Abstract 4147141: Relationship Between CVH and Survival in the Acoramidis Treated Participants Within ATTRibute-CM
Background: Acoramidis is a novel, potent, investigational, transthyretin (TTR) stabilizer under development for the treatment of TTR amyloidosis that results in near-complete (≥90%) TTR stabilization. In a phase 3 study, ATTRibute-CM, acoramidis demonstrated improved clinical outcomes in participants with transthyretin amyloid cardiomyopathy (ATTR-CM), including a 50% reduction in the risk of CVH compared to placebo over 30 months. The study also demonstrated that cardiovascular hospitalization (CVH) during the study predicted a higher subsequent mortality in participants with ATTR-CM. Hypothesis: CVH portends a higher risk of mortality in participants with ATTR-CM. Since acoramidis reduces CVH, it can improve the prognosis of participants with ATTR-CM. Aim: To evaluate the relationship between CVH and survival in the acoramidis group within ATTRibute-CM. Methods: In this post-hoc analysis, the relationship between those with or without CVH and survival was analyzed within the acoramidis treatment group using the Kaplan-Meier (KM) estimator method. Results: Demographics and baseline disease characteristics were mostly comparable between acoramidis-treated participants with and without CVH, although participants with CVH had a higher baseline NT-proBNP and lower eGFR. At Month 30, in acoramidis-treated participants, those without any CVH (n=300) had a higher survival [86.8% (95% CI = 82.2, 90.3)] versus 62.4% (95% CI = 52.6, 70.7) in those who had any CVH (n=109); p<0.0001 from log-rank test (Figure). Conclusion: In the ATTRibute-CM study, pts without any CVH receiving acoramidis have a higher survival rate. CVHs remain a powerful predictor of mortality. This reinforces the importance of an effective therapy that reduces CVH and in turn may improve survival in patients with ATTR-CM.
Authors
- Michael G. Hanna (ORCID: https://orcid.org/0000-0003-0825-4075)
- Keyur B. Shah (ORCID: https://orcid.org/0000-0002-8329-2963)
- Suresh Siddhanti
- Richard Kar-Hang Cheng (ORCID: https://orcid.org/0000-0001-5994-5998)
- Amrut Ambardekar
- Simon Gibbs
- Margot K. Davis (ORCID: https://orcid.org/0000-0001-7367-8267)
- John Whang (ORCID: https://orcid.org/0000-0003-0397-2326)
- José Nativi-Nicolau (ORCID: https://orcid.org/0000-0002-5481-2122)
- Kevin Michael Alexander (ORCID: https://orcid.org/0000-0003-4024-3691)
- Jing Du
- Jean‐François Tamby (ORCID: https://orcid.org/0009-0002-8892-4488)
- Jonathan C. Fox (ORCID: https://orcid.org/0000-0002-1250-5239)
Institutions
- Cleveland Clinic (US)
- University of British Columbia (CA)
- Palo Alto University (US)
- Virginia Commonwealth University (US)
- University of Washington (US)
- Jacksonville College (US)
- WinnMed (US)
- BridgeBio (United States) (US)
- Mayo Clinic in Florida (US)
- Bridge Pharma (United States) (US)
- University of Colorado Anschutz Medical Campus (US)
- University of Colorado Denver (US)
- Stanford University (US)
Publication Details
- Journal
- Circulation
- Published
- 2024-11-12
- DOI
- https://doi.org/10.1161/circ.150.suppl_1.4147141
- Primary Topic
- Anesthesia and Neurotoxicity Research
- Type
- article
- Field-Weighted Citation Impact
- 0.00