Table 1.
Fingolimod (N = 271) |
Dimethyl fumarate (N = 342) |
||||
---|---|---|---|---|---|
N or mean | % or SD | N or mean | % or SD | p value | |
Disease duration (years, SD) | 11.5 | 7.5 | 11.1 | 7.4 | 0.259 |
Age (years, SD) | 42.5 | 11.4 | 45.8 | 12.2 | <0.001 |
<18 years old | 5 | 1.8% | 5 | 1.5% | 0.710 |
>55 years old | 39 | 14.4% | 81 | 23.7% | 0.004 |
Gender, female | 195 | 72.0% | 238 | 69.6% | 0.523 |
Race | 0.186 | ||||
White | 233 | 86.3% | 281 | 82.2% | |
Black, African American | 4 | 1.5% | 15 | 4.4% | |
Other | 11 | 4.1% | 13 | 3.8% | |
Not available | 23 | 8.1% | 33 | 9.6% | |
Ethnicity | 0.589 | ||||
Hispanic | 15 | 5.5% | 15 | 4.4% | |
Non-Hispanic | 226 | 83.4% | 284 | 83.0% | |
Not available | 30 | 11.1% | 43 | 12.6% | |
Type of multiple sclerosis | <0.001 | ||||
Relapsing–remitting | 244 | 90.0% | 265 | 77.5% | |
Secondary progressive | 23 | 8.5% | 54 | 15.8% | |
Primary progressive | 4 | 1.5% | 23 | 6.7% | |
Previous DMTa | <0.001 | ||||
Interferons | 36 | 13.3% | 49 | 14.3% | |
Glatiramer acetate | 49 | 18.1% | 106 | 31.0% | |
Natalizumab | 115 | 42.4% | 65 | 19.0% | |
Rituximab | 1 | 0.4% | 9 | 2.6% | |
Fingolimod | N/A | N/A | 24 | 7.0% | |
Dimethyl fumarate | 1 | 0.4% | N/A | N/A | |
None | 66 | 24.4% | 84 | 24.6% | |
Other | 3 | 1.1% | 5 | 1.5% | |
Mean time between Previous DMT and study drug (SD) | 1.05 (N = 205) | 1.22 | 0.75 (N = 258) | 1.29 | <0.001 |
Baseline MRI available for review | 0.004 | ||||
Available | 235 | 86.7% | 320 | 93.6% | |
Unavailable | 36 | 13.3% | 22 | 6.4% | |
Contrast enhancement on baseline MRI | 57 (N = 232) | 24.6% | 44 (N = 302) | 14.6% | 0.003 |
Disease burden on baseline MRI | 0.001 | ||||
Mild | 100 | 36.9% | 170 | 49.7% | |
Moderate | 76 | 28.0% | 94 | 27.5% | |
Severe | 45 | 16.6% | 29 | 8.5% | |
Missing | 50 | 18.5% | 49 | 14.3% |
Within six months prior to starting study drug.
DMT: disease-modifying therapy; MRI: magnetic resonance imaging.