Real-world multidisciplinary outcomes of onasemnogene abeparvovec monotherapy in patients with spinal muscular atrophy type 1: experience of the French cohort in the first three years of treatment

Our study shows favorable motor outcomes and preserved respiratory and feeding functions in treatment-naive SMA1 infants treated by GT as the first and only therapy before respiratory and bulbar dysfunctions occurred. Nevertheless, almost all patients developed spinal deformities.

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Publication Details

Journal
Orphanet Journal of Rare Diseases
Published
2024-09-13
DOI
https://doi.org/10.1186/s13023-024-03326-3
Citations
14
Primary Topic
Neurogenetic and Muscular Disorders Research
Type
article
Field-Weighted Citation Impact
6.13

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article

Real-world multidisciplinary outcomes of onasemnogene abeparvovec monotherapy in patients with spinal muscular atrophy type 1: experience of the French cohort in the first three years of treatment

Cyril Schweitzer, Rémi Barrois, Catherine Sarret, Christian Richelme et al.
14 citations
Orphanet Journal of Rare Diseases
Neurogenetic and Muscular Disorders Research
6.13
article

Real-world multidisciplinary outcomes of onasemnogene abeparvovec monotherapy in patients with spinal muscular atrophy type 1: experience of the French cohort in the first three years of treatment

Cyril Schweitzer, Rémi Barrois, Catherine Sarret, Christian Richelme, C. Cancès, Susana Quijano‐Roy, Isabelle Desguerre, Vincent Laugel, J. Durigneux, Marine Guichard, Marta Gómez‐García de la Banda, Cécilia Altuzarra, B. Chabrol, Caroline Espil‐Taris, Laure Le Goff, Arnaud Isapof, Mondher Chouchane, Christine Barnérias, Frédérique Audic, Ulrike Walther‐Louvier, Valérie Trommsdorff, Marie Thibaud, Hervé Testard, Catherine Vanhulle, Sandra Mercier, Anne Pervillé, Juliette Ropars, Jean Baptiste Davion, Macarena Nougues
article en
14 citations

Abstract

Our study shows favorable motor outcomes and preserved respiratory and feeding functions in treatment-naive SMA1 infants treated by GT as the first and only therapy before respiratory and bulbar dysfunctions occurred. Nevertheless, almost all patients developed spinal deformities.

Orphanet Journal of Rare DiseasesVol. 19(1)
Hôpital Necker-Enfants Malades (FR), Inserm (FR), Université de Versailles Saint-Quentin-en-Yvelines (FR), Université Paris-Saclay (FR), Centre Hospitalier Universitaire de Grenoble (FR), Sorbonne Université (FR), Hôpital Femme Mère Enfant (FR), Hôpital Armand-Trousseau (FR), Centre Hospitalier Universitaire de La Réunion (RE), Centre Hospitalier Universitaire de Besançon (FR), Hôpital Charles-Nicolle (FR), Hôpital Couple Enfant (FR), Centre Hospitalier Universitaire de Tours (FR), Assistance Publique – Hôpitaux de Paris (FR), Centre Hospitalier Régional et Universitaire de Nancy (FR), Hôpital d'Enfants (FR), Centre Hospitalier Universitaire de Reims (FR), Hôpital Gui de Chauliac (FR), Hôpital Pellegrin (FR), Centre Hospitalier Universitaire de Clermont-Ferrand (FR), Hôpital Avicenne (FR), Centre Oscar Lambret (FR), Centre Hospitalier Régional Universitaire de Brest (FR), Hôpital Raymond-Poincaré (FR), Fondation Lenval (FR), Maison des Sciences sociales et des Humanités de Dijon (FR), Hôpital des Enfants (FR), Hôpital d'Hautepierre (FR), Hôpital de la Timone (FR), Institut des Maladies Génétiques Imagine (FR), Université d'Angers (FR), Université de Rouen Normandie (FR), Université Grenoble Alpes (FR), Université de Reims Champagne-Ardenne (FR), Nantes Université (FR)
Agence Nationale de Sécurité du Médicament et des Produits de Santé
Good health and well-being
Openalex Percentile: Top 3%
Neurogenetic and Muscular Disorders Research
6.13
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