Patient and Caregiver Outcomes After Onasemnogene Abeparvovec Treatment: Findings from the Cure SMA 2021 Membership Survey

Introduction Onasemnogene abeparvovec (OA) is the only gene replacement therapy currently approved for spinal muscular atrophy (SMA) treatment. We sought to assess real-world patient and caregiver outcomes after OA treatment for SMA. Methods Patients who received OA were identified from the 2021 Cur...

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Veröffentlicht in:Advances in therapy 2023-12, Vol.40 (12), p.5315-5337
Hauptverfasser: Toro, Walter, Yang, Min, Georgieva, Mihaela, Anderson, Annika, LaMarca, Nicole, Patel, Anish, Akbarnejad, Hanane, Dabbous, Omar
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Sprache:eng
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Zusammenfassung:Introduction Onasemnogene abeparvovec (OA) is the only gene replacement therapy currently approved for spinal muscular atrophy (SMA) treatment. We sought to assess real-world patient and caregiver outcomes after OA treatment for SMA. Methods Patients who received OA were identified from the 2021 Cure SMA Membership Survey. Those treated at 6–23 months of age were matched to non–patients treated with OA on the basis of age at the time of survey and survival motor neuron 2 gene copy number. Patient characteristics, motor milestones, and resource and supportive care use, as well as caregiver proxy-reported health-related quality of life (HRQOL), were described. Caregiver unmet needs and HRQOL were also assessed. Results Of the 614 patients in the survey, 64 received OA, and 17 were matched with 28 non–OA-treated patients. In general, a greater percentage of OA-treated patients achieved various motor milestones, including 100% sitting without support and 58.8% walking with assistance. OA-treated patients also had numerically lower rates of hospitalization and surgery. None required tracheostomy with a ventilator. The rate of using oxygen or a breathing machine for more than 16 h was also lower for OA-treated patients. OA-treated patients had less frequent trouble swallowing. HRQOL was reported to be similar to non–OA-treated patients. Caregivers of OA-treated patients reported better patient mobility scores and less work impairment. Conclusions The study suggests that treatment with OA is associated with greater rates of motor milestone achievements and less resource and supportive care use for patients with SMA treated at 6–23 months of age in the real world. For caregivers, it may also potentially reduce unmet needs, improve HRQOL, and reduce work impairment.
ISSN:0741-238X
1865-8652
DOI:10.1007/s12325-023-02685-w