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. 2019 Dec 20;59(9):2325–2333. doi: 10.1093/rheumatology/kez602

Table 1.

Baseline characteristics at start of U-Act-Early of patients included in the post-trial follow-up study (n = 226)a

TCZ+MTX (n = 75) TCZ (n = 79) MTX (n = 72) P-value
Female, n (%) 47 (63) 61 (77) 48 (67) 0.13
RF+, n (%) 53 (71) 55 (71) 58 (82) 0.21
Anti CCP+, n (%) 51 (68) 54 (69) 56 (79) 0.28
RF+ and/or anti-CCP+, n (%) 55 (73) 62 (79) 64 (89) 0.06
Caucasian, n (%) 71 (95) 77 (97) 71 (99) 0.47
Smoking status, n (%) 0.81
 Never smoked 29 (39) 34 (43) 28 (39)
 Quit smoking 21 (28) 24 (30) 25 (35)
 Current smoker 25 (33) 21 (27) 19 (26)
Age, mean (s.d.), years 53.8 (11.2) 55.5 (11.6) 53.7 (12.9) 0.63
Symptom duration, median (IQR), days 27 (18–43) 25 (19–43) 28 (16–46) 0.96
DAS28, mean (s.d.) 5.1 (1.1) 5.3 (1.1) 5.0 (1.2) 0.33
HAQ, median (IQR) 1.3 (0.6–1.6) 1.3 (0.9–1.8) 1.0 (0.5–1.4) 0.17
SvdH score, median (IQR) 0 (0–0) 0 (0–2) 0 (0–1) 0.24
a

According to their initial treatment strategy as randomized. Anti-CCP: anti-cyclic citrullinated peptide antibodies; DAS28: disease activity score assessing 28 joints; HAQ: health assessment questionnaire; IQR: interquartile range; MTX: methotrexate + placebo–tocilizumab initiation strategy group; RF: rheumatoid factor; SvdH: Sharp–van der Heijde score; TCZ: tocilizumab + placebo–methotrexate initiation strategy group; TCZ+MTX: tocilizumab + methotrexate initiation strategy group.