Effect of Mavacamten on Echocardiographic Features in Symptomatic Patients With Obstructive Hypertrophic Cardiomyopathy
Jazyk angličtina Země Spojené státy americké Médium print
Typ dokumentu klinické zkoušky, fáze III, časopisecké články, multicentrická studie, randomizované kontrolované studie, práce podpořená grantem
PubMed
34915982
DOI
10.1016/j.jacc.2021.09.1381
PII: S0735-1097(21)07900-6
Knihovny.cz E-zdroje
- Klíčová slova
- N-terminal pro–B-type natriuretic peptide, diastolic function, hypertrophic cardiomyopathy, mavacamten,
- MeSH
- benzylaminy farmakologie terapeutické užití MeSH
- biologické markery krev MeSH
- dvojitá slepá metoda MeSH
- echokardiografie MeSH
- hypertrofická kardiomyopatie krev diagnostické zobrazování farmakoterapie MeSH
- lidé středního věku MeSH
- lidé MeSH
- senioři MeSH
- srdce účinky léků MeSH
- srdeční myosiny antagonisté a inhibitory MeSH
- tolerance zátěže účinky léků MeSH
- uracil analogy a deriváty farmakologie terapeutické užití MeSH
- Check Tag
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- klinické zkoušky, fáze III MeSH
- multicentrická studie MeSH
- práce podpořená grantem MeSH
- randomizované kontrolované studie MeSH
- Názvy látek
- benzylaminy MeSH
- biologické markery MeSH
- MYK-461 MeSH Prohlížeč
- srdeční myosiny 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
Citace poskytuje Crossref.org
ClinicalTrials.gov
NCT03470545