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               <mods:identifier type="citation">JACC Heart Fail. 2024 Jan;12(1):150-160.</mods:identifier>
               <mods:identifier type="uri">http://hdl.handle.net/20.500.12105/19267</mods:identifier>
               <mods:identifier type="pubmedID">37943223</mods:identifier>
               <mods:identifier type="doi">10.1016/j.jchf.2023.08.032</mods:identifier>
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               <mods:identifier type="journal">JACC. Heart failure</mods:identifier>
               <mods:abstract>BACKGROUND&#xd;
Tafamidis was approved to treat patients with transthyretin amyloid cardiomyopathy (ATTR-CM) on the basis of findings from the phase 3 Tafamidis in Transthyretin Cardiomyopathy Clinical Trial (ATTR-ACT).&#xd;
OBJECTIVES&#xd;
This study was a post hoc analysis exploring tafamidis efficacy in octogenarian patients.&#xd;
METHODS&#xd;
Analysis of patients aged &lt;80 and ≥80 years in ATTR-ACT and its ongoing open-label long-term extension (LTE) study, where all patients receive tafamidis.&#xd;
RESULTS&#xd;
After 30 months in ATTR-ACT, least squares (LS) mean change from baseline in 6-minute walk test (6MWT) distance, N-terminal pro-B-type natriuretic peptide (NT-proBNP) concentration, and Kansas City Cardiomyopathy Questionnaire Overall Summary (KCCQ-OS) score were smaller (all P &lt; 0.05) in patients aged ≥80 years treated with tafamidis (n = 51) vs placebo (n = 37). At the LTE study interim analysis, patients aged ≥80 years treated continuously with tafamidis had a smaller decline in KCCQ-OS score (P &lt; 0.05) and trended toward longer median survival (45 vs 27 months; all-cause mortality HR: 0.6828 [95% CI: 0.4048-1.1517]; P = 0.1526) than those initially treated with placebo in ATTR-ACT. Similar efficacy was observed in patients aged &lt;80 years in ATTR-ACT, including smaller LS mean change from baseline in 6MWT distance, NT-proBNP concentration, and KCCQ-OS score, and lower rate of cardiovascular-related hospitalizations with tafamidis (n = 125) vs placebo (n = 140). In the LTE study, patients aged &lt;80 years treated continuously with tafamidis had a longer median survival (80 vs 41 months; HR = 0.4513 [95% CI: 0.3176-0.6413]; P &lt; 0.0001) and a smaller decline in KCCQ-OS score than those initially treated with placebo.&#xd;
CONCLUSIONS&#xd;
The findings demonstrate tafamidis efficacy for patients with ATTR-CM both in those aged &lt;80 and those aged ≥80 years. (Tafamidis in Transthyretin Cardiomyopathy Clinical Trial [ATTR-ACT]; NCT01994889/Long-term Safety of Tafamidis in Subjects With Transthyretin Cardiomyopathy; NCT02791230).</mods:abstract>
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                  <mods:title>Tafamidis Efficacy Among Octogenarian Patients in the Phase 3 ATTR-ACT and Ongoing Long-Term Extension Study.</mods:title>
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