'Minimal symptom expression' in patients with acetylcholine receptor antibody-positive refractory generalized myasthenia gravis treated with eculizumab.
dc.contributor.author | Vissing, John | |
dc.contributor.author | Jacob, Saiju | |
dc.contributor.author | Fujita, Kenji P | |
dc.contributor.author | O'Brien, Fanny | |
dc.contributor.author | Howard, James F | |
dc.contributor.author | REGAIN study group | |
dc.date.accessioned | 2023-07-19T20:20:01Z | |
dc.date.available | 2023-07-19T20:20:01Z | |
dc.date.issued | 2020-07 | |
dc.date.updated | 2023-07-19T20:20:00Z | |
dc.description.abstract | BackgroundThe efficacy and tolerability of eculizumab were assessed in REGAIN, a 26-week, phase 3, randomized, double-blind, placebo-controlled study in anti-acetylcholine receptor antibody-positive (AChR+) refractory generalized myasthenia gravis (gMG), and its open-label extension.MethodsAttainment of 'minimal symptom expression' was evaluated using patient-reported outcome measures of gMG symptoms [MG activities of daily living scale (MG-ADL), 15-item MG quality of life questionnaire (MG-QOL15)] at the completion of REGAIN and during the open-label extension. 'Minimal symptom expression' was defined as MG-ADL total score of 0-1 or MG-QOL15 total score of 0-3.ResultsAt REGAIN week 26, more eculizumab-treated patients achieved 'minimal symptom expression' versus placebo [MG-ADL: 21.4% vs 1.7%; difference 19.8%; 95% confidence interval (CI) 8.5, 31.0; p = 0.0007; MG-QOL15: 16.1% vs 1.7%; difference 14.4%; 95% CI 4.3, 24.6; p = 0.0069]. During the open-label extension, the proportion of patients in the placebo/eculizumab group who achieved 'minimal symptom expression' increased after initiating eculizumab treatment and was sustained through 130 weeks of open-label eculizumab (MG-ADL: 1.7 to 27.8%; MG-QOL15: 1.7 to 19.4%). At extension study week 130, similar proportions of patients in the eculizumab/eculizumab and placebo/eculizumab groups achieved 'minimal symptom expression' (MG-ADL: 22.9% and 27.8%, respectively, p = 0.7861; MG-QOL15: 14.3% and 19.4%, respectively, p = 0.7531). The long-term tolerability of eculizumab was consistent with previous reports.ConclusionsPatients with AChR+ refractory gMG who receive eculizumab can achieve sustained 'minimal symptom expression' based on patient-reported outcomes. 'Minimal symptom expression' may be a useful tool in measuring therapy effectiveness in gMG.Trial registrationClinicalTrials.gov NCT01997229, NCT02301624. | |
dc.identifier | 10.1007/s00415-020-09770-y | |
dc.identifier.issn | 0340-5354 | |
dc.identifier.issn | 1432-1459 | |
dc.identifier.uri | ||
dc.language | eng | |
dc.publisher | Springer Science and Business Media LLC | |
dc.relation.ispartof | Journal of neurology | |
dc.relation.isversionof | 10.1007/s00415-020-09770-y | |
dc.subject | REGAIN study group | |
dc.subject | Humans | |
dc.subject | Myasthenia Gravis | |
dc.subject | Receptors, Cholinergic | |
dc.subject | Immunologic Factors | |
dc.subject | Autoantibodies | |
dc.subject | Activities of Daily Living | |
dc.subject | Double-Blind Method | |
dc.subject | Quality of Life | |
dc.subject | Adult | |
dc.subject | Aged | |
dc.subject | Middle Aged | |
dc.subject | Female | |
dc.subject | Male | |
dc.subject | Antibodies, Monoclonal, Humanized | |
dc.subject | Patient Reported Outcome Measures | |
dc.title | 'Minimal symptom expression' in patients with acetylcholine receptor antibody-positive refractory generalized myasthenia gravis treated with eculizumab. | |
dc.type | Journal article | |
pubs.begin-page | 1991 | |
pubs.end-page | 2001 | |
pubs.issue | 7 | |
pubs.organisational-group | Duke | |
pubs.organisational-group | School of Medicine | |
pubs.organisational-group | Clinical Science Departments | |
pubs.organisational-group | Neurology | |
pubs.organisational-group | Neurology, Neuromuscular Disease | |
pubs.publication-status | Published | |
pubs.volume | 267 |
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