Table 1.
Baseline characteristics (n = 89) | |
---|---|
Age (mean, SD) | 40.5 ± 12.3 years |
Sex (n, %) | n = 31 (34.8%); male |
n = 58 (65.2%); female | |
Disease duration (mean, SD) | 7.9 ± 6.2 years |
Type of MS (n, %) | n = 59 (66.3%); RRMS |
n = 30 (33.7%); progressive MS | |
Time since onset of PMS (mean, SD) | 3.0 ± 2.1 years |
Baseline EDSS score (mean, SD, range) | 2.25 ± 1.2 (0–6.5) |
Number of relapses in previous two years (mean, SD, range) | 1.6 ± 1.6 (0–8) |
Time between last relapse and RTX initiation (median, range) | 3 months (0–20) |
Median number of RTX infusions (range) | 4 infusions (2–22) |
Proportion of patients with 2000 mg initial loading dose (n) | 76.4% (n = 68) |
Baseline MRI findings (%, n) | 28% (n = 24); stable |
36% (n = 31); new T2 nonenhancing lesions | |
36% (n = 31); enhancing lesions | |
| |
Proportion of patients with prior DMT use (%, n) | 11.2% (n = 10); treatment naïve |
34.8% (n = 31); one previous DMT | |
30.3% (n = 27); 2 previous DMTs | |
11.2% (n = 10); 3 previous DMTs | |
9.0% (n = 8); 4 previous DMTs | |
1.2% (n = 1); 5 previous DMTs | |
2.3% (n = 2); 6 previous DMTs | |
| |
Last DMT prior to RTX | 55.7% (n = 44); IFN |
17.7% (n = 14); fingolimod | |
11.4% (n = 9); natalizumab | |
5.1% (n = 4); mitoxantrone | |
10.1% (n = 8); others (AZA, mycophenolate, methotrexate, teriflunomide, cyclophosphamide) | |
| |
Reasons for switching to RTX | 87.3% (n = 69); inefficacy |
5.1% (n = 4); positive JCV | |
2.5% (n = 2); adverse events | |
2.5% (n = 2); nonavailability of other DMTs | |
2.5% (n = 2); personal decision | |
RTX treatment duration (mean, SD) | 22.2 ± 24.8 months |
SD = standard deviation; MS = multiple sclerosis; RRMS = relapsing-remitting multiple sclerosis; PMS = progressive multiple sclerosis; EDSS = expanded disability status scale; RTX = rituximab; MRI = magnetic resonance imaging; DMT = disease-modifying therapy; IFN = interferon; AZA = azathioprine; JCV = John Cunningham virus.