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

Table 2.

Characteristics of the patients in the simulated dataset


Other mode of action TNF inhibitor
N 1295 8705
Disease duration (median (IQR) in year) 9.7 (4.5, 17.8) 7.3 (2.9, 14.3)
Treatment duration (median (IQR) in year) 1.2 (0.5, 2.7) 1.6 (0.5, 4.2)
Number of previous bDMARD (number (%))
0 326 (25.2) 4973 (57.1)
1 409 (31.6) 2618 (30.1)
2 294 (22.7) 775 (8.9)
3+ 266 (20.5) 339 (3.9)
Concomitant csDMARD (number (%))
MTX 611 (47.2) 4330 (49.7)
MTX +other 18 (1.4) 248 (2.8)
None 427 (33.0) 3143 (36.1)
Other 239 (18.5) 984 (11.3)
CDAI0 (median (IQR)) 23.2 (16.4, 32.4) 23.0 (14.0, 33.3)
CDAI12 (median (IQR)) 10.2 (5.3, 17.0) 8.0 (3.4, 15.1)
treatment status (number (%))
Ongoing 740 (57.1) 5355 (61.5)
Stopped for adverse event 95 (7.3) 407 (4.7)
Stopped for ineffectiveness 159 (12.3) 755 (8.7)
Stopped for pregnancy 1 (0.1) 11 (0.1)
Stopped for remission 17 (1.3) 41 (0.5)
Stopped for other 57 (4.4) 215 (2.5)
Stopped for unspecified reason 226 (17.5) 1921 (22.1)
LDA 639 (49.3) 5210 (59.9)

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 age, body mass index (BMI), baseline CDAI (CDAI0) and CDAI at 12 months (CDAI12).

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