期刊
NEUROLOGICAL SCIENCES
卷 40, 期 10, 页码 2119-2124出版社
SPRINGER-VERLAG ITALIA SRL
DOI: 10.1007/s10072-019-03959-4
关键词
Multiple sclerosis; Progressive multifocal leukoencephalopathy; Extended doses regimen; Natalizumab; Early diagnosis
Background Progressive multifocal leukoencephalopathy (PML) is a severe adverse event of natalizumab (NTZ). The administration of NTZ with extended interval dosing (EID) has been proposed as a strategy to potentially reduce the incidence of PML while maintaining its therapeutic efficacy. Methods In the current paper, we describe 4 cases of NTZ-PML in EID included in the Italian PML cohort. Results The patients developed PML after at least 38 NTZ infusions. Their John Cunningham virus (JCv) index was > 1.5, and patients had not previously used immunosuppressant. Two patients were asymptomatic at PML onset, while two had mild motor impairment of the right hand and anomia, respectively. All of them had undetectable viral load but one (37 JCv copies/ml). In all patients, MRI revealed unilobar lesions with deferred contrast enhancement suggestive of immune reconstitution. The clinical course ended with a favorable clinical outcome (Delta EDSS up to 1). Conclusions Although PML in EID seems to occur less frequently than in conventional dosing regimen, strict monitoring of high-risk patients contributed to the indolent course observed in the four described cases, characterized by a prolonged pre-symptomatic phase, paucisymptomatic onset, low JCv load, less severe functional impairment during immune reconstitution, and a mild disability burden.
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