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. 2023 Dec 9;16:17562864231211077. doi: 10.1177/17562864231211077

Table 1.

Demographics and disease characteristics for cladribine-treated patients with RRMS.

Cohort demographics/time points Baseline 6 months* 12 months* 24 months*
Patients per time point, n (%) 23 (100) 16 (69.6) 23 (100) 13 (56.5)
Female patients, n (%) 17 (73.9) 11 (68.7) 17 (73.9) 10 (76.9)
Mean age, years, (± SD) 39.3 (10.7) 40.1 (9.9) 40.3 (10.7) 41.3 (10.9)
EDSS score, median (min, max) 2 (0, 6.5) 2 (0, 5.5) 2 (0, 6) 2 (0, 5.5)
Time since onset of MS, years, mean (± SD) 8.6 (7.4)
Treatment-naïve patients, n (%) 4 (17.4) 4 (25) 4 (17.4) 2 (15.4)
Previous DMT, n (%) 19 (82.6) 12 (75) 19 (82.6) 11 (84.6)
 Platform treatment 8 (34.8) 5 (31.3) 8 (34.8) 3 (23.1)
 Highly active treatment 11 (47.8) 7 (43.8) 11 (47.8) 8 (61.5)

Mean age relates to time point of taking of blood sample. Platform includes the following disease modifying therapies (DMT): teriflunomide, glatiramer acetate, dimethyl fumarate and interferon beta formulation. Highly active includes fingolimod, natalizumab and alemtuzumab.

*

Time after cladribine treatment onset.

DMT, disease modifying therapies; EDSS, expanded disability status scale; max, maximum; min, minimum; MS, multiple sclerosis; n, number; RRMS, relapsing-remitting MS; SD, standard deviation.