Table 1.
Variable | n = 1,364 |
---|---|
Sex | |
Female | 944 (69.3%) |
Male | 418 (30.7%) |
Mean ± SD age on diagnosis of MS, years | 29.6 ± 8.50 |
Mean ± SD time since diagnosis of MS, years | 9.62 ± 5.65 |
Mean ± SD age on starting natalizumab, years | 39.2 ± 8.95 |
Clinical form of MS prior to starting natalizumab | |
Relapsing–remitting | 1,173 (86.8%) |
Secondary progressive | 178 (13.2%) |
Prior MS treatments | |
No | 95 (7.0%) |
Yes | 1,268 (93%) |
One prior treatment | 603 (44.2%) |
Two prior treatments | 431 (31.6%) |
>2 prior treatments | 234 (17.1%) |
Interferon beta 1a SC | 655 (51.7%) |
Interferon beta 1b SC | 447 (35.3%) |
Interferon beta 1a IM | 364 (28.7%) |
Glatiramer acetate | 330 (26.0%) |
Immunosuppressants | 113 (8.9%) |
Mitoxantrone | 98 (7.7%) |
Methotrexate | 7 (0.6%) |
Cyclophosphamide | 9 (0.7%) |
Azathioprine | 4 (0.3%) |
Other treatments | 120 (9.5%) |
EDSS score in year prior to treatment | 3.0 (0.0–8.0) |
Annualized relapse rate in year prior to starting natalizumab | 2.0 (1–14) |
No. of T1 Gd-enhancing lesions prior to natalizumab | |
0 lesions | 530 (47.7%) |
1–5 lesions | 467 (42.0%) |
6–9 lesions | 49 (4.4%) |
>9 lesions | 66 (5.9%) |
EDSS Expanded Disability Status Scale, IM intramuscular, MS multiple sclerosis, SC subcutaneous