Skip to main content
. 2022 Jan 12;11(1):319–336. doi: 10.1007/s40120-021-00320-w

Table 4.

Clinical and therapeutic characteristics of fingolimod-switching patients

Post-fingolimod treatmenta N (%) F (%) Age, years (mean ± SD)c WA of fingolimod, monthsd EDSS (median score) Annualized relapse rate
Nc Prec Ne Poste Prec WA Postf
Totalb 901 (100.0) 75.4 40.0 ± 10.6 2.0 (1.0, 5.0) 458 3.0 429 3.0 0.37 0.47 0.19
Ocrelizumab 178 (19.8) 71.9 41.8 ± 10.3 3.0 (1.0, 5.0) 136 3.5 101 3.0 0.32 0.41 0.15
Natalizumab 171 (19.0) 80.7 36.6 ± 10.0 2.0 (1.0, 4.0) 79 2.5 74 2.5 0.39 0.66 0.17
Dimethyl fumarate 99 (11.0) 69.7 40.4 ± 9.5 2.0 (1.0, 6.0) 31 2.5 43 3.0 0.21 0.65 0.15
Alemtuzumab 95 (10.5) 75.8 35.5 ± 9.7 3.0 (2.0, 4.5) 33 3.0 45 3.0 0.63 0.53 0.15
Fingolimod after break 85 (9.4) 72.9 40.3 ± 11.0 n.a 39 2.0 40 3.0 0.37 n.a 0.26
Glatiramer acetate 67 (7.4) 79.1 42.9 ± 11.5 1.0 (0.0, 2.0) 24 2.5 29 2.5 0.41 0.16 0.27
Cladribine 46 (5.1) 78.3 39.9 ± 10.4 3.0 (2.0, 5.0) 33 2.5 24 2.25 0.40 0.47 0.09
Daclizumab 35 (3.9) 71.4 40.4 ± 11.7 2.0 (1.0, 2.5) 19 3.0 26 3.0 0.52 0.00 0.34
Interferon beta 33 (3.7) 78.8 39.4 ± 11.7 1.0 (0.0, 7.0) 8 2.25 8 2.5 0.36 0.00 0.44
Teriflunomide 33 (3.7) 87.9 45.3 ± 9.2 3.0 (2.0, 4.0) 15 3.0 15 3.0 0.51 0.27 0.18
Study medication 15 (1.7) 46.7 51.3 ± 9.2 1.0 (0.0, 6.0) 15 4.0 5 5.0 0.00 0.69 0.28
GCS 11 (1.2) 72.7 45.1 ± 9.5 n.a 8 4.75 4 6.25 0.11 0.35 0.00
Rituximab 11 (1.2) 72.7 41.4 ± 10.2 2.0 (2.0, 3.0) 9 3.0 15 3.0 0.44 0.50 0.22

F proportion of female patients, GCS regular glucocorticosteroid pulse therapy, N (%) number of patients (proportion of patients), WA washout period

aGroups with statistically sufficient numbers of patients (N ≥ 10) are shown in detail

bWe excluded 43 of the fingolimod-switching PwMS (N = 944) from this analysis due to missing data on switch dates

cAt last visit/during the last year under fingolimod treatment

dMedian (25% quartile, 75% quartile)

e6–12 months after the initiation of the post-fingolimod treatment

fFrom the start of the post-fingolimod treatment until the end of the observation period