Abstract 4336093: Effect of Aficamten in Women Compared with Men with Obstructive Hypertrophic Cardiomyopathy

X Xiaowen Wang M Maria Pabon (Cardiovascular Division, Brigham And Women's Hospital, Harvard Medical School, Boston, Massachusetts, 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) B Brian Claggett (Cardiovascular Division, Brigham and Women’s Hospital, Harvard Medical School, Boston) C Caroline Coats (University og Glasgow, Glasgow, United Kingdom) M Martin maron (Lahey Hospital, Burlington, Massachusetts, United States) A Ahmad Masri (Oregon Health and Science University, Portland) B Benjamin Meder (Precision Digital Health, Department of Internal Medicine III, Cardiology, University Heidelberg, Heidelberg, Germany) 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) I Iacopo Olivotto (Department of Cardiology, Meyer Children’s Hospital, IRCCS, Florence, Italy) D Daniel Jacoby (Cytokinetics Inc., South San Francisco, California, United States) S Stephen Heitner (Cytokinetics Inc., South San Francisco, California, United States) A Amy Wohltman (Cytokinetics, South San Francisco, CA) S Scott Solomon (Brigham and Women's Hospital, Boston, Massachusetts, United States) S Sheila Hegde (The University of Texas Southwestern Medical Center, Dallas, Texas, United States)

Abstract

Background: Women with obstructive hypertrophic cardiomyopathy (oHCM) may present with a greater burden of disease and carry a worse prognosis. Whether there are sex-related differences in response to aficamten is unknown. Research Question: To assess the change in clinical and echocardiographic characteristics in response to aficamten in male and female participants of the SEQUOIA-HCM trial. Methods: A post-hoc analysis of sex differences in the double-blind, randomized-controlled SEQUOIA-HCM trial of aficamten versus placebo in patients with oHCM was performed. Baseline clinical and echocardiographic characteristics were compared using t-test for continuous variables and C 2 test for categorical variables. Prespecified primary (change in peak oxygen uptake, pVO 2 ) and secondary endpoints from baseline to end of treatment (week 24) were analyzed using linear regression models, adjusted for baseline values, beta-blocker use, and exercise mode. Results: Of the 282 participants in SEQUOIA-HCM, women (n=115, 41%) were older, had lower Kansas City Cardiomyopathy Questionnaire (KCCQ) scores, higher NT-proBNP levels, and lower pVO 2 at baseline (Table 1). Women had smaller left ventricular (LV) chamber sizes, higher E/e’ ratios, and higher LV outflow tract (LVOT) gradients at rest and with Valsalva. At 24 weeks, there was a significant treatment-related increase in pVO 2 in men (+2.0 [+0.9 to +3.0]) and women (+1.5, [+0.7 to +2.4]), with no significant interaction by sex (p-interaction = 0.51). Both men and women had a significant treatment-related decrease in LVOT gradients at rest and with Valsalva (Figure 1) with no sex-by-treatment interaction (p-interaction ≥ 0.13). Women had a trend towards greater improvement in KCCQ-CSS (Table 1, p-interaction = 0.08) and a greater reduction in lateral E/e’ ratio (Figure 1, p-interaction = 0.01). Women had similar geometric mean proportional reduction in NT-proBNP (women: 0.16 [0.13 to 0.21]; men: 0.22 [0.18 to 0.27], P-interaction = 0.10). Conclusions: Women enrolled in SEQUOIA-HCM were older with worse baseline health status, higher NT-proBNP, higher LV filling pressure, and higher LVOT gradients compared to men. Despite these differences, both men and women derived similar benefits in the primary and most secondary endpoints following treatment with aficamten, with a greater improvement in health status in women.

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 (16)

X

Xiaowen Wang

M

Maria Pabon

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

B

Brian Claggett

Cardiovascular Division, Brigham and Women’s Hospital, Harvard Medical School, Boston

C

Caroline Coats

University og Glasgow, Glasgow, United Kingdom

M

Martin maron

Lahey Hospital, Burlington, Massachusetts, United States

A

Ahmad Masri

Oregon Health and Science University, Portland

B

Benjamin Meder

Precision Digital Health, Department of Internal Medicine III, Cardiology, University Heidelberg, Heidelberg, Germany

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

I

Iacopo Olivotto

Department of Cardiology, Meyer Children’s Hospital, IRCCS, Florence, Italy

D

Daniel Jacoby

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

S

Stephen Heitner

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

A

Amy Wohltman

Cytokinetics, South San Francisco, CA

S

Scott Solomon

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

S

Sheila Hegde

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