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心脏关怀试验的原理和设计:一种基于肌钙蛋白指导的神经激素阻断预防蒽环类药物心脏毒性的随机试验。

Rationale and Design of the Cardiac CARE Trial: A Randomized Trial of Troponin-Guided Neurohormonal Blockade for the Prevention of Anthracycline Cardiotoxicity.

机构信息

BHF Centre for Cardiovascular Science (P.A.H., D.E.N., N.L.M.), University of Edinburgh, United Kingdom.

Cancer Research UK, Edinburgh Centre, MRC Institute Genetics and Molecular Medicine (P.H., O.O., H.M.), University of Edinburgh, United Kingdom.

出版信息

Circ Heart Fail. 2022 Jul;15(7):e009445. doi: 10.1161/CIRCHEARTFAILURE.121.009445. Epub 2022 Jun 29.

Abstract

BACKGROUND

Anthracyclines are effective cytotoxic drugs used in the treatment of breast cancer and lymphoma but are associated with myocardial injury, left ventricular dysfunction, and heart failure. Anthracycline-induced cardiotoxicity is highly variable in severity and without a proven therapeutic intervention. β-Adrenergic receptor blockers and renin-angiotensin-system inhibitor therapies have been associated with modest cardioprotective effects in unselected patients.

METHODS

The Cardiac CARE trial is a multicentre prospective randomized open-label blinded end point trial of combination β-adrenergic receptor blocker and renin-angiotensin-system inhibitor therapy in patients with breast cancer and non-Hodgkin lymphoma receiving anthracycline chemotherapy that is associated with myocardial injury. Patients at higher risk of cardiotoxicity with plasma high-sensitivity cTnI (cardiac troponin I) concentrations in the upper tertile at the end of chemotherapy are randomized to standard of care plus combination candesartan and carvedilol therapy or standard of care alone. All patients undergo cardiac magnetic resonance imaging before and 6 months after anthracycline treatment. The primary end point is the change in left ventricular ejection fraction at 6 months after chemotherapy. In low-risk nonrandomized patients, left ventricular ejection fraction before and 6 months after anthracycline will be compared with define the specificity of the high-sensitivity cTnI assay for identifying low-risk participants who do not develop left ventricular systolic dysfunction.

DISCUSSION

Cardiac CARE will examine whether cardiac biomarker monitoring identifies patients at risk of left ventricular dysfunction following anthracycline chemotherapy and whether troponin-guided treatment with combination candesartan and carvedilol therapy prevents the development of left ventricular dysfunction in these high-risk patients.

摘要

背景

蒽环类药物是治疗乳腺癌和淋巴瘤的有效细胞毒性药物,但与心肌损伤、左心室功能障碍和心力衰竭有关。蒽环类药物诱导的心脏毒性在严重程度上差异很大,而且没有经过证实的治疗干预。β-肾上腺素能受体阻滞剂和肾素-血管紧张素系统抑制剂治疗与未选择患者的适度心脏保护作用有关。

方法

心脏护理试验是一项多中心前瞻性随机开放标签盲终点试验,研究联合β-肾上腺素能受体阻滞剂和肾素-血管紧张素系统抑制剂治疗接受蒽环类化疗的乳腺癌和非霍奇金淋巴瘤患者,这些患者的心肌损伤与蒽环类化疗有关。在化疗结束时,高敏心肌肌钙蛋白 I(cTnI)浓度在上三分之一的患者发生心脏毒性的风险较高,他们被随机分为标准治疗加联合坎地沙坦和卡维地洛治疗或单独标准治疗。所有患者在接受蒽环类药物治疗前后均进行心脏磁共振成像检查。主要终点是化疗后 6 个月左心室射血分数的变化。在低风险的非随机患者中,将比较蒽环类药物治疗前后的左心室射血分数,以确定高敏 cTnI 检测识别未发生左心室收缩功能障碍的低风险患者的特异性。

讨论

心脏护理试验将检查心脏生物标志物监测是否能识别接受蒽环类化疗后左心室功能障碍风险的患者,以及曲普尼定联合坎地沙坦和卡维地洛治疗是否能预防这些高危患者左心室功能障碍的发展。

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