Tafamidis in octogenarians with wild-type transthyretin cardiac amyloidosis: an international cohort study.

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Tác giả: Kris Bogaerts, Alexandre Bohyn, Ian Buysschaert, Lars Buytaert, Emma Christiaen, Mathias Claeys, Philippe Debonnaire, Steven Droogmans, Karl Dujardin, Milad El Haddad, Annemie Jacobs, Anne-Catherine Pouleur, René Tavernier, Sander Trenson, Raf Van Hoeyweghen, Nicolas Verheyen, Nicolas Wyseure, David K Zach

Ngôn ngữ: eng

Ký hiệu phân loại: 333.77 Urban lands

Thông tin xuất bản: England : European heart journal , 2025

Mô tả vật lý:

Bộ sưu tập: NCBI

ID: 703357

 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.
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