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Tafamidis Efficacy Among Octogenarian Patients in the Phase 3 ATTR-ACT and Ongoing Long-Term Extension Study.
Garcia-Pavia, Pablo; Sultan, Marla B; Gundapaneni, Balarama; Sekijima, Yoshiki; Perfetto, Federico; Hanna, Mazen; Witteles, Ronald.
Afiliação
  • Garcia-Pavia P; Hospital Universitario Puerta de Hierro Majadahonda, IDIPHISA, CIBERCV, Madrid, Spain; Centro Nacional de Investigaciones Cardiovasculares (CNIC), Madrid, Spain; Universidad Francisco de Vitoria (UFV), Pozuelo de Alarcón, Madrid, Spain. Electronic address: pablogpavia@yahoo.es.
  • Sultan MB; Pfizer Inc, New York, New York, USA.
  • Gundapaneni B; Pfizer Inc, Groton, Connecticut, USA.
  • Sekijima Y; Department of Medicine (Neurology and Rheumatology), Shinshu University School of Medicine, Matsumoto, Japan.
  • Perfetto F; Tuscan Regional Amyloid Referral Centre, Careggi University Hospital, Florence, Italy.
  • Hanna M; Department of Cardiovascular Medicine, Cleveland Clinic, Cleveland, Ohio, USA.
  • Witteles R; Stanford University School of Medicine, Stanford, California, USA.
JACC Heart Fail ; 12(1): 150-160, 2024 Jan.
Article em En | MEDLINE | ID: mdl-37943223
ABSTRACT

BACKGROUND:

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).

OBJECTIVES:

This study was a post hoc analysis exploring tafamidis efficacy in octogenarian patients.

METHODS:

Analysis of patients aged <80 and ≥80 years in ATTR-ACT and its ongoing open-label long-term extension (LTE) study, where all patients receive tafamidis.

RESULTS:

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 < 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 < 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 <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 <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 < 0.0001) and a smaller decline in KCCQ-OS score than those initially treated with placebo.

CONCLUSIONS:

The findings demonstrate tafamidis efficacy for patients with ATTR-CM both in those aged <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).
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neuropatias Amiloides Familiares / Insuficiência Cardíaca / Cardiomiopatias Limite: Aged / Aged80 / Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neuropatias Amiloides Familiares / Insuficiência Cardíaca / Cardiomiopatias Limite: Aged / Aged80 / Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article