Short-Term Safety and Efficacy of Onasemnogene Abeparvovec in 10 Patients with Spinal Muscular Atrophy: Cohort Study
https://doi.org/10.15690/vsp.v20i6S.2367
Abstract
Background. The efficacy and safety of onasemnogene abeparvovec have been demonstrated in patients with spinal muscular atrophy (SMA) in several clinical and observational studies. Gene replacement therapy results in Russian patients with SMA is not investigated yet.
Objective. The aim of the study is to study the safety and efficacy of onasemnogene abeparvovec in children with SMA in real clinical practice.
Methods. The study included patients with proximal 5q SMA administered with onasemnogene abeparvovec. Diagnosis was verified by biallelic deletion in the 7th exon of the SMN1 gene. Gene replacement therapy was administered according to the decision of neurologists consensus in case of the absence of antibodies to the adeno-associated serotype 9 virus. The therapy safety was estimated via clinical and laboratory data from the hospital (at least 7 days) and from outpatient departments (at least 60 days). Efficacy was estimated via CHOP INTEND scale and mastering new motor skills ≥ 6 months after therapy onset.
Results. Treatment outcomes were studied in 10 SMA patients aged 19 months (15; 21). All patients developed at least one clinical manifestation (hyperthermia, vomiting, lethargy and/or loose stool) associated with drug administration during the first week of follow-up. Increased hepatic transaminases activity and monocytosis was recorded in all patients, thrombocytopenia — in 9, neutropenia — in 5, increased troponin I concentration — in 3. In three cases it was necessary to increase the oral prednisolone dose of to 2 mg/kg, in one case — the dexamethasone pulse therapy dose. The therapy efficacy was monitored ≥ 6 months after therapy onset via the CHOP INTEND scale in 2 patients (scores increased by 32 and 19 points, respectively), and via mastering new motor skills in 8 patients (positive dynamics was noted in 7 cases).
Conclusion. The onasemnogene abeparvovec is relatively safe and quite effective for using in real clinical practice
About the Authors
Kristina S. NevmerzhitskayaRussian Federation
Ekaterinburg
Disclosure of interest:
Speaker in Novartis (lecturing for target audience)
Elena Yu. Sapego
Russian Federation
Ekaterinburg
Disclosure of interest:
Speaker in Novartis (lecturing for target audience)
Daria A. Morozova
Russian Federation
Ekaterinburg
Disclosure of interest:
Daria A. Morozova confirmed the absence of a reportable conflict of interests.
References
1. Schorling DC, Pechmann A, Kirschner J. Advances in Treatment of Spinal Muscular Atrophy — New Phenotypes, New Challenges, New Implications for Care. J Neuromuscul Dis. 2020;7(1):1–13. doi: 10.3233/JND-190424
2. Al-Zaidy SA, Mendell JR. From Clinical Trials to Clinical Practice: Practical Considerations for Gene Replacement Therapy in SMA Type 1. Pediatr Neurol. 2019;100:3–11. doi: 10.1016/j.pediatrneurol.2019.06.007
3. Instructions for use of the drug onasemnogene abeparvovec. Available online: https://www.novartis.us/sites/www.novartis.us/files/zolgensma.pdf. Accessed on September 9, 2021.
4. Al-Zaidy SA, Kolb SJ, Lowes L, et al. AVXS-101 (onasemnogene abeparvovec) for SMA1: comparative study with a prospective natural history cohort. J Neuromuscul Dis. 2019;6:307–317. doi: 10.3233/JND-190403
5. Mendell JR, Al-Zaidy SA, Lehman KJ, et al. Five-Year Extension Results of the Phase 1 START Trial of Onasemnogene Abeparvovec in Spinal Muscular Atrophy. JAMA Neurol. 2021;78(7):834–841. doi: 10.1001/jamaneurol.2021.1272
6. Waldrop MA, Karingada C, Storey MA, et al. Gene Therapy for Spinal Muscular Atrophy: Safety and Early Outcomes. Pediatrics. 2020;146(3):e20200729. doi: 10.1542/peds.2020-0729
7. Mathews KD, Iannaccone ST. Combination molecular therapies for spinal muscular atrophy: How much is enough? Muscle & Nerve. 2021;63:279–281. doi: 10.1002/mus.27109
8. Proksimal’naya spinal’naya myshechnaya atrofiya 5q: Clinical guidelines. Ministry of Health of the Russian Federation; 2020. (In Russ). https://cr.minzdrav.gov.ru/recomend/593_1
9. Naveed A, Calderon H. Onasemnogene Abeparvovec (AVXS-101) for the Treatment of Spinal Muscular Atrophy. J Pediatr Pharmacol Ther. 2021;26(5):437–444. doi: 10.5863/1551-6776-26.5.437
10. Kirschner J, Butoianu N, Goemans N, et al. European ad-hoc consensus statement on gene replacement therapy for spinal muscular atrophy. Eur J Paediatr Neurol. 2020;28:38–43. doi: 10.1016/j.ejpn.2020.07.001
11. Vill K, Kölbel H, Schwartz O, et al. One year of newborn screening for SMA — results of a German pilot project. J Neuromuscul Dis. 2019;6(4):503–515. doi: 10.3233/JND-190428
12. De Vivo DC, Bertini E, Swoboda KJ, et al. Nusinersen initiated in infants during the presymptomatic stage of spinal muscular atrophy: interim efficacy and safety results from the Phase 2 NURTURE study. Neuromuscul Disord. 2019;29(11):842–856. doi: 10.1016/j.nmd.2019.09.007
Supplementary files
![]() |
1. Неозаглавлен | |
Subject | ||
Type | Other | |
Download
(68KB)
|
Indexing metadata ▾ |
Review
For citations:
Nevmerzhitskaya K.S., Sapego E.Yu., Morozova D.A. Short-Term Safety and Efficacy of Onasemnogene Abeparvovec in 10 Patients with Spinal Muscular Atrophy: Cohort Study. Current Pediatrics. 2021;20(6s):589-594. https://doi.org/10.15690/vsp.v20i6S.2367