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. 2019 Jun 6;21:138. doi: 10.1186/s13075-019-1917-8

Table 3.

Treatment status

Treatment status Use following csDMARD-IR (first-line biologic agent) Use following first bDMARD-IR (second-line biologic agent)
Abatacept TNFi p value Abatacept TNFi p value
n 92 613 105 212
Stopped treatment, n (%) 47 (51.1) 365 (59.5) 0.1404 60 (57.1) 157 (74.1) 0.0031
 Treatment duration, years, mean (SD) 1.57 (1.68) 2.01 (2.23) 0.1068 1.76 (1.78) 1.33 (1.70) 0.1045
 Reasons for stopping, n (%) 0.1351 0.4409
  Inefficacy 28 (59.6) 171 (46.8) 38 (63.3) 86 (54.8)
  Adverse event 8 (17.0) 76 (20.8) 12 (20.0) 27 (17.2)
  Lost to follow-up 2 (4.3) 21 (5.8) 0 6 (3.8)
  Treatment stopped by the patient 3 (6.4) 14 (3.8) 0 4 (2.5)
  Infections 3 (6.4) 22 (6.0) 2 (3.3) 9 (5.7)
  Death 0 7 (1.9) 3 (5.0) 4 (2.5)
Ongoing treatment 45 (48.9) 248 (40.5) 0.1404 45 (42.9) 55 (25.9) 0.0031
 Treatment duration, years, mean (SD) 4.46 (2.99) 6.25 (3.25) 0.0007 4.57 (2.69) 4.15 (2.68) 0.4364

bDMARD biologic disease-modifying antirheumatic drug, csDMARD conventional synthetic disease-modifying antirheumatic drug, IR inadequate response, TNFi tumor necrosis factor inhibitor