventricular ejection fraction and global longitudinal strain; and (4) biochemistry (troponin and BNP [B-type natriuretic peptide]). Among 104 participants randomized, greater study attrition was observed among UC participants (<i>P</i>=0.031), with 93 women assessed at 4 months (ExT, n=49; UC, n=44) and 87 women assessed at 12 months (ExT, n=49; UC, n=38). ExT attenuated functional disability at 4 months (odds ratio, 0.32 [95% CI, 0.11-0.94]; <i>P</i>=0.03) but not at 12 months (odds ratio, 0.27 [95% CI, 0.06-1.12]; <i>P</i>=0.07). In a per-protocol analysis, functional disability was prevented entirely at 12 months among participants adherent to ExT (ExT, 0% versus UC, 20%; <i>P</i>=0.005). Compared with UC at 12 months, ExT was associated with a net 3.5-mL·kg<sup>-1</sup>·min<sup>-1</sup> improvement in VO<sub>2</sub>peak that coincided with greater cardiac output, stroke volume, and left and right ventricular ejection fraction reserve (<i>P</i><0.001 for all). There was no effect of ExT on resting measures of left ventricular function. Postchemotherapy troponin increased less in ExT than in UC (8-fold versus 16-fold increase; <i>P</i>=0.002). There were no changes in BNP in either group. In women with early-stage breast cancer undergoing AC, 12 months of ExT did not attenuate functional disability, but provided large, clinically meaningful benefits on VO<sub>2</sub>peak and cardiac reserve. URL: https://www.anzctr.org.au/; Unique identifier: ACTRN12617001408370.
Medical subject headings
- Heart Diseases
- Breast Neoplasms