Emilie Sala1, Florence Robert-Varvat1, Stéphane Paul2, Jean-Philippe Camdessanché1, Jean-Christophe Antoine3. 1. Department of Neurology, University Hospital of Saint-Etienne, France; Reference Center for Rare Neuromuscular Diseases, University Hospital of Saint-Etienne, France. 2. Laboratory of Immunology, University Hospital of Saint-Etienne, France. 3. Department of Neurology, University Hospital of Saint-Etienne, France; Reference Center for Rare Neuromuscular Diseases, University Hospital of Saint-Etienne, France. Electronic address: j.christophe.antoine@chu-st-etienne.fr.
Abstract
BACKGROUND: Patients with peripheral neuropathy and anti-MAG monoclonal IgM may respond to Rituximab, a humanized monoclonal anti-CD20 antibody. METHODS: We report on three patients with peripheral neuropathy and anti-MAG monoclonal IgM who deteriorated under Rituximab and reviewed seven previously published cases. RESULTS: Worsening was acute and severe, and occurred during the treatment period. All the patients improved after deterioration but at final evaluation only one was improved comparatively to baseline, five were worsened and four were stabilized. Deterioration was not clearly associated with an increase of the anti-MAG antibody titer. Two patients received Rituximab prior or after the course which induced worsening without adverse reaction. CONCLUSION: Although rare, acute worsening of the neuropathy can occur after Rituximab. The deterioration is however reversible within some weeks to several months.
BACKGROUND:Patients with peripheral neuropathy and anti-MAG monoclonal IgM may respond to Rituximab, a humanized monoclonal anti-CD20 antibody. METHODS: We report on three patients with peripheral neuropathy and anti-MAG monoclonal IgM who deteriorated under Rituximab and reviewed seven previously published cases. RESULTS: Worsening was acute and severe, and occurred during the treatment period. All the patients improved after deterioration but at final evaluation only one was improved comparatively to baseline, five were worsened and four were stabilized. Deterioration was not clearly associated with an increase of the anti-MAG antibody titer. Two patients received Rituximab prior or after the course which induced worsening without adverse reaction. CONCLUSION: Although rare, acute worsening of the neuropathy can occur after Rituximab. The deterioration is however reversible within some weeks to several months.
Authors: M Baron; P Lozeron; S Harel; D Bengoufa; M Vignon; B Asli; M Malphettes; N Parquet; A Brignier; J P Fermand; N Kubis; Bertrand Arnulf Journal: J Neurol Date: 2017-05-08 Impact factor: 4.849