TY - JOUR
T1 - Respiratory outcomes of onasemnogene abeparvovec treatment for spinal muscular atrophy
T2 - national real-world cohort study
AU - Lavie, Moran
AU - Rochman, Mika
AU - Armoni Domany, Keren
AU - Golan Tripto, Inbal
AU - Be’er, Moria
AU - Besor, Omri
AU - Sagi, Liora
AU - Aharoni, Sharon
AU - Ginsberg, Mira
AU - Noyman, Iris
AU - Levine, Hagit
N1 - Publisher Copyright:
© The Author(s) 2024.
PY - 2025/1/1
Y1 - 2025/1/1
N2 - Onasemnogene abeparvovec (OA) is a novel gene replacement therapy for patients with spinal muscular atrophy (SMA). This study provides real-world respiratory data for pediatric SMA patients receiving OA who were assessed before and one year after treatment in a multicenter cohort study conducted from 2019 to 2021. Twenty-five OA-treated SMA patients (23 with type 1 and 2 with type 2; median age at treatment 6.1 months, with a range of 0.36–23 months) were included. Sixteen were treatment-naïve, and nine had received various prior treatments. Two patients died due to respiratory failure during the study period. Of the remaining 23 patients, four were put on non-invasive ventilation (NIV), bringing ventilated patients to a total of ten during the post-treatment year. Three patients required permanent NIV support, while 13 did not require any respiratory support. Ventilation time decreased from 14.3 to 11.1 hours per day, and respiratory hospitalizations decreased by 26% (from 0.76 to 0.57 per life year). Fifteen of the 23 patients maintained full oral nutrition at study closure compared to 20 of the 25 at study initiation. This real-world data analysis demonstrates that OA may improve respiratory outcomes in SMA patients. Importantly, compounding factors, such as age at treatment initiation, treatment combinations, and natural history, may influence the respiratory course, thus highlighting the need for standardized long-term management. (Table presented.)
AB - Onasemnogene abeparvovec (OA) is a novel gene replacement therapy for patients with spinal muscular atrophy (SMA). This study provides real-world respiratory data for pediatric SMA patients receiving OA who were assessed before and one year after treatment in a multicenter cohort study conducted from 2019 to 2021. Twenty-five OA-treated SMA patients (23 with type 1 and 2 with type 2; median age at treatment 6.1 months, with a range of 0.36–23 months) were included. Sixteen were treatment-naïve, and nine had received various prior treatments. Two patients died due to respiratory failure during the study period. Of the remaining 23 patients, four were put on non-invasive ventilation (NIV), bringing ventilated patients to a total of ten during the post-treatment year. Three patients required permanent NIV support, while 13 did not require any respiratory support. Ventilation time decreased from 14.3 to 11.1 hours per day, and respiratory hospitalizations decreased by 26% (from 0.76 to 0.57 per life year). Fifteen of the 23 patients maintained full oral nutrition at study closure compared to 20 of the 25 at study initiation. This real-world data analysis demonstrates that OA may improve respiratory outcomes in SMA patients. Importantly, compounding factors, such as age at treatment initiation, treatment combinations, and natural history, may influence the respiratory course, thus highlighting the need for standardized long-term management. (Table presented.)
KW - Nusinersen
KW - Onasemnogene abeparvovec
KW - Respiratory
KW - Restrictive lung disease
KW - Spinal muscular atrophy
UR - http://www.scopus.com/inward/record.url?scp=85211123547&partnerID=8YFLogxK
U2 - 10.1007/s00431-024-05886-9
DO - 10.1007/s00431-024-05886-9
M3 - Article
C2 - 39625559
AN - SCOPUS:85211123547
SN - 0340-6199
VL - 184
JO - European Journal of Pediatrics
JF - European Journal of Pediatrics
IS - 1
M1 - 58
ER -