Abstract 4365761: Acoramidis Lowers NT-proBNP in a Larger Proportion of ATTRibute-CM Study Participants With Transthyretin Amyloid Cardiomyopathy Compared with Placebo, Independent of Atrial Fibrillation Status
Abstract
Background: Atrial fibrillation/flutter (AF/AFL) is a frequent complication of heart failure in transthyretin amyloid cardiomyopathy (ATTR-CM) and its increasing incidence is a marker of disease progression. Increasing N-terminal B-type natriuretic peptide (NT-proBNP) levels are also an independent indicator of ATTR-CM progression and higher NT-proBNP levels are seen in ATTR-CM with superimposed AF. Acoramidis achieves near-complete (≥90%) TTR stabilization, and is approved in the USA, UK, Europe and Japan for the treatment of ATTR-CM in adults. Acoramidis blunts the progressive rise in NT-proBNP, compared with placebo in patients with ATTR-CM. Research Question: How does acoramidis treatment influence ATTR-CM disease progression based on NT-proBNP levels in the presence or absence of AF/AFL? Methods: The ATTRibute-CM (NCT03860935) study has been published. This post hoc analysis was conducted in the modified intention-to-treat population who had baseline (BL) and Month 30 NT-proBNP assessments (n=413). Categories defined were: 1) presence or absence of AF/AFL diagnosis at BL (defined as recorded AF medical history or presence of AF/AFL on ECG at enrollment), 2) incidence of AF/AFL treatment-emergent adverse event (TEAE) during the study, and 3) AF/AFL at any time (defined as [1] or [2]). Clinically meaningful improvement at Month 30 was defined as a reduction of >300 pg/mL and >30% in NT-proBNP from BL. AF/AFL TEAEs were identified using ‘atrial fibrillation’, ‘atrial flutter’ and ‘cardiac flutter’ MedDRA preferred terms. Results: At study entry, participants with BL AF/AFL had lower 6-minute walk distances, left ventricular ejection fractions and Kansas City Cardiomyopathy Questionnaire Overall Summary scores, higher NT-proBNP levels and were more frequently categorized in higher National Amyloidosis Centre stages versus those without BL AF/AFL. Other BL characteristics were comparable between groups. At Month 30, a higher proportion of participants had improved NT-proBNP with acoramidis than with placebo, regardless of AF/AFL status at BL and/or development of AF/AFL during the study ( Table ). Conclusions: In ATTRibute-CM, the proportion of participants with improved NT-proBNP at Month 30 was consistently around 15 percentage points higher with acoramidis than placebo, regardless of AF/AFL status at BL or during the study. The ongoing open-label extension study may offer insights into the durability of this effect and its long-term clinical consequences.
Article Details
Authors (15)
Mathew Maurer
Columbia University, New York, New York, United States
Kevin Alexander
Division of Cardiovascular Medicine, Department of Medicine, Stanford Center for Clinical Research, Stanford University School of Medicine, Palo Alto, California, United States
Laura Obici
Fondazione IRCCS Policlinico San Matteo, Pavia, Italy
Steen Poulsen
Aarhus University Hospital, Aarhus, Denmark
James Januzzi
Baim Institute for Clinical Research, Boston, Massachusetts, United States
Ronald Witteles
Stanford University, Stanford, California, United States
Wael Jaber
Cleveland Clinic Coordinating Center for Clinical Research, Heart Vascular Thoracic Institute, Cleveland Clinic, Cleveland
Yevgeniy Brailovsky
Columbia University Irving Medical Center, New York, New York, United States
Kai Vogtlaender
Bayer AG, Wuppertal, Germany
Adam Castano
BridgeBio Pharma, Inc., San Francisco, California, United States
Jean-Francois Tamby
BridgeBio Pharma, Inc., San Francisco, California, United States
Jonathan Fox
BridgeBio Pharma, Inc., San Francisco, California, United States
Sumeet Mitter
Inova Schar Heart and Vascular, Falls Church, Virginia, United States
Mazen Hanna
Department of Cardiovascular Medicine, Heart, Vascular & Thoracic Institute, Cleveland Clinic, OH.
Brett Sperry
Saint Luke’s Mid America Heart Institute and the University of Missouri-Kansas City, Kansas City, Missouri, United States