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. 2022 Jan 13;81(5):729–736. doi: 10.1136/annrheumdis-2021-221477

Table 1.

Characteristics of the patients under treatment in the initial real-world register collection


Other mode of actions TNF inhibitor
N 6067 40 767
Disease duration (median (IQR) in year) 9.8 (4.6, 17.9) 7.4 (2.9, 14.6)
Treatment duration (median (IQR) in year) 1.2 (0.5, 2.7) 1.7 (0.6, 4.3)
Number of previous bDMARD (number (%))
0 1451 (23.9) 23 016 (56.5)
1 2019 (33.3) 12 269 (30.1)
2 1383 (22.8) 3896 (9.6)
3+ 1214 (20.0) 1586 (3.9)
Concomitant csDMARD (number (%))
MTX 2982 (49.2) 20 062 (49.2)
MTX +other 68 (1.1) 1080 (2.6)
None 1907 (31.4) 15 047 (36.9)
Other 1110 (18.3) 4578 (11.2)
CDAI0 (median (IQR)) 23.4 (16.5, 32.0) 23.0 (13.9, 33.5)
CDAI12 (median (IQR)) 10.0 (5.0, 17.3) 7.0 (2.9, 14.0)
Treatment status (number (%))
Ongoing 3336 (55.0) 24 968 (61.2)
Stopped for adverse event 459 (7.6) 1876 (4.6)
Stopped for ineffectiveness 748 (12.3) 3369 (8.3)
Stopped for pregnancy 5 (0.1) 53 (0.1)
Stopped for remission 62 (1.0) 189 (0.5)
Stopped for other 313 (5.2) 1089 (2.7)
Stopped for unspecified reason 1144 (18.9) 9223 (22.6)
Missing CDAI12 (number (%)) 1680 (27.7) 9415 (23.1)
Number (%) of patients stopping after 1 year (number (%)) 1017 (16.8) 6081 (14.9)
LDA at 12 month (number (%)) 1811 (51.4) 15 873 (63.7)

Number of observations (N), number and proportion of patients having 0, 1, 2, 3 and more (3+) previous biological DMARD, of patient having methotrexate alone (MTX), methotrexate with other csDMARD (MTX +other), at least an csDMARD other than MTX (other) or no concomitant synthetic DMARD treatment (none), median (IQR) value of baseline CDAI (CDAI0) and CDAI at 12 months (CDAI12).

CDAI, Clinical Disease Activity Index; csDMARD, conventional synthetic disease-modifying antirheumatic drugs; TNF, tumour necrosis factor.