Clinical outcomes for 2788 patients with transthyretin amyloidosis: Tafamidis meglumine early access program in France.

France Heart failure Real-world data Tafamidis Transthyretin cardiac amyloidosis

Journal

Archives of cardiovascular diseases
ISSN: 1875-2128
Titre abrégé: Arch Cardiovasc Dis
Pays: Netherlands
ID NLM: 101465655

Informations de publication

Date de publication:
05 Oct 2024
Historique:
received: 06 03 2024
revised: 20 08 2024
accepted: 26 08 2024
medline: 20 10 2024
pubmed: 20 10 2024
entrez: 19 10 2024
Statut: aheadofprint

Résumé

Early access experience in France with tafamidis meglumine, a selective transthyretin stabilizer for transthyretin-related amyloidosis cardiomyopathy (ATTR-CM), following transthyretin-related amyloidosis (ATTR) polyneuropathy approval and positive ATTR-ACT study results. To describe the characteristics and clinical outcomes for patients in the French ATTR-CM tafamidis meglumine early access programme (28 Nov 2018 to 01 Jun 2021). Patients with confirmed ATTR-CM received tafamidis meglumine 20mg/day or 80mg/day. Demographic and clinical data were collected prospectively until patients discontinued treatment or died, or the programme ended. Overall, 222 physicians from 126 centres enrolled 2788 patients. The median age was 82years, 81.6% were male and New York Heart Association severity was class I for 12.8%, class II for 60.1% and class III for 27.0%. Overall, 1943 (74.6%) had genetic testing, and the results were available at tafamidis start for 1208 (62.2%) patients: 995 (82.4%) had wild-type ATTR and 213 (17.6%) had hereditary ATTR. Most patients started treatment≤12months after diagnosis (88.3%): 2268 (81.3%) at 20mg/day, with 401 (17.7%) increasing to 80mg/day. Median follow-up duration was 11.8months. New York Heart Association class improved or remained stable for 1299 (77.6%), whereas 376 (22.4%) worsened between inclusion and last follow-up. Among patients initiated at 80mg, 297 (81.1%) improved or remained stable and 69 (18.9%) worsened. New York Heart Association class progression did not vary with age. The 18-month survival rates were 89.8% (95% confidence interval: 87.0-92.0) among patients aged<80years, and 86.5% (95% confidence interval: 83.9-88.7) among those aged≥80years. Early tafamidis meglumine access was given to 2788 patients with ATTR-CM. New York Heart Association class progression and survival were consistent with previously published data.

Sections du résumé

BACKGROUND BACKGROUND
Early access experience in France with tafamidis meglumine, a selective transthyretin stabilizer for transthyretin-related amyloidosis cardiomyopathy (ATTR-CM), following transthyretin-related amyloidosis (ATTR) polyneuropathy approval and positive ATTR-ACT study results.
AIM OBJECTIVE
To describe the characteristics and clinical outcomes for patients in the French ATTR-CM tafamidis meglumine early access programme (28 Nov 2018 to 01 Jun 2021).
METHODS METHODS
Patients with confirmed ATTR-CM received tafamidis meglumine 20mg/day or 80mg/day. Demographic and clinical data were collected prospectively until patients discontinued treatment or died, or the programme ended.
RESULTS RESULTS
Overall, 222 physicians from 126 centres enrolled 2788 patients. The median age was 82years, 81.6% were male and New York Heart Association severity was class I for 12.8%, class II for 60.1% and class III for 27.0%. Overall, 1943 (74.6%) had genetic testing, and the results were available at tafamidis start for 1208 (62.2%) patients: 995 (82.4%) had wild-type ATTR and 213 (17.6%) had hereditary ATTR. Most patients started treatment≤12months after diagnosis (88.3%): 2268 (81.3%) at 20mg/day, with 401 (17.7%) increasing to 80mg/day. Median follow-up duration was 11.8months. New York Heart Association class improved or remained stable for 1299 (77.6%), whereas 376 (22.4%) worsened between inclusion and last follow-up. Among patients initiated at 80mg, 297 (81.1%) improved or remained stable and 69 (18.9%) worsened. New York Heart Association class progression did not vary with age. The 18-month survival rates were 89.8% (95% confidence interval: 87.0-92.0) among patients aged<80years, and 86.5% (95% confidence interval: 83.9-88.7) among those aged≥80years.
CONCLUSIONS CONCLUSIONS
Early tafamidis meglumine access was given to 2788 patients with ATTR-CM. New York Heart Association class progression and survival were consistent with previously published data.

Identifiants

pubmed: 39426850
pii: S1875-2136(24)00323-1
doi: 10.1016/j.acvd.2024.08.006
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024. Published by Elsevier Masson SAS.

Auteurs

Olivier Lairez (O)

Cardiac Imaging Centre, Department of Cardiology, Toulouse University Hospital, 31059 Toulouse, France.

Patricia Réant (P)

Cardiology Department, Haut-Levêque Hospital, Bordeaux University Hospital, University of Bordeaux, Inserm 1045, IHU Lyric, CIC1401, 33600 Pessac, France.

Jocelyn Inamo (J)

Reception Team 7525, Cardiology Department, Hospital P. Zobda-Quitman, Martinique University Hospital, University of Antilles, 97261 Fort-de-France, Martinique.

Julian Jeanneteau (J)

Cardiology, Clinique Saint-Joseph, 49800 Trelazé, France.

Fabrice Bauer (F)

Department of Cardiac Surgery, Rouen University Hospital, Normandy University, UNIROUEN, Inserm U1096, 76000 Rouen, France.

Gilbert Habib (G)

Cardiology Department, La Timone University Hospital, 13005 Marseille, France.

Jean-Christophe Eicher (JC)

Cardiology Department, François-Mittérrand Hospital, Dijon University Hospital, 21000 Dijon, France.

Benoit Lequeux (B)

Cardiology Department, Poitiers University Hospital, 86000 Poitiers, France.

Damien Legallois (D)

Normandy University, UNICAEN, Inserm U1086 ANTICIPE, 14000 Caen, France.

Constant Josse (C)

eXYSTAT, 92240 Malakoff, France.

Aurelie Hippocrate (A)

Pfizer, 75014 Paris, France.

Mathilde Bartoli (M)

Pfizer, 75014 Paris, France.

Margaux Dubois (M)

Pfizer, 75014 Paris, France.

Charlotte Noirot Cosson (C)

Pfizer, 75014 Paris, France.

Pierre-Alexandre Squara (PA)

Pfizer, 75014 Paris, France.

Stephane Fievez (S)

Pfizer, 75014 Paris, France.

Aurore Quinault (A)

Pfizer, 75014 Paris, France.

Jeremie Rudant (J)

Pfizer, 75014 Paris, France.

Mounira Kharoubi (M)

Cardiology Department and French National Reference Centre for Cardiac Amyloidosis, Henri-Mondor University Hospital, AP-HP, GRC Amyloid Research Institute and IMRB, Inserm, Université Paris Est Créteil, 94010 Créteil, France.

Thibaud Damy (T)

Cardiology Department and French National Reference Centre for Cardiac Amyloidosis, Henri-Mondor University Hospital, AP-HP, GRC Amyloid Research Institute and IMRB, Inserm, Université Paris Est Créteil, 94010 Créteil, France. Electronic address: thibaud.damy@aphp.fr.

Classifications MeSH