Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/45689
Title: Tafamidis in octogenarians with wild-type transthyretin cardiac amyloidosis: an international cohort study
Authors: Debonnaire, Philippe
Dujardin, Karl
Verheyen, Nicolas
Pouleur, Anne-Catherine
Droogmans, Steven
Claeys, Mathias
Bohyn, Alexandre
BOGAERTS, Kris 
El Haddad, Milad
Christiaen, Emma
Wyseure, Nicolas
Zach, David K.
Buytaert, Lars
Jacobs , Annemie
Buysschaert, Ian
Trenson, Sander
Van Hoeyweghen, Raf
Tavernier, Rene
Issue Date: 2025
Publisher: OXFORD UNIV PRESS
Source: European heart journal, 46 (11) , p. 1057 -1070
Abstract: Background and Aims In real-world, wild-type transthyretin cardiomyopathy is increasingly diagnosed in patients >= 80 years old (octogenarians), although being underrepresented in randomized clinical trials. Specific data on natural course and outcome under tafamidis treatment in octogenarians are therefore scarce. The impact of tafamidis treatment on mortality in real-world wild-type transthyretin cardiomyopathy octogenarians was studied. Methods An international, multicentre cohort study of 710 consecutive wild-type transthyretin cardiomyopathy patients with mean follow-up of 2.2 +/- 1.8 years for all-cause mortality endpoint was performed. Results The cohort consisted of 58.5% (415/710) octogenarians (85 +/- 4 years, 74.2% male). Before tafamidis availability, natural course in octogenarians (148/257) vs. non-octogenarians (109/257) was poor, with 16% 1-year and 71% 5-year mortality vs. 8% and 47%, respectively (P < .001). Since tafamidis availability, 70.1% (253/361) octogenarians were initiated on tafamidis vs. 83.7% (231/276) non-octogenarians (P < .001). Tafamidis discontinuation was similar (octogenarians 10.3% and non-octogenarians 7.4%; P = .260). Overall tafamidis treated vs. untreated octogenarians had better unadjusted survival (P < .001), with 5% 1-year and 24% 3-year mortality. Tafamidis treatment associated with lower mortality after propensity score matching on baseline variables, including age, National Amyloidosis Centre stage, and New York Heart Association class in on average 394 subjects [hazard ratio (HR) = 0.53, 95% confidence interval (CI) 0.34-0.84, P = .007], also in octogenarians (HR = 0.57, 95% CI 0.33-1.01, P = .053). Neither age at diagnosis (P = .217) nor at treatment initiation (P = .154) interacted with tafamidis mortality benefit. Octogenarians had poorer survival despite tafamidis, when initiated at >= 90 years (HR = 3.3, 95% CI 1.10-9.53, P = .033) and National Amyloidosis Centre Stage >= 3 (HR = 2.4, 95% CI 0.87-6.46, P = .090). Conclusions Real-world tafamidis treatment improves survival without age affecting treatment efficacy, although mortality remains considerable in octogenarians.
Notes: Debonnaire, P (corresponding author), AZ Sint Jan Brugge, Dept Cardiol, Ruddershove 10, B-8000 Brugge, Belgium.
philippe.debonnaire@azsintjan.be
Keywords: Octogenarian;Tafamidis;Transthyretin;Cardiac amyloidosis;Cardiomyopathy;Mortality
Document URI: http://hdl.handle.net/1942/45689
ISSN: 0195-668X
e-ISSN: 1522-9645
DOI: 10.1093/eurheartj/ehae923
ISI #: 001437274900001
Rights: The Author(s) 2025. Published by Oxford University Press on behalf of the European Society of Cardiology. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
Category: A1
Type: Journal Contribution
Appears in Collections:Research publications

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