Mavacamten: Real-World Experience from 22 Months of the Risk Evaluation and Mitigation Strategy (REMS) Program.

IF 7.8 1区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS
Milind Y Desai, Dewey Seto, Michael Cheung, Sonia Afsari, Niki Patel, Arnaud Bastien, Jeffrey Lockman, Michele Coiro, Matthew W Martinez
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引用次数: 0

Abstract

Background: Mavacamten is the only cardiac myosin inhibitor approved by the US FDA for treatment of symptomatic New York Heart Association class II-III obstructive hypertrophic cardiomyopathy (HCM) patients. Under the risk evaluation and mitigation strategy (REMS) program for mavacamten, patients are required to be monitored for development of systolic heart failure, and reduction of left ventricular ejection fraction (LVEF) to <50%. We report results from the mavacamten REMS database (28-Apr-2022 to 27-Feb-2024). Methods: Data on healthcare providers and pharmacy certification, patient monitoring (from Patient Status Forms, based partly on echocardiograms), and screening for drug interactions prior to each dispense were collected. Results: Of 6,299 patients who received ≥1 dose of mavacamten, 60.0% were women; 64.6% were >60 years of age. Of 5,573 patients with submitted Patient Status Forms, 256 (4.6%) developed LVEF <50% and 71 (1.3%) experienced heart failure requiring hospitalization (HFH). On the 29,111 status forms in these patients, each representing an assessment of an echocardiogram, LVEF <50% was reported on 276 (0.9%) and HFH was reported on 86 (0.3%). Of 1,929 patients with ≥1 year of treatment, 78 (4.0%) had an LVEF reduction to <50% and 4 (0.2%) experienced LVEF <50% + HFH but later resumed treatment. Of 3,228 patients initiated on 5 mg/day mavacamten and were treated for at least 6 months, 2,391 (74.1%) remained at 5 or 10 mg/day. At 3- and 6-months following mavacamten treatment initiation, 57.2% and 70.3%, respectively, demonstrated post-Valsalva LV outflow tract gradient <30 mmHg. Conclusions: We describe the feasibility and experience of the first 22 months of the REMS program for prescribing mavacamten in >6,000 symptomatic obstructive HCM patients. The need for temporary interruption for LVEF <50% was low, including for patients on therapy ≥1 year, with even fewer LVEF reductions associated with HFH.

Mavacamten:风险评估和缓解策略 (REMS) 计划实施 22 个月的实际经验。
背景:Mavacamten 是美国 FDA 批准用于治疗有症状的纽约心脏协会 II-III 级阻塞性肥厚型心肌病 (HCM) 患者的唯一一种心肌酶抑制剂。根据 mavacamten 的风险评估和缓解策略 (REMS) 计划,患者必须接受监测,以防出现收缩性心力衰竭和左心室射血分数 (LVEF) 下降至方法值:收集有关医疗服务提供者和药房认证、患者监测(来自患者状态表,部分基于超声心动图)以及每次配药前药物相互作用筛查的数据。结果在 6299 名接受过≥1 次玛伐康定治疗的患者中,60.0% 为女性;64.6% 年龄大于 60 岁。在提交了患者状态表的 5573 名患者中,256 人(4.6%)出现了 LVEF:我们介绍了 REMS 计划实施前 22 个月的可行性和经验,在超过 6,000 名有症状的阻塞性 HCM 患者中处方了马伐康坦。需要暂时中断 LVEF
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来源期刊
Circulation: Heart Failure
Circulation: Heart Failure 医学-心血管系统
CiteScore
12.90
自引率
3.10%
发文量
271
审稿时长
6-12 weeks
期刊介绍: Circulation: Heart Failure focuses on content related to heart failure, mechanical circulatory support, and heart transplant science and medicine. It considers studies conducted in humans or analyses of human data, as well as preclinical studies with direct clinical correlation or relevance. While primarily a clinical journal, it may publish novel basic and preclinical studies that significantly advance the field of heart failure.
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