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Table 3 Characteristics of patients who switched or discontinued therapy at time of first switch or discontinuation (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

Characteristic

All switchers

Remission/LDA at time of switch

All discontinuers

Remission/LDA at time of discontinuation

 

N = 3520

N = 1123

N = 2777

N = 1106

Female, n (%)

2798 (79.5)

866 (77.1)

2154 (77.6)

840 (75.9)

BMI, n (%)

 Underweight (BMI < 18.5)

48 (1.4)

11 (1.0)

39 (1.4)

11 (1.0)

 Normal weight (BMI ≥ 18.5 to < 25)

901 (25.6)

322 (28.7)

685 (24.7)

296 (26.8)

 Overweight (BMI ≥ 25 to < 30)

1081 (30.8)

360 (32.1)

889 (32.1)

389 (35.2)

 Obese (BMI ≥ 30)

1484 (42.2)

429 (38.2)

1159 (41.8)

408 (37)

Previous number of csDMARDs, mean (SD)

0.9 (1.0)

0.9 (0.9)

0.8 (1.0)

0.8 (1.0)

Previous TNFi use, n (%)

 1 previous TNFi

1567 (66.5)

545 (76.2)

1079 (63.5)

480 (72.6)

 2+ previous TNFi

790 (33.5)

170 (23.8)

620 (36.5)

181 (27.4)

Previous non-TNFi biologic use, n (%)

 0 previous non-TNFi biologic

2911 (82.7)

978 (87.1)

2243 (80.8)

950 (85.9)

 1 previous non-TNFi biologic

474 (13.5)

118 (10.5)

410 (14.8)

121 (10.9)

 2+ previous non-TNFi biologic

135 (3.8)

27 (2.4)

124 (4.5)

35 (3.2)

Previous biologic/tsDMARD use, n (%)

 1 previous biologic/tsDMARD

1510 (60.5)

537 (70.7)

1003 (55.4)

445 (64.3)

 2 previous biologic/tsDMARD

560 (22.5)

140 (18.4)

453 (25.0)

154 (22.3)

 3+ previous biologic/tsDMARD

424 (17.0)

83 (10.9)

353 (19.5)

93 (13.4)

Current concomitant medication, n (%)

 TNFi onmotherapy

399 (11.3)

121 (10.8)

253 (9.1)

105 (9.5)

 TNFi combination therapy

1308 (37.2)

433 (38.6)

900 (32.4)

378 (34.2)

 MTX monotherapy

363 (10.3)

125 (11.1)

390 (14.0)

135 (12.2)

 MTX + other csDMARD

315 (8.9)

112 (10.0)

328 (11.8)

153 (13.8)

 Other csDMARD

425 (12.1)

162 (14.4)

328 (11.8)

142 (12.8)

Disease activity, mean (SD)

 Tender joint count (28)

6.3 (7.1)

0.7 (1.2)

5.3 (6.8)

0.6 (1.1)

 Swollen joint count (28)

5.1 (5.6)

0.9 (1.4)

4.4 (5.4)

0.8 (1.4)

 Physician Global Assessment (0–100)

30.6 (22.6)

10.8 (10.6)

26.4 (21.8)

10.0 (10.1)

 Patient Global Assessment (0–100)

42.0 (27.5)

20.9 (19.9)

38.9 (27.2)

20.9 (19.9)

 CDAI

18.6 (13.9)

4.7 (3.1)

16.2 (13.3)

4.5 (3.0)

 Patient pain (0–100)

44.7 (28.5)

24.5 (22.6)

41.2 (28.5)

23.5 (22.0)

 DAS28

4.0 (1.6)

2.5 (1.0)

3.8 (1.6)

2.4 (1.0)

 Patient reported fatigue (0–100)

47.4 (29.7)

30.4 (26.6)

44.2 (29.8)

29.1 (26.5)

 hsCRP

11.8 (37.4)

11.4 (49.3)

10.9 (26.6)

9.6 (25.7)

Morning stiffness, n (%)

2836 (82.3)

704 (63.8)

2185 (80.6)

709 (65.5)

Morning stiffness time (hours), mean (SD)

1.6 (3.2)

0.7 (1.9)

1.6 (5.5)

0.7 (2.1)

  1. N = total number of patients in each cohort; n = number of patients with characteristic
  2. BMI body mass index, CDAI, Clinical Disease Activity Index, csDMARD conventional synthetic disease-modifying antirheumatic drug, DAS28 Disease Activity Score-28, hsCRP high-sensitivity C-reactive protein, LDA low disease activity, MTX methotrexate, SD standard deviation, TNFi tumor necrosis factor inhibitor, tsDMARD targeted synthetic disease-modifying antirheumatic drug