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EXPLORER-HCM 研究的设计和原理:评价马卡坦特治疗有症状梗阻性肥厚型心肌病成人患者的疗效。

Study Design and Rationale of EXPLORER-HCM: Evaluation of Mavacamten in Adults With Symptomatic Obstructive Hypertrophic Cardiomyopathy.

机构信息

Brigham and Women's Hospital, Boston, MA (C.Y.H.).

Careggi University Hospital, Florence, Italy (I.O.).

出版信息

Circ Heart Fail. 2020 Jun;13(6):e006853. doi: 10.1161/CIRCHEARTFAILURE.120.006853. Epub 2020 Jun 5.

Abstract

BACKGROUND

Obstructive hypertrophic cardiomyopathy (oHCM) is characterized by unexplained left ventricular (LV) hypertrophy associated with dynamic LV outflow tract obstruction. Current medical therapies are nonspecific and have limited efficacy in relieving symptoms. Mavacamten is a first-in-class targeted inhibitor of cardiac myosin, which has been shown to reduce LV outflow tract obstruction, improve exercise capacity, and relieve symptoms of oHCM in the PIONEER-HCM phase 2 study.

METHODS

EXPLORER-HCM is a multicenter, phase 3, randomized, double-blind, placebo-controlled trial to investigate the efficacy and safety of mavacamten in treating symptomatic oHCM. Eligible adults with oHCM and New York Heart Association Functional Class II or III are randomized 1:1 to receive once-daily, oral mavacamten, or matching placebo for 30 weeks. The primary composite functional end point is clinical response at week 30 compared to baseline defined as either (1) an increase in peak oxygen consumption ≥1.5 mL/kg/min and reduction of at least one New York Heart Association class; or (2) an improvement of ≥3.0 mL/kg/min in peak oxygen consumption with no worsening of New York Heart Association class. Secondary end points include change in postexercise LV outflow tract gradient, New York Heart Association class, peak oxygen consumption, and patient-reported outcomes assessed by the Kansas City Cardiomyopathy Questionnaire and a novel HCM-specific instrument. Exploratory end points aim to characterize the effect of mavacamten on multiple aspects of oHCM pathophysiology.

CONCLUSIONS

EXPLORER-HCM is a phase 3 trial in oHCM testing a first-in-class, targeted strategy of myosin inhibition to improve symptom burden and exercise capacity through reducing LV outflow tract obstruction. Results of this trial will provide evidence to support the first disease-specific treatment for HCM. Registration: URL: https://www.clinicaltrials.gov; Unique identifier: NCT03470545.

摘要

背景

梗阻性肥厚型心肌病(oHCM)的特征是左心室(LV)肥大,原因不明,伴有动态 LV 流出道梗阻。目前的医学治疗方法是非特异性的,在缓解症状方面疗效有限。Mavacamten 是一种首创的心肌肌球蛋白靶向抑制剂,在 PIONEER-HCM 2 期研究中已证明其可减少 LV 流出道梗阻,提高运动能力,并缓解 oHCM 的症状。

方法

EXPLORER-HCM 是一项多中心、3 期、随机、双盲、安慰剂对照试验,旨在研究 mavacamten 治疗有症状的 oHCM 的疗效和安全性。符合条件的 oHCM 成人,纽约心脏协会功能分类 II 或 III 级,按 1:1 随机接受每日一次、口服 mavacamten 或匹配的安慰剂治疗 30 周。主要复合功能终点是与基线相比第 30 周的临床反应,定义为(1)峰值摄氧量增加≥1.5ml/kg/min,至少减少纽约心脏协会 1 个等级;或(2)峰值摄氧量增加≥3.0ml/kg/min,且纽约心脏协会等级无恶化。次要终点包括运动后 LV 流出道梯度、纽约心脏协会分级、峰值摄氧量和患者报告的结果的变化,通过堪萨斯城心肌病问卷和一种新的 HCM 特异性仪器进行评估。探索性终点旨在描述 mavacamten 对 oHCM 病理生理学多个方面的影响。

结论

EXPLORER-HCM 是一项 3 期试验,用于测试 oHCM 的首创、靶向肌球蛋白抑制策略,通过减少 LV 流出道梗阻来改善症状负担和运动能力。该试验的结果将为支持针对 HCM 的首个疾病特异性治疗提供证据。注册:网址:https://www.clinicaltrials.gov;唯一标识符:NCT03470545。

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