Henriksen, Peter A. and Hall, Peter and MacPherson, Iain R. and Joshi, Shruti S. and Singh, Trisha and Maclean, Morag and Lewis, Steff and Rodriguez, Aryelly and Fletcher, Alexander and Everett, Russell J. and Stavert, Harriet and Broom, Angus and Eddie, Lois and Primrose, Lorraine and McVicars, Heather and McKay, Pam and Borley, Annabel and Rowntree, Clare and Lord, Simon and Collins, Graham and Radford, John and Guppy, Amy and Williams, Michelle C. and Japp, Alan and Payne, John R. and Newby, David E. and Mills, Nick L. and Oikonomidou, Olga and Lang, Ninian N. (2023) Multicenter, prospective, randomized controlled trial of high-sensitivity cardiac troponin I–guided combination angiotensin receptor blockade and beta-blocker therapy to prevent anthracycline cardiotoxicity: The Cardiac CARE trial. Circulation, 148 (21). pp. 1680-1690. ISSN 0009-7322
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BACKGROUND:
Anthracycline-induced cardiotoxicity has a variable incidence, and the development of left ventricular dysfunction is preceded by elevations in cardiac troponin concentrations. Beta-adrenergic receptor blocker and renin-angiotensin system inhibitor therapies have been associated with modest cardioprotective effects in unselected patients receiving anthracycline chemotherapy.
METHODS:
In a multicenter, prospective, randomized, open-label, blinded end-point trial, patients with breast cancer and non-Hodgkin lymphoma receiving anthracycline chemotherapy underwent serial high-sensitivity cardiac troponin testing and cardiac magnetic resonance imaging before and 6 months after anthracycline treatment. Patients at high risk of cardiotoxicity (cardiac troponin I concentrations in the upper tertile during chemotherapy) were randomized to standard care plus cardioprotection (combination carvedilol and candesartan therapy) or standard care alone. The primary outcome was adjusted change in left ventricular ejection fraction at 6 months. In low-risk nonrandomized patients with cardiac troponin I concentrations in the lower 2 tertiles, we hypothesized the absence of a 6-month change in left ventricular ejection fraction and tested for equivalence of ±2%.
RESULTS:
Between October 2017 and June 2021, 175 patients (mean age, 53 years; 87% female; 71% with breast cancer) were recruited. Patients randomized to cardioprotection (n=29) or standard care (n=28) had left ventricular ejection fractions of 69.4±7.4% and 69.1±6.1% at baseline and 65.7±6.6% and 64.9±5.9% 6 months after completion of chemotherapy, respectively. After adjustment for age, pretreatment left ventricular ejection fraction, and planned anthracycline dose, the estimated mean difference in 6-month left ventricular ejection fraction between the cardioprotection and standard care groups was −0.37% (95% CI, −3.59% to 2.85%; P=0.82). In low-risk nonrandomized patients, baseline and 6-month left ventricular ejection fractions were 69.3±5.7% and 66.4±6.3%, respectively: estimated mean difference, 2.87% (95% CI, 1.63%–4.10%; P=0.92, not equivalent).
CONCLUSIONS:
Combination candesartan and carvedilol therapy had no demonstrable cardioprotective effect in patients receiving anthracycline-based chemotherapy with high-risk on-treatment cardiac troponin I concentrations. Low-risk nonrandomized patients had similar declines in left ventricular ejection fraction, bringing into question the utility of routine cardiac troponin monitoring. Furthermore, the modest declines in left ventricular ejection fraction suggest that the value and clinical impact of early cardioprotection therapy need to be better defined in patients receiving high-dose anthracycline.
Title | Multicenter, prospective, randomized controlled trial of high-sensitivity cardiac troponin I–guided combination angiotensin receptor blockade and beta-blocker therapy to prevent anthracycline cardiotoxicity: The Cardiac CARE trial |
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Creators | Henriksen, Peter A. and Hall, Peter and MacPherson, Iain R. and Joshi, Shruti S. and Singh, Trisha and Maclean, Morag and Lewis, Steff and Rodriguez, Aryelly and Fletcher, Alexander and Everett, Russell J. and Stavert, Harriet and Broom, Angus and Eddie, Lois and Primrose, Lorraine and McVicars, Heather and McKay, Pam and Borley, Annabel and Rowntree, Clare and Lord, Simon and Collins, Graham and Radford, John and Guppy, Amy and Williams, Michelle C. and Japp, Alan and Payne, John R. and Newby, David E. and Mills, Nick L. and Oikonomidou, Olga and Lang, Ninian N. |
Identification Number | 10.1161/CIRCULATIONAHA.123.064274 |
Date | 21 November 2023 |
Divisions | College of Medical Veterinary and Life Sciences > School of Cancer Sciences College of Medical Veterinary and Life Sciences > School of Cardiovascular & Metabolic Health College of Medical Veterinary and Life Sciences > School of Medicine, Dentistry & Nursing |
Publisher | American Heart Association |
Additional Information | Dr Henriksen acknowledges the financial support of National Health Service Research Scotland, through National Health Service Lothian. Dr Henriksen is chief investigator for the Cardiac CARE Study (EudraCT 2017-000896-99, ISRCTN24439460), which is funded by the Efficacy and Mechanism Evalua-tion Programme (funding reference 15/48/20), a Medical Research Council and NIHR partnership, and the British Heart Foundation. Dr Mills is supported by the British Heart Foundation through a chair award (CH/F/21/90010), program grant (RG/20/10/34966), and research excellent award (RE/18/5/34216). The funders had no role in the study or the decision to submit this work to be considered for publication. Dr Lang is supported by a British Heart Foundation Centre of Research excellence award (RE/18/6/34217). The views expressed in this publication are those of the authors and not necessarily those of the MRC, National Health Service, NIHR, or Department of Health. The Efficacy and Mech-anism Evaluation Programme is funded by MRC and NIHR, with contributions from CSO in Scotland and NISCHR in Wales, and the HSC R&D Division, public health agency, in Northern Ireland. |
URI | https://pub.demo35.eprints-hosting.org/id/eprint/457 |
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Item Type | Article |
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Depositing User | Unnamed user with email ejo1f20@soton.ac.uk |
Date Deposited | 11 Jun 2025 16:38 |
Revision | 16 |
Last Modified | 11 Jun 2025 16:38 |
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