Active comparator-controlled, rater-blinded study of corticotropin-based immunotherapies for opsoclonus-myoclonus syndrome
- PMID: 22378659
- DOI: 10.1177/0883073811428816
Active comparator-controlled, rater-blinded study of corticotropin-based immunotherapies for opsoclonus-myoclonus syndrome
Erratum in
- J Child Neurol. 2012 Oct;27(10):1364. Dosage error in article text
Abstract
To test the efficacy and safety of corticotropin-based immunotherapies in pediatric opsoclonus-myoclonus syndrome, 74 children received corticotropin alone or with intravenous immunoglobulin (groups 1 and 2, active controls); or both with rituximab (group 3) or cyclophosphamide (group 4); or with rituximab plus chemotherapy (group 5) or steroid sparers (group 6). There was 65% improvement in motor severity score across groups (P < .0001), but treatment combinations were more effective than corticotropin alone (P = .0009). Groups 3, 4, and 5 responded better than group 1; groups 3 and 5 responded better than group 2. The response frequency to corticotropin was higher than to prior corticosteroids (P < .0001). Fifty-five percent had adverse events (corticosteroid excess), more so with multiagents (P = .03); and 10% had serious adverse events. This study demonstrates greater efficacy of corticotropin-based multimodal therapy compared with conventional therapy, greater response to corticotropin than corticosteroid-based therapy, and overall tolerability.
Comment in
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Conventional versus multimodal corticotropin-based immunotherapies for opsoclonus-myoclonus syndrome: where are we?J Child Neurol. 2013 Mar;28(3):416. doi: 10.1177/0883073812469048. J Child Neurol. 2013. PMID: 23400631 No abstract available.
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Response to correspondence on "active comparator-controlled, rater-blinded study of corticotropin-based immunotherapies for opsoclonus-myoclonus syndrome".J Child Neurol. 2013 Mar;28(3):417-8. doi: 10.1177/0883073812469054. J Child Neurol. 2013. PMID: 23400632 No abstract available.
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