Cargando…

Anti-myelin-associated-glycoprotein neuropathy successfully treated with tirabrutinib

BACKGROUND: Anti-myelin-associated-glycoprotein (MAG) neuropathy is a distal, predominantly demyelinating, sensory or sensory-motor polyneuropathy most often developing in the context of an IgM-type monoclonal gammopathy due to monoclonal gammopathy of undetermined significance or lymphoplasmacytic...

Descripción completa

Detalles Bibliográficos
Autores principales: Yasuda, Hajime, Tomizawa, Yuji, Harada, Sakiko, Sasaki, Makoto, Komatsu, Norio, Ando, Jun, Hattori, Nobutaka, Ando, Miki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9557899/
https://www.ncbi.nlm.nih.gov/pubmed/36247137
http://dx.doi.org/10.1016/j.heliyon.2022.e10928
Descripción
Sumario:BACKGROUND: Anti-myelin-associated-glycoprotein (MAG) neuropathy is a distal, predominantly demyelinating, sensory or sensory-motor polyneuropathy most often developing in the context of an IgM-type monoclonal gammopathy due to monoclonal gammopathy of undetermined significance or lymphoplasmacytic lymphoma. Rituximab is considered standard therapy for treatment naïve patients, but optimal treatment methods for relapsed/refractory patients have not been established. CASE PRESENTATION: We demonstrate that tirabrutinib, a second-generation Burton kinase inhibitor, led to drastic improvements of polyneuropathy that were affirmed by nerve conduction studies in a rituximab-refractory anti-MAG neuropathy patient. Tirabrutinib continues to give excellent disease control with no apparent adverse events at 11 months since initiation, and the patient remains free of plasmapheresis sessions which were originally mandatory. CONCLUSION: Tirabrutinib is an extremely promising treatment option for anti-MAG neuropathy.