One-year real-world experience with mavacamten and its physiologic effects on obstructive hypertrophic cardiomyopathy

Mavacamten is a first-in-class cardiac myosin ATPase inhibitor, approved by the United States Food and Drug Administration for the treatment of hypertrophic cardiomyopathy with obstructive physiology (oHCM). Here, we present the real-world use of mavacamten in 50 patients with oHCM at a tertiary care referral center. In both our highlighted case and in our aggregate data, we report significant improvement in wall thickness, mitral regurgitation, left ventricular outflow tract obstruction and New York Heart Association symptom class. Moreover, in our center's experience, neither arrhythmia burden, nor contractility have worsened in the vast majority of patients: we note a clinically insignificant mean decrease in left ventricular ejection fraction (LVEF), with only two patients requiring temporary mavacamten discontinuance for LVEF < 50%. Adverse events were rare, unrelated to mavacamten itself, and seen solely in patients with disease too advanced to have been represented in clinical trials. Moreover, our multidisciplinary pathway enabled us to provide a large number of patients with a novel closely-monitored therapeutic within just a few months of commercial availability. These data lead us to conclude that mavacamten, as a first-in-class cardiac myosin inhibitor, is safe and efficacious in real-world settings.

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Publication Details

Journal
Frontiers in Cardiovascular Medicine
Published
2024-08-30
DOI
https://doi.org/10.3389/fcvm.2024.1429230
Citations
16
Primary Topic
Cardiomyopathy and Myosin Studies
Type
article
Field-Weighted Citation Impact
6.43

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article

One-year real-world experience with mavacamten and its physiologic effects on obstructive hypertrophic cardiomyopathy

Emily Keamy-Minor, Daniel Seung Kim, Joshua W. Knowles, Colleen Bonnett et al.
16 citations
Frontiers in Cardiovascular Medicine
Cardiomyopathy and Myosin Studies
6.43
article

One-year real-world experience with mavacamten and its physiologic effects on obstructive hypertrophic cardiomyopathy

Emily Keamy-Minor, Daniel Seung Kim, Joshua W. Knowles, Colleen Bonnett, Isabella Cuenco, Heidi Salisbury, Michael B. Liu, Victoria Nicole Parikh, Matthew T. Wheeler, Karim Sallam, Jack W. O’Sullivan, Marco Valentin Perez, Masataka Kawana, Euan Angus Ashley, Andrea Linder, Allysonne Smith, Chad S. Weldy, Yaanik Desai, Ellen Bacolor, Kathleen Lacar, Elise Munsey, Nancy Robles, Ishan Paranjpe, Cindy Lamendola, Beth Kao, Emily L. Chu, Wilson L. Tang, Kimberly Hecker
article en
16 citations

Abstract

Mavacamten is a first-in-class cardiac myosin ATPase inhibitor, approved by the United States Food and Drug Administration for the treatment of hypertrophic cardiomyopathy with obstructive physiology (oHCM). Here, we present the real-world use of mavacamten in 50 patients with oHCM at a tertiary care referral center. In both our highlighted case and in our aggregate data, we report significant improvement in wall thickness, mitral regurgitation, left ventricular outflow tract obstruction and New York Heart Association symptom class. Moreover, in our center's experience, neither arrhythmia burden, nor contractility have worsened in the vast majority of patients: we note a clinically insignificant mean decrease in left ventricular ejection fraction (LVEF), with only two patients requiring temporary mavacamten discontinuance for LVEF < 50%. Adverse events were rare, unrelated to mavacamten itself, and seen solely in patients with disease too advanced to have been represented in clinical trials. Moreover, our multidisciplinary pathway enabled us to provide a large number of patients with a novel closely-monitored therapeutic within just a few months of commercial availability. These data lead us to conclude that mavacamten, as a first-in-class cardiac myosin inhibitor, is safe and efficacious in real-world settings.

Frontiers in Cardiovascular MedicineVol. 11
Cardiovascular Institute of the South (US), Stanford University (US)
American Heart Association, Bristol-Myers Squibb, AstraZeneca, Sarnoff Cardiovascular Research Foundation, National Institutes of Health, National Heart, Lung, and Blood Institute
Openalex Percentile: Top 3%
Cardiomyopathy and Myosin Studies
6.43
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