Advances in neuromyelitis optica spectrum disorder pathogenesis have allowed the development of targeted drugs. These treatments act on core elements of the disease, including the pro-inflammatory IL-6 pathway (tocilizumab and satralizumab), B cells (rituximab and inebilizumab), and complement (eculizumab). According to recent phase II-III trials, biologics significantly reduced the risk of relapses in aquaporin-4-seropositive patients, whereas results were less striking in the small cohorts of aquaporin-4-seronegative patients. Most adverse events were mild to moderate, with systemic symptoms (headache, arthralgia) or infections (upper respiratory and urinary tracts) being most commonly reported.
Targeting Neuromyelitis Optica Pathogenesis: Results from Randomized Controlled Trials of Biologics / Cacciaguerra, Laura; Tortorella, Paola; Rocca, Maria A; Filippi, Massimo. - In: NEUROTHERAPEUTICS. - ISSN 1933-7213. - 18:(2021), pp. 1623-1636. [10.1007/s13311-021-01055-0]
Targeting Neuromyelitis Optica Pathogenesis: Results from Randomized Controlled Trials of Biologics
Cacciaguerra, Laura;Rocca, Maria A;Filippi, Massimo
2021-01-01
Abstract
Advances in neuromyelitis optica spectrum disorder pathogenesis have allowed the development of targeted drugs. These treatments act on core elements of the disease, including the pro-inflammatory IL-6 pathway (tocilizumab and satralizumab), B cells (rituximab and inebilizumab), and complement (eculizumab). According to recent phase II-III trials, biologics significantly reduced the risk of relapses in aquaporin-4-seropositive patients, whereas results were less striking in the small cohorts of aquaporin-4-seronegative patients. Most adverse events were mild to moderate, with systemic symptoms (headache, arthralgia) or infections (upper respiratory and urinary tracts) being most commonly reported.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.