Abstract 4365842: Chronic Aficamten Treatment Results in Sustained Favorable Cardiac Remodeling in Patients with Symptomatic Obstructive Hypertrophic Cardiomyopathy: Insights From the FOREST-HCM Trial
Abstract
Background: Aficamten treatment over 24 weeks in SEQUOIA-HCM (NCT05186818) improved left ventricular (LV) outflow tract gradients (LVOT-G), showed evidence of favorable cardiac remodeling, and improved measures of LV diastolic function in patients with obstructive hypertrophic cardiomyopathy (oHCM). Whether longer-term treatment over 48 weeks results in further cardiac remodeling is unknown. Research Question: This study evaluates the effect of chronic treatment with aficamten on echocardiographic measures of cardiac structure and function in FOREST-HCM (NCT04848506), an open-label extension study that enrolled patients who completed a parent study with aficamten. Methods: Serial echocardiograms were performed in patients receiving open-label aficamten (5–20 mg daily) titrated to relieve LVOT obstruction (Valsalva LVOT <30 mmHg) while maintaining LV ejection fraction (LVEF) 50%. Results: As of August 31, 2024, 169 patients (mean±SD age 60±13 years; 45.6% female, 95.6% White, 2.4% Black, 1.2% Asian) completed 48 weeks of follow-up. Aficamten treatment resulted in sustained improvement in Valsalva and resting LVOT-G, LV wall thickness, left atrial volume index, and lateral and septal E/e' ( Figure 1 ). LVEF decreased mildly (-7±8%) and remained stable within a normal range between weeks 24 and 48. After 48 weeks, 74 patients demonstrated improvement in the total number of normal LV diastolic function measures ( Figure 2 ). Conclusion: Treatment with aficamten for 48 weeks in patients with oHCM resulted in significant improvement in important measures of cardiac structure and function, with continued benefit after 24 weeks and no meaningful adverse effects on LV systolic function, indicating sustained and favorable long-term cardiac remodeling.
Article Details
Authors (22)
Sheila Hegde
The University of Texas Southwestern Medical Center, Dallas, Texas, United States
Maria Pabon
Cardiovascular Division, Brigham And Women's Hospital, Harvard Medical School, Boston, Massachusetts, United States
Ahmad Masri
Oregon Health and Science University, Portland
Michael Nassif
University of Missouri Kansas City Healthcare Institute for Innovations in Quality and Saint Luke’s Mid America Heart Institute, Kansas City, Missouri, United States
Theodore Abraham
Department of Cardiology, University of, California, San Francisco, San Francisco
Roberto Barriales-Villa
Complexo Hospitalario Universitario A Coruña, Instituto de Investigación Biomédica de A Coruña, CIBERCV–Instituto de Salud Carlos III, A Coruña, Spain
Robert Cooper
Liverpool Heart and Chest Hospital, Liverpool, United Kingdom
Perry Elliott
Institute of Cardiovascular Science, University College, London
Martin maron
Lahey Hospital, Burlington, Massachusetts, United States
Artur Oreziak
National Institute of Cardiology, Warsaw, Poland
Anjali Owens
Albree Tower Rader
Massachusetts General Hospital, Boston, Massachusetts, United States
Stephen Heitner
Cytokinetics Inc., South San Francisco, California, United States
Daniel Jacoby
Cytokinetics Inc., South San Francisco, California, United States
Stuart Kupfer
Cytokinetics, South San Francisco, CA
Xueli Liu
Fady Malik
Cytokinetics Inc., South San Francisco, California, United States
Chiara Melloni
Cytokinetics Inc., South San Francisco, California, United States
Tyrell Simkins
Jenny Wei
Cytokinetics Inc., South San Francisco, California, United States
Scott Solomon
Brigham and Women's Hospital, Boston, Massachusetts, United States
Sara Saberi