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. 2021 Aug 24;41(10):865–874. doi: 10.1007/s40261-021-01073-y

Table 1.

Patient, disease and prior treatment characteristics

Characteristic Value
Females (N = 304), n (%) 192 (63.2)
Age at baseline (N = 304), median (IQR) 38.0 (29.0–45.5)
 ≤ 40 years 184 (60.5)
 > 40 years 120 (39.5)
Disease duration at baseline (N = 299), median (IQR) 6.2 (3.1–10.7)
 ≤ 5 years 123 (41.1)
 > 5 years 176 (58.9)
Relapses in the year prior to natalizumab initiation (N = 304), n (%)
 ≤ 1 140 (46.1)
 > 1 164 (53.9)
ARR in the year prior to natalizumab onset (95% CI), (N = 304) 1.859 (1.708–2.023)
ARR in the 2 years prior to natalizumab onset (95% CI), (N = 304) 1.355 (1.261–1.455)
Baseline EDSS score (N = 286), median (IQR)
 ≤ 3 points 135 (47.2)
 > 3 points 151 (52.8)
Positive anti-JCV serostatus at baseline (N = 72), n (%)a 28 (38.9)
Prior DMTs (N = 304), n (%)
 0 37 (12.2)
 ≥ 1 267 (87.8)
 ≥ 2 128 (42.1)
Prior steroids/immunoglobulins (N = 304), n (%) 148 (48.7)
Prior antineoplastic/immunosuppressive therapy (N = 304), n (%) 20 (6.6)
Natalizumab treatment duration (N = 304), median (IQR), months 58.7 (30.7–78.0)
Patients with permanent natalizumab treatment discontinuation (N = 304), n (%) 154 (50.7)

ARR annualized relapse rate, CI confidence interval, DMT disease-modifying therapy, EDSS Expanded Disability Status Scale, IQR interquartile range; JCV John Cunningham virus, N number of patients with available data

aAnti-JCV testing at baseline was not a prerequisite during the enrollment period of the study