Abstract 4365842: Chronic Aficamten Treatment Results in Sustained Favorable Cardiac Remodeling in Patients with Symptomatic Obstructive Hypertrophic Cardiomyopathy: Insights From the FOREST-HCM Trial

S Sheila Hegde (The University of Texas Southwestern Medical Center, Dallas, Texas, United States) M Maria Pabon (Cardiovascular Division, Brigham And Women's Hospital, Harvard Medical School, Boston, Massachusetts, United States) A Ahmad Masri (Oregon Health and Science University, Portland) M 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) T Theodore Abraham (Department of Cardiology, University of, California, San Francisco, San Francisco) R Roberto Barriales-Villa (Complexo Hospitalario Universitario A Coruña, Instituto de Investigación Biomédica de A Coruña, CIBERCV–Instituto de Salud Carlos III, A Coruña, Spain) R Robert Cooper (Liverpool Heart and Chest Hospital, Liverpool, United Kingdom) P Perry Elliott (Institute of Cardiovascular Science, University College, London) M Martin maron (Lahey Hospital, Burlington, Massachusetts, United States) A Artur Oreziak (National Institute of Cardiology, Warsaw, Poland) A Anjali Owens A Albree Tower Rader (Massachusetts General Hospital, Boston, Massachusetts, United States) S Stephen Heitner (Cytokinetics Inc., South San Francisco, California, United States) D Daniel Jacoby (Cytokinetics Inc., South San Francisco, California, United States) S Stuart Kupfer (Cytokinetics, South San Francisco, CA) X Xueli Liu F Fady Malik (Cytokinetics Inc., South San Francisco, California, United States) C Chiara Melloni (Cytokinetics Inc., South San Francisco, California, United States) T Tyrell Simkins J Jenny Wei (Cytokinetics Inc., South San Francisco, California, United States) S Scott Solomon (Brigham and Women's Hospital, Boston, Massachusetts, United States) S Sara Saberi

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

Journal Circulation
Volume / Issue Vol. 152, Issue Suppl_3
Published November 04, 2025
ISSN 0009-7322
Publisher Lippincott Williams & Wilkins

Journal Info

Circulation

Lippincott Williams & Wilkins

ISSN: 0009-7322 Health Sciences

Authors (22)

S

Sheila Hegde

The University of Texas Southwestern Medical Center, Dallas, Texas, United States

M

Maria Pabon

Cardiovascular Division, Brigham And Women's Hospital, Harvard Medical School, Boston, Massachusetts, United States

A

Ahmad Masri

Oregon Health and Science University, Portland

M

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

T

Theodore Abraham

Department of Cardiology, University of, California, San Francisco, San Francisco

R

Roberto Barriales-Villa

Complexo Hospitalario Universitario A Coruña, Instituto de Investigación Biomédica de A Coruña, CIBERCV–Instituto de Salud Carlos III, A Coruña, Spain

R

Robert Cooper

Liverpool Heart and Chest Hospital, Liverpool, United Kingdom

P

Perry Elliott

Institute of Cardiovascular Science, University College, London

M

Martin maron

Lahey Hospital, Burlington, Massachusetts, United States

A

Artur Oreziak

National Institute of Cardiology, Warsaw, Poland

A

Anjali Owens

A

Albree Tower Rader

Massachusetts General Hospital, Boston, Massachusetts, United States

S

Stephen Heitner

Cytokinetics Inc., South San Francisco, California, United States

D

Daniel Jacoby

Cytokinetics Inc., South San Francisco, California, United States

S

Stuart Kupfer

Cytokinetics, South San Francisco, CA

X

Xueli Liu

F

Fady Malik

Cytokinetics Inc., South San Francisco, California, United States

C

Chiara Melloni

Cytokinetics Inc., South San Francisco, California, United States

T

Tyrell Simkins

J

Jenny Wei

Cytokinetics Inc., South San Francisco, California, United States

S

Scott Solomon

Brigham and Women's Hospital, Boston, Massachusetts, United States

S

Sara Saberi