A multicenter, non-interventional study to evaluate the disease activity in Multiple Sclerosis after withdrawal of Natalizumab in Portugal

被引:4
作者
Ladeira, Filipa [1 ]
Braz, Luis [2 ]
Salgado, Paula [3 ]
Vaz, Soraia [4 ]
Leitao, Lia [5 ]
Felix, Catarina [6 ]
Correia, Ana Sofia [1 ,7 ]
da Silva, Ana Martins [3 ]
Salgado, Vasco [5 ]
Ferreira, Fatima [6 ]
Vale, Jose [8 ]
de Sa, Maria Jose [2 ,9 ]
Capela, Carlos [4 ]
机构
[1] Ctr Hosp Lisboa Ocidental, Hosp Egas Moniz, Neurol Dept, R Junqueira 126, P-1349019 Lisbon, Portugal
[2] Ctr Hosp Sao Joao, Neurol Dept, Alameda Prof Hernani Monteiro, P-4200319 Oporto, Portugal
[3] CHU Porto, Hosp Santo Antonio, Neurol Dept, Largo Prof Abel Salazar, P-4099001 Oporto, Portugal
[4] Ctr Hosp Lisboa Cent, Hosp Santo Antonio Capuchos, Neurol Dept, Alameda Santo Antonio Capuchos, P-1169050 Lisbon, Portugal
[5] Hosp Prof Doutor, Neurol Dept, IC19, P-2720276 Amadora, Portugal
[6] Ctr Hosp & Univ Algarve, Hosp Faro, Dept Neurol, Rua Leao Penedo, P-8000386 Faro, Portugal
[7] Univ Nova Lisboa, Fac Ciencias Med, Nova Med Sch, CEDOC, Campo Martires Patria 130, P-1169056 Lisbon, Portugal
[8] Hosp Beatriz Angelo, Neurol Dept, Ave Carlos Teixeira 514, Loures, Portugal
[9] Univ Fernando Pessoa, Fac Hlth Sci, Praca 9 Abril 349, P-4249004 Oporto, Portugal
关键词
Natalizumab discontinuation; Reactivation; Rebound; Relapsing-remitting Multiple sclerosis; ACTIVITY RETURN; MS; CESSATION; DISCONTINUATION; INTERRUPTION; FINGOLIMOD; THERAPY;
D O I
10.1016/j.clineuro.2019.105390
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objectives: Natalizumab (NTZ) is very effective for treatment of relapsing-remitting multiple sclerosis (RAMS), its use is mainly limited by safety issues. Discontinuation of NTZ is associated with recurrence of disease activity (reactivation and rebound). The best strategy for subsequent therapy and the predictive factors for recurrence in such patients are areas of active research. We aimed to evaluate predictors of reactivation in a multicentric study. Patients and methods: Multicentric retrospective observational study in five Portuguese MS referral centers. Demographic, clinical and imagiological data were collected in the year prior, during and in the year following NTZ discontinuation. Predictors of reactivation and rebound after NTZ suspension were studied using a multivariate Cox model. Results: Sixty-nine patients were included. They were mainly non-naive patients (97%), with a mean age of 29.1 +/- 8.3 years at diagnosis, and a mean age of 37.2 +/- 10.3 years at NTZ initiation. The mean annualized relapse rate (ARR) previous, during and after NTZ was 1.6 +/- 1.2, 0.2 +/- 0.5 and 0.6 +/- 1.0, respectively. The median EDSS before, during and after NTZ was 3.5 (IQR 3.3), 3.5 (IQR 3.5) and 4.0 (IQR 3.8), respectively. The median number of infusions was 26.0 (IQR 12.5) and the main reason to NTZ discontinuation was progressive multifocal leukoencephalopathy (PML) risk (70%). After NTZ suspension, reactivation was observed in 25 (36%) patients after a median time of 20.0 (IQR 29.0) weeks. Reactivation predictors in our sample included NTZ suspension for reasons other than PML (adjusted HR = 0.228, 95% CI [0.084- 0.616], p = 0.004), ARR before NTZ (adjusted HR = 1.914 95% [CI 1.330-2.754], p < 0.001) and a longer disease duration at time of NTZ initiation (adjusted HR = 1.154, 95% CI [1.020-1.306], p = 0.023). Rebound occurred in 5 (7%) patients after a median time of 20 (IQR 34.5) weeks. Conclusion: Significant predictors of disease reactivation in our cohort were discontinuation of NTZ for reasons other than PML risk, higher disease activity before NTZ treatment, and longer disease duration. Our study provides valuable data of portuguese patients after NTZ withdrawal.
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