Number of patients (samples before/depletion/early repletion/late repletion) |
15 (15/12/10/10) |
Sex, W/M |
8/7 |
EDSS score at start of the study, median, IQR/range |
2.5 ± 3.5 |
Age at start of study, y, mean ± SD |
35.73 ± 8.91 |
Time since MS diagnosis, y, mean ± SD |
10.76 ± 6.31 |
Observation time after initiation of anti-CD20 treatment, y, mean ± SD |
2.68 ± 0.658 |
Last treatment before rituximab (cases) |
|
Dimethylfumarate |
2 |
Fingolimod |
6 |
Glatiramer acetate |
1 |
Natalizumab |
2 |
Azathioprine |
1 |
None (i.e., treatment naive) |
3 |
Washout periods, mo, mean ± SD |
5.42 ± 4.56 |
Prior treatments (cases) |
|
Dimethylfumarate |
2 |
Fingolimod |
9 |
Glatiramer acetate |
4 |
IFNβ-1a |
6 |
IFNβ-1b |
2 |
Natalizumab |
6 |
Azathioprine |
1 |
Cortisone (in last 6 mo before first anti-CD20 treatment) |
4 |
None (i.e., treatment naive) |
3 |
Patients with relapses after therapy initiation |
1, yet with no MRI activity |
Patients with EDSS deterioration after therapy initiation |
1, yet after 19 mo since treatment initiation, without new MRI activity |