Michelson D, Ciafaloni E, Ashwal S, Lewis E, Narayanaswami
P, Oskoui M, Armstrong MJ. Evidence in focus: Nusinersen use in spinal
muscular atrophy: Report of the Guideline Development, Dissemination, and
Implementation Subcommittee of the American Academy of Neurology. Neurology. 2018 Oct 12. [Epub ahead of print]
Abstract
OBJECTIVE:
To identify the level of evidence for use of nusinersen to
treat spinal muscular atrophy (SMA) and review clinical considerations
regarding use.
METHODS:
The author panel systematically reviewed nusinersen clinical
trials for patients with SMA and assigned level of evidence statements based on
the American Academy of Neurology's 2017 therapeutic classification of evidence
scheme. Safety information, regulatory decisions, and clinical context were
also reviewed.
RESULTS:
Four published clinical trials were identified, 3 of which
were rated above Class IV. There is Class III evidence that in infants with
homozygous deletions or mutations of SMN1, nusinersen improves the probability
of permanent ventilation-free survival at 24 months vs a well-defined
historical cohort. There is Class I evidence that in term infants with SMA and
2 copies of SMN2, treatment with nusinersen started in individuals younger than
7 months results in a better motor milestone response and higher rates of
event-free survival than sham control. There is Class I evidence that in
children aged 2-12 years with SMA symptom onset after 6 months of age,
nusinersen results in greater improvement in motor function at 15 months than
sham control. Nusinersen was safe and well-tolerated.
CLINICAL CONTEXT:
Evidence of efficacy is currently highest for treatment of
infantile- and childhood-onset SMA in the early and middle symptomatic phases.
While approved indications for nusinersen use in North America and Europe are
broad, payer coverage for populations outside those in clinical trials remain
variable. Evidence, availability, cost, and patient preferences all influence
decision-making regarding nusinersen use.
No comments:
Post a Comment