Risk-benefit profile of onasemnogene abeparvovec in older and heavier children with spinal muscular atrophy type 1.
Rebecca FinneganAdnan ManzurPinki MunotAnil DhawanArchana MuruganAnirban MajumdarElizabeth WraigeVasantha GowdaMaria VanegasMarion MainEmer O'ReillyGiovanni BaranelloFrancesco MuntoniMariacristina ScotoPublished in: Neuromuscular disorders : NMD (2024)
Spinal muscular atrophy (SMA) is an autosomal recessive disorder with progressive muscle atrophy and weakness, caused by biallelic mutations in the survival motor neuron 1 (SNM1) gene. Onasemnogene abeparvovec (OA) is an approved gene replacement therapy for patients with SMA. We report on two patients with SMA type 1, weighing 20 kg, previously treated with Nusinersen, who received OA infusion at 7 years of age. To our knowledge, these two patients are the heaviest treated in the real-world and we describe their different courses after gene therapy, including liver impairment requiring long-term steroid treatment and additional immunosuppression, with only transitory improvement in functional outcomes. Our cases illustrate how careful risk-benefit consideration is required in treating older and heavier SMA patients with OA, especially in view of the multiple treatment choices available for older patients with SMA.
Keyphrases
- gene therapy
- newly diagnosed
- physical activity
- end stage renal disease
- community dwelling
- knee osteoarthritis
- intellectual disability
- ejection fraction
- chronic kidney disease
- copy number
- multiple sclerosis
- young adults
- skeletal muscle
- prognostic factors
- peritoneal dialysis
- gene expression
- autism spectrum disorder
- transcription factor
- free survival