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. 2018 Mar 21;9:138. doi: 10.3389/fphar.2018.00138

Table 1.

Patient characteristics in the studies included in the analysis.

Study, first author, year Blinding Follow up (weeks) Sizes Outcomes Intervention Cases Female Disease durations (year) Age (year)
Swefot (TBD), van Vollenhoven et al., 2009 Open-label 52 258 ①③④ cDMARDs 130 101 0.525 (0.3) 53.9 (13.9)
IFX+MTX 128 97 0.517 (0.29) 51.1 (13.3)
Nishimoto, 2004, Nishimoto et al., 2004 Double-blind 12 162 ①③ PBO 53 39 8.4 53
TCZ 54 40 7.3 53.5
TCZ 55 46 8.3 56
GUEPARD, Soubrier et al., 2009 Unblinded 52 65 ①② cDMARDs 32 26 4.4 49.3 (15.2)
ADA+MTX 33 26 4.4 46.3 (16.3)
ASPIRE, St Clair et al., 2004 Not specified 46 1,004 ①②③④ cDMARDs 282 212 0.9 (0.7) 50 (13)
IFX+MTX 359 255 0.8 (0.7) 51 (12)
IFX+MTX 363 247 0.9 (0.8) 50 (130)
OPTIMA, Kavanaugh et al., 2013 Double-blind 26 1,032 ①②③④ ADA+MTX 515 380 0.33 (0.3) 50.7 (14.5)
cDMARDs 517 382 0.375 (0.6) 50.4 (13.6)
BeST, Goekoop-Ruiterman et al., 2008 Double-blind 26 254 ①③④ cDMARDs 126 86 0.44 54 (13)
IFX+MTX 128 85 0.62 54 (14)
GO-BEFORE, Emery et al., 2009 Double-blind 24 637 ①②③④ cDMARDs 160 134 2.9 (4.80) 48.6 (12.91)
GOL 159 134 4.1 (5.60) 48.2 (12.85)
GOL+MTX 159 135 3.5 (5.65) 50.9 (11.32)
GOL+MTX 159 125 3.6 (6.09) 50.2 (11.87)
COMET, Emery et al., 2008a Double-blind 104 528 ①②③④ cDMARDs 263 191 0.78 (0.03) 52.3 (0.8)
ETN+MTX 265 196 0.73 (0.03) 50.5 (0.9)
Durez2007, Durez et al., 2007 Double-blind 52 29 cDMARDs 14 10 0.45 (0.29) 53.8 (15.2)
IFX+MTX 15 5 0.36 (0.31) 50.0 (9.9)
PREMIER, Breedveld et al., 2006 Double-blind 104 799 ①② ADA+MTX 268 193 0.7 (0.8) 51.9 (14.0)
ADA 274 212 0.7 (0.8) 52.1 (13.5)
cDMARDs 257 190 0.8 (0.9) 52.0 (13.1)
Bathon, 2000, Bathon et al., 2000 Double-blind 52 632 ①③ cDMARDs 217 163 1 (0.92) 49 (13)
ETN 208 156 0.92 (0.83) 50 (13)
ETN 207 153 1 (0.92) 51 (13)
Bejarano, 2008, Bejarano et al., 2008 Double-blind 56 128 ①②③④ cDMARDs 73 39 0.66 (0.45) 47 (9)
ADA+MTX 75 44 0.79 (0.5) 47 (9)
HITHARD, Detert et al., 2013 Double-blind 48 172 ①②④ ADA+MTX 87 61 0.15 (0.17) 47.2 (12.12)
cDMARDs 85 57 0.13 (0.14) 52.5 (14.34)
Quinn, 2005, Quinn et al., 2005 Double-blind 52 20 ①② IFX+MTX 10 N/A 0.62 (0.38) 51.3 (9.5)
cDMARDs 10 N/A 0.5 (0.31) 53.1 (13.7)
OPERA, Hørslev-Petersen et al., 2014 Double-blind 52 180 ①④ ADA+MTX 89 56 88 days 56.2
cDMARDs 91 63 83 days 54.2
C-EARLY, Emery et al., 2016 Double-blind 52 868 ①②③④ cDMARDs 213 170 0.24 (0.24) 51.2 (13.0)
CZP+MTX 655 497 0.24 (0.38) 50.4 (13.6)
U-Act-Early, Bijlsma et al., 2016 Double-blind 24 317 ①③④ TCZ+MTX 106 65 24.5 days 53
TCZ 103 78 25.5 days 55
cDMARDs 108 69 27.0 days 53.5
Function, Burmester et al., 2013 Double-blind 52 1,157 ①②③④ cDMARDs 287 229 0.4 (0.48) 49.6 (13.1)
TCZ+MTX 288 228 0.4 (0.49) 51.2 (13.84)
TCZ+MTX 290 228 0.5 (0.53) 49.5 (13.70)
TCZ 292 219 0.5 (0.48) 49.9 (13.22)
C-OPERA, Atsumi et al., 2015 Double-blind 24 316 ②③④ cDMARDs 157 127 N/A 49 (10.3)
CZP+MTX 159 129 N/A 49.4 (10.6)
RADIATE, Emery et al., 2008b Double-blind 24 489 ①②③④ TCZ+MTX 170 84 12.6 (9.3) 53.9 (12.7)
TCZ+MTX 161 81 11.0 (8.5) 50.9 (12.5)
cDMARDs 158 79 11.4 (9.2) 53.4 (13.3)

① ACR.

② Remission.

③ adverse effects (AEs).

④ serious adverse effects.

cDMARDs: conventional disease-modifying antirheumatic drugs; MTX: methotrexate; ADA: adalimumab; CZP: certolizumab; ETN: etanercept; GOL: golimumab; IFX: infliximab; TCZ: PBO: tocilizumab; placebo.