Effect of Mavacamten on Echocardiographic Features in Symptomatic Patients With Obstructive Hypertrophic Cardiomyopathy
Language English Country United States Media print
Document type Clinical Trial, Phase III, Journal Article, Multicenter Study, Randomized Controlled Trial, Research Support, Non-U.S. Gov't
PubMed
34915982
DOI
10.1016/j.jacc.2021.09.1381
PII: S0735-1097(21)07900-6
Knihovny.cz E-resources
- Keywords
- N-terminal pro–B-type natriuretic peptide, diastolic function, hypertrophic cardiomyopathy, mavacamten,
- MeSH
- Benzylamines pharmacology therapeutic use MeSH
- Biomarkers blood MeSH
- Double-Blind Method MeSH
- Echocardiography MeSH
- Cardiomyopathy, Hypertrophic blood diagnostic imaging drug therapy MeSH
- Middle Aged MeSH
- Humans MeSH
- Aged MeSH
- Heart drug effects MeSH
- Cardiac Myosins antagonists & inhibitors MeSH
- Exercise Tolerance drug effects MeSH
- Uracil analogs & derivatives pharmacology therapeutic use MeSH
- Check Tag
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Clinical Trial, Phase III MeSH
- Multicenter Study MeSH
- Research Support, Non-U.S. Gov't MeSH
- Randomized Controlled Trial MeSH
- Names of Substances
- Benzylamines MeSH
- Biomarkers MeSH
- MYK-461 MeSH Browser
- Cardiac Myosins MeSH
- Uracil MeSH
BACKGROUND: EXPLORER-HCM (Clinical Study to Evaluate Mavacamten [MYK-461] in Adults With Symptomatic Obstructive Hypertrophic Cardiomyopathy) demonstrated that mavacamten, a cardiac myosin inhibitor, improves symptoms, exercise capacity, and left ventricular outflow tract (LVOT) obstruction in patients with obstructive hypertrophic cardiomyopathy (oHCM). OBJECTIVES: The purpose of this study was to evaluate mavacamten's effect on measures of cardiac structure and function and its association with changes in other clinical measures. METHODS: Key echocardiographic parameters from serial echocardiograms over 30 weeks from 251 symptomatic oHCM patients (mavacamten [n = 123], placebo [n = 128]) were assessed in a core laboratory. RESULTS: More patients on mavacamten (80.9%; n = 76 of 94) vs placebo (34.0%; n = 33 of 97) showed complete resolution of mitral valve systolic anterior motion after 30 weeks (difference, 46.8%; P < 0.0001). Mavacamten also improved measures of diastolic function vs placebo, including left atrial volume index (LAVI) (mean ± SD baseline: 40 ± 12 mL/m2 vs 41 ± 14 mL/m2; mean change from baseline of -7.5 mL/m2 [95% CI: -9.0 to -6.1 mL/m2] vs -0.09 mL/m2 [95% CI: -1.6 to 1.5 mL/m2]; P < 0.0001) and lateral E/e' (baseline, 15 ± 6 vs 15 ± 8; change of -3.8 [95% CI: -4.7 to -2.8] vs 0.04 [95% CI: -0.9 to 1.0]; P < 0.0001). Among mavacamten-treated patients, improvement in resting, Valsalva, and post-exercise LVOT gradients, LAVI, and lateral E/e' was associated with reduction in N-terminal pro-B-type natriuretic peptide (P ≤ 0.03 for all). Reduction in LAVI was associated with improved peak exercise oxygen consumption (P = 0.04). CONCLUSIONS: Mavacamten significantly improved measures of left ventricular diastolic function and systolic anterior motion. Improvement in LVOT obstruction, LAVI, and E/e' was associated with reduction in a biomarker of myocardial wall stress (N-terminal pro-B-type natriuretic peptide). These findings demonstrate improvement in important markers of the pathophysiology of oHCM with mavacamten. (Clinical Study to Evaluate Mavacamten [MYK-461] in Adults With Symptomatic Obstructive Hypertrophic Cardiomyopathy; NCT03470545).
Department of Cardiology Thoraxcenter Erasmus Medical Center Rotterdam Rotterdam the Netherlands
Department of Cardiovascular Diseases Mayo Clinic Phoenix Arizona USA
Division of Cardiovascular Medicine Brigham and Women's Hospital Boston Massachusetts USA
Duke University School of Medicine Durham North Carolina USA
Heart Institute Hadassah University Medical Center Jerusalem Israel
Institute of Cardiovascular Science University College London London United Kingdom
Methodist DeBakey Heart and Vascular Center Houston Texas USA
MyoKardia Inc a wholly owned subsidiary of Bristol Myers Squibb Brisbane California USA
UCSF HCM Center of Excellence University of California San Francisco San Francisco California USA
References provided by Crossref.org
ClinicalTrials.gov
NCT03470545