Skip to main content

Table 4 Reasons for discontinuing, switching, or adding/reducing therapy (2004–2015)

From: Treatment patterns in rheumatoid arthritis patients newly initiated on biologic and conventional synthetic disease-modifying antirheumatic drug therapy and enrolled in a North American clinical registry

 

TNFi monotherapy

Other biologic monotherapya

csDMARD monotherapy

TNFi + csDMARD combination therapy

Other Biologica + csDMARD combination therapy

 

N = 770

  

N = 369

  

N = 2982

  

N = 3022

  

N = 884

  

Factors (number of factors)

Disc. (181)

Swit. (799)

Add (383)

Disc. (97)

Swit. (258)

Add (117)

Disc. (503)

Swit. (2030)

Add (1375)

Disc. (270)

Swit. (2945)

Reduction (1567)

Disc. (68)

Swit.(762)

Reduction (438)

Number of patients with ≥ 1 reason, n

74

265

83

39

100

25

139

654

312

116

954

640

24

1227

165

Total number of reasons

84

390

97

46

129

32

154

821

385

126

1456

694

27

426

192

 Doing well,b n (%)

3 (3.6)

5 (1.3)

1 (1.0)

2 (4.3)

3 (2.3)

0 (0)

14 (9.1)

19 (2.3)

6 (1.6)

10 (7.9)

19 (1.3)

55 (7.9)

2 (7.4)

4 (0.9)

2 (1.0)

 Lack of efficacy,c n (%)

17 (20.2)

184 (47.2)

16 (16.5)

16 (34.8)

69 (53.5)

8 (25.0)

19 (12.3)

232 (28.3)

61 (15.8)

28 (22.2)

615 (42.2)

183 (26.4)

7 (25.9)

207 (48.6)

71 (37.0)

 Other reasons,d n (%)

23 (27.4)

96 (24.6)

61 (62.9)

7 (15.2)

20 (15.5)

15 (46.9)

34 (22.1)

196 (23.9)

236 (61.3)

27 (21.4)

360 (24.7)

186 (26.8)

5 (18.5)

89 (20.9)

42 (21.9)

 Side effects,e n (%)

23 (27.4)

61 (15.6)

9 (9.3)

10 (21.7)

18 (14.0)

3 (9.4)

55 (35.7)

250 (30.5)

28 (7.3)

27 (21.4)

266 (18.3)

142 (20.5)

8 (29.6)

80 (18.8)

40 (20.8)

 Social reasons,f n (%)

18 (21.4)

44 (11.3)

10 (10.3)

11 (23.9)

19 (14.7)

6 (18.8)

32 (20.8)

124 (15.1)

54 (14)

34 (27.0)

196 (13.5)

128 (18.4)

5 (18.5)

46 (10.8)

37 (19.3)

  1. N = number of patients in each cohort; n = number of patients with reasons
  2. anon-TNFi and tsDMARDs
  3. bDoing well includes remissions and similar events
  4. cIncluding inadequate response or failure to maintain initial response
  5. dIncluding therapy no longer needed, formulary restriction, patient preference, physician preference, peer suggestion, fear future side effect, patient doing well, and frequency of administration, temporary interruption, to improve compliance, to improve tolerability, route of administration
  6. eSerious, minor, or fear of side effects
  7. fSocial reasons include cost, preference, and frequency of administration
  8. Add add-on, csDMARD conventional synthetic disease-modifying antirheumatic drug, Disc Discontinue, Swit switch, TNFi tumor necrosis factor inhibitor, tsDMARD targeted synthetic disease-modifying antirheumatic drug