Myosin Inhibition in Patients With Obstructive Hypertrophic Cardiomyopathy Referred for Septal Reduction Therapy

被引:231
作者
Desai, Milind Y. [1 ,2 ,3 ]
Owens, Anjali [4 ]
Geske, Jeffrey B. [5 ]
Wolski, Kathy [2 ,3 ]
Naidu, Srihari S. [6 ]
Smedira, Nicholas G. [1 ,2 ]
Cremer, Paul C. [3 ]
Schaff, Hartzell [7 ]
McErlean, Ellen [2 ,3 ]
Sewell, Christina [2 ,3 ]
Li, Wanying [8 ]
Sterling, Lulu [8 ]
Lampl, Kathy [8 ]
Edelberg, Jay M. [8 ]
Sehnert, Amy J. [8 ]
Nissen, Steven E. [2 ,3 ]
机构
[1] Cleveland Clin, Hypertroph Cardiomyopathy Ctr, Cleveland, OH 44195 USA
[2] Cleveland Clin, Dept Cardiovasc Med, Heart Vasc & Thorac Inst, Cleveland, OH 44195 USA
[3] Cleveland Clin, Heart Vasc & Thorac Inst, Cleveland Clin Coordinating Ctr Clin Res, Cleveland, OH 44195 USA
[4] Univ Penn, Div Cardiol, Philadelphia, PA 19104 USA
[5] Mayo Clin, Dept Cardiovasc Dis, Rochester, MN USA
[6] Westchester Med Ctr, Dept Cardiol, Valhalla, NY USA
[7] Mayo Clin, Dept Cardiovasc Surg, Rochester, MN USA
[8] MyoKardia Inc, Brisbane, CA USA
关键词
mavacamten; obstructive HCM; randomized clinical trial; septal reduction; LEFT-VENTRICULAR OUTFLOW; LONG-TERM SURVIVAL; TRACT OBSTRUCTION; HEALTH-STATUS; EXPLORER-HCM; DOUBLE-BLIND; TASK-FORCE; MYECTOMY; MAVACAMTEN; OUTCOMES;
D O I
10.1016/j.jacc.2022.04.048
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND Septal reduction therapy (SRT), surgical myectomy or alcohol ablation, is recommended for obstructive hypertrophic cardiomyopathy (oHCM) patients with intractable symptoms despite maximal medical therapy, but is associated with morbidity and mortality. OBJECTIVES This study sought to determine whether the oral myosin inhibitor mavacamten enables patients to improve sufficiently to no longer meet guideline criteria or choose to not undergo SRT. METHODS Patients with left ventricular (LV) outflow tract (LVOT) gradient >= 50 mm Hg at rest/provocation who met guideline criteria for SRT were randomized, double blind, to mavacamten, 5 mg daily, or placebo, titrated up to 15 mg based on LVOT gradient and LV ejection fraction. The primary endpoint was the composite of the proportion of patients proceeding with SRT or who remained guideline-eligible after 16 weeks' treatment. RESULTS One hundred and twelve oHCM patients were enrolled, mean age 60 +/- 12 years, 51% men, 93% New York Heart Association (NYHA) functional class III/IV, with a mean post-exercise LVOT gradient of 84 +/- 35.8 mm Hg. After 16 weeks, 43 of 56 placebo patients (76.8%) and 10 of 56 mavacamten patients (17.9%) met guideline criteria or underwent SRT, difference (58.9%; 95% CI: 44.0%-73.9%; P < 0.001). Hierarchical testing of secondary outcomes showed significant differences (P < 0.001) favoring mavacamten, mean differences in post-exercise peak LVOT gradient -37.2 mm Hg; >= 1 NYHA functional class improvement 41.1%; improvement in patient-reported outcome 9.4 points; and NT-proBNP and cardiac troponin I between-groups geometric mean ratio 0.33 and 0.53. CONCLUSIONS In oHCM patients with intractable symptoms, mavacamten significantly reduced the fraction of patients meeting guideline criteria for SRT after 16 weeks. Long-term freedom from SRT remains to be determined. (C) 2022 The Authors. Published by Elsevier on behalf of the American College of Cardiology Foundation.
引用
收藏
页码:95 / 108
页数:14
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