Table 3 DMT uptake and usage pattern within RRMS patients.

From: A comparison of multiple sclerosis disease characteristics across three genetically diverse Asian racial groups in Singapore

 

Chinese (n = 82)

Malay (n = 32)

South Asian (n = 63)

Total (n = 177)

p-value

DMT usage (%)

 Yes

60 (73.2)

22 (68.8)

49 (77.8)

131 (74.0)

 

 No

22 (26.8)

10 (31.3)

14 (22.2)

46 (26.0)

0.467

Efficacy of first DMT (%)

 High

23 (38.3)

4 (18.2)

17 (34.7)

44 (33.6)

 

 Low-to-moderate

37 (61.7)

18 (81.8)

32 (65.3)

87 (66.4)

0.248

Type of first DMT (%)

 Interferons

33 (55.5)

17 (77.3)

22 (44.9)

72 (55.0)

 

 Glatiramer acetate

1 (1.7)

2 (4.1)

3 (2.3)

 

 Teriflunomide

1 (1.7)

2 (4.1)

3 (2.3)

 

 Dimethyl fumarate

1 (4.5)

3 (6.1)

4 (3.1)

 

 Leflunomide

1 (1.7)

1 (2.0)

2 (1.5)

 

 Azathioprine

1 (1.7)

1 (4.5)

1 (2.0)

3 (2.3)

 

 Fingolimod

2 (3.3)

4 (8.2)

6 (4.6)

 

 Cladribine

6 (10.0)

5 (10.2)

11 (8.4)

 

 Alemtuzumab

1 (1.7)

3 (13.6)

1 (2.0)

5 (3.8)

 

 Natalizumab

5 (8.3)

1 (2.0)

6 (4.6)

 

 Rituximab

7 (11.7)

5 (10.2)

12 (9.2)

 

 Ocrelizumab

2 (3.3)

1 (2.0)

3 (2.3)

 

 Secukinumab

1 (2.0)

1 (0.8)

0.458

Time taken to initiate DMT from MS diagnosis in days, median (Q1, Q3)

241 (30.5, 975)

152 (28.5, 568)

121 (28, 527)

124 (29, 731)

0.535

Percentage time on DMT, median (Q1, Q3)

 High efficacy

36.4 (6.5, 74.2)

30.7 (0.0, 53.2)

26.5 (0.0, 59.1)

30.0 (0.3, 61.5)

0.225

 Low-to-moderate efficacy

9.9 (0.0, 41.4)

19.9 (9.0, 58.3)

19.6 (0.0, 52.7)

16.6 (0.0, 48.1)

0.188

 All DMTs

69.8 (46.1, 94.1)

58.0 (37.8, 86.5)

68.7 (31.9, 95.3)

65.8 (38.3, 93.1)

0.661

Number of DMT changes, median (Q1, Q3)

1.0 (0.0, 1.0)

1.0 (1.0, 2.0)

1.0 (0.0, 1.5)

1.0 (0.0, 1.0)

0.126

Switched out of initial DMT (%)

 Yes

32 (53.3)

18 (81.8)

27 (55.1)

70 (56.0)

 

 No

28 (46.7)

4 (18.2)

22 (44.9)

55 (44.0)

0.051

  1. Table includes data within RRMS patients only as most PPMS patients were historically not commenced on DMTs.
  2. DMT disease-modifying therapy, PPMS primary progressive multiple sclerosis, RRMS relapsing remitting multiple sclerosis.