Treatment Response to Mavacamten in Patients With Obstructive Hypertrophic Cardiomyopathy: 96-Week Results From the EXPLORER Cohort of the MAVA–Long-Term Extension Cardiac Magnetic Resonance Imaging Substudy

All participants provided written informed consent?a In EXPLORER-HCM. patients received mavacamten or placebo for 30 weeks. After trial completion and a variable washout period, patients could enroll in MAVA- LTE. with initiation of mavacamten 5 mg/day and echocardiography-guided titration. CMR assessments were conducted as previously detailed? with analyses at baseline and week 30 of EXPLORER-HCM and weeks |24 and 96 of MAVA-LTE (data extraction on March 9, (2023). Exploratory end points included left ventricular (LV) mass index, LV maximum wall thickness, volumes land function (left atrial volume maximum index, LV end- diastolic volume index, LV end-sys tolic volume index, and myocardial contractile fraction), focal and diffuse mocar- dial fibrosis (6-SD late gadolinium enhancement [LGE] and average extracellular volume fraction), and LV ejec- tion fraction (LVEF).

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Publication Details

Journal
Circulation
Published
2025-09-22
DOI
https://doi.org/10.1161/circulationaha.124.071188
Citations
1
Primary Topic
Cardiomyopathy and Myosin Studies
Type
article
Field-Weighted Citation Impact
1.39
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article

Treatment Response to Mavacamten in Patients With Obstructive Hypertrophic Cardiomyopathy: 96-Week Results From the EXPLORER Cohort of the MAVA–Long-Term Extension Cardiac Magnetic Resonance Imaging Substudy

Theodore P. Abraham, Roberto Barriales‐Villa, Artur Oręziak, John C. Stendahl et al.
1 citations
Circulation
Cardiomyopathy and Myosin Studies
1.39
article

Treatment Response to Mavacamten in Patients With Obstructive Hypertrophic Cardiomyopathy: 96-Week Results From the EXPLORER Cohort of the MAVA–Long-Term Extension Cardiac Magnetic Resonance Imaging Substudy

Theodore P. Abraham, Roberto Barriales‐Villa, Artur Oręziak, John C. Stendahl, Ganesh Balaratnam, Ofer Havakuk, Sara Saberi, Iacopo Olivotto, Shawna Fox, Nuno Cardim, Christopher M. Kramer, ANJALI TIKU OWENS, Tim Seidler, Mark V. Sherrid, Neal K. Lakdawala, Michael Jerosch‐Herold, Ahmad Masri, Florian Rader, Sheila M. Hegde, Raymond Y. Kwong, Lubna Choudhury, Andrew Wang, Gregory Kurio
article en
1 citations

Abstract

All participants provided written informed consent?a In EXPLORER-HCM. patients received mavacamten or placebo for 30 weeks. After trial completion and a variable washout period, patients could enroll in MAVA- LTE. with initiation of mavacamten 5 mg/day and echocardiography-guided titration. CMR assessments were conducted as previously detailed? with analyses at baseline and week 30 of EXPLORER-HCM and weeks |24 and 96 of MAVA-LTE (data extraction on March 9, (2023). Exploratory end points included left ventricular (LV) mass index, LV maximum wall thickness, volumes land function (left atrial volume maximum index, LV end- diastolic volume index, LV end-sys tolic volume index, and myocardial contractile fraction), focal and diffuse mocar- dial fibrosis (6-SD late gadolinium enhancement [LGE] and average extracellular volume fraction), and LV ejec- tion fraction (LVEF).

CirculationVol. 152(12)
Northwestern University (US), Cedars-Sinai Medical Center (US), Brigham and Women's Hospital (US), Oregon Health & Science University (US), Duke University (US), University of California, San Francisco (US), Owens-Illinois (United States) (US), University of Michigan (US), University of Virginia Health System (US), Tel Aviv Sourasky Medical Center (IL), Yale University (US), NYU Langone Health (US), American Conservatory Theater (US), Meyer Children's Hospital (IT), Hospital da Luz (PT), Kerckhoff Klinik (DE), Bristol-Myers Squibb (Sweden) (SE), Institute of Cardiology (PL), Complexo Hospitalario Universitario A Coruña (ES), Instituto de Investigación Biomédica de A Coruña (ES), University of Virginia (US), University of Göttingen (DE)
Openalex Percentile: Top 15%
Cardiomyopathy and Myosin Studies
1.39
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