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. 2018 Nov 12;2018:9084759. doi: 10.1155/2018/9084759

Table 1.

Baseline characteristics.

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.