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. 2012 Dec 17;6:429–464. doi: 10.2147/BTT.S36707

Table 5.

American College of Rheumatology (ACR) criteria scores of 20, 50, and 70 network meta-analysis base case results for combination treatments in DMARD-experienced patients: licensed biologic DMARD combinations versus DMARD alone

Fixed effect Random effects


OR v DMARD (95% CrI) % of patients with event (95% CrI) Probability of best, % OR v DMARD (95% CrI) % of patients with event (95% CrI) Probability of best, %
ACR 20
DMARD 29.3% (24.9%, 34%) 0.0% 29.3% (25%, 34%) 0.0%
ABA 10 mg/kg/4 weeks + DMARD 3.288 (2.597, 4.18) 57.6% (49.5%, 65.3%) 0.0% 3.255 (2.056, 5.159) 57.4% (44.8%, 69.2%) 0.0%
ADA 40 mg/2 weeks + DMARD 3.514 (2.65, 4.684) 59.3% (50.5%, 67.6%) 0.0% 3.439 (2.187, 5.303) 58.7% (46.3%, 69.8%) 0.0%
CZP 200 mg/2 weeks + DMARD 10.69 (7.383, 15.69) 81.6% (74.2%, 87.4%) 70.7% 11.06 (6.055, 21.06) 82.1% (70.7%, 90%) 64.2%
ETN 2 × 25 mg/week + DMARD 8.917 (5.25, 15.53) 78.7% (67.5%, 87%) 29.4% 9.341 (4.845, 19.29) 79.5% (66%, 89.2%) 35.1%
GOL 50 mg/4 weeks + DMARD 3.508 (2.18, 5.735) 59.2% (46.2%, 71.3%) 0.0% 3.387 (1.604, 6.863) 58.4% (39.4%, 74.6%) 0.2%
INF 3 mg/kg/8 weeks + DMARD 3.364 (2.71, 4.175) 58.2% (50.5%, 65.4%) 0.0% 3.347 (2.271, 4.983) 58.1% (47.1%, 68.5%) 0.0%
RTX 2 × 1000 mg + DMARD 3.592 (2.378, 5.47) 59.8% (48.3%, 70.5%) 0.0% 3.716 (1.915, 7.418) 60.6% (43.5%, 76.1%) 0.3%
TOC 8 mg/kg/4 weeks + DMARD 4.497 (3.619, 5.61) 65% (57.8%, 71.7%) 0.0% 4.399 (2.704, 7.125) 64.6% (51.7%, 75.5%) 0.2%
ACR 50
DMARD 12% (9.4%, 15.1%) 0.0% 12% (9.4%, 15.1%) 0.0%
ABA 10 mg/kg/4 weeks + DMARD 3.57 (2.718, 4.727) 32.7% (24.9%, 41.9%) 0.0% 3.633 (2.093, 6.341) 33.1% (21.1%, 47.8%) 0.0%
ADA 40 mg/2 weeks + DMARD 3.899 (2.831, 5.446) 34.7% (25.9%, 44.9%) 0.0% 3.87 (2.303, 6.598) 34.5% (22.6%, 49%) 0.1%
CZP 200 mg/2 weeks + DMARD 9.013 (5.636, 14.94) 55.1% (41.7%, 68.5%) 37.2% 9.773 (4.604, 22.65) 57.1% (37.5%, 76.3%) 37.6%
ETN 2 × 25 mg/week + DMARD 10.22 (5.28, 22.3) 58.3% (40.5%, 76%) 61.0% 11.15 (4.947, 27.95) 60.4% (39.2%, 79.8%) 55.6%
GOL 50 mg/4 weeks + DMARD 4.532 (2.521, 8.237) 38.2% (24.5%, 54.3%) 0.8% 4.917 (2.051, 12.34) 40.1% (21.2%, 63.6%) 3.6%
INF 3 mg/kg/8 weeks + DMARD 3.538 (2.724, 4.612) 32.5% (24.9%, 41.2%) 0.0% 3.602 (2.246, 5.924) 32.9% (22.3%, 46.3%) 0.1%
RTX 2 × 1000 mg + DMARD 3.851 (2.28, 6.819) 34.3% (22.5%, 49.6%) 0.2% 4.103 (1.821, 9.73) 35.9% (19.2%, 57.8%) 1.4%
TOC 8 mg/kg/4 weeks + DMARD 5.838 (4.425, 7.773) 44.3% (35%, 54%) 0.8% 5.401 (2.911, 9.561) 42.3% (27.4%, 58%) 1.6%
ACR 70
DMARD 4.7% (3.3%, 6.5%) 0.0% 4.7% (3.4%, 6.5%) 0.0%
ABA 10 mg/kg/4 weeks + DMARD 3.524 (2.435, 5.213) 14.7% (9.4%, 22.6%) 0.0% 3.954 (1.974, 8.8) 16.3% (8.2%, 31.6%) 0.2%
ADA 40 mg/2 weeks + DMARD 3.963 (2.513, 6.5) 16.3% (9.8%, 26.2%) 0.0% 3.868 (1.91, 7.83) 16% (7.9%, 29.2%) 0.1%
CZP 200 mg/2 weeks + DMARD 11.43 (5.472, 27.86) 35.9% (19.8%, 59%) 25.5% 13.18 (4.489, 43.5) 39.2% (17.2%, 69.2%) 28.5%
ETN 2 × 25 mg/week + DMARD 18.99 (5.098, 130.6) 48.3% (19.4%, 86.6%) 69.5% 20.69 (4.921, 158.6) 50.6% (18.8%, 89%) 64.7%
GOL 50 mg/4 weeks + DMARD 4.73 (2.069, 12.2) 18.9% (8.6%, 39%) 1.3% 4.988 (1.401, 18.28) 19.6% (6.2%, 48.4%) 2.7%
INF 3 mg/kg/8 weeks + DMARD 3.549 (2.479, 5.133) 14.8% (9.5%, 22.4%) 0.0% 3.694 (2.021, 7.307) 15.4% (8.3%, 28%) 0.1%
RTX 2 × 1000 mg + DMARD 2.399 (1.168, 5.272) 10.6% (5%, 21.8%) 0.0% 2.644 (0.909, 8.387) 11.5% (4%, 30%) 0.2%
TOC 8 mg/kg/4 weeks + DMARD 7.991 (5.211, 12.79) 28.2% (18.4%, 41.2%) 3.7% 7.656 (3.442, 16.5) 27.2% (13.7%, 46.6%) 3.6%

Notes:

ACR 70 data with continuity correction;

licensed combination had significantly higher odds (based on the 95% CrI) compared to DMARD.

Abbreviations: ABA, abatacept; ADA, adalimumab; ANA, anakinra; CrI, credible interval (Bayesian probability interval); CZP, certolizumab pegol; DMARD, disease-modifying antirheumatic drug (MTX or SUL); ETN, etanercept; exp, experienced; GOL, golimumab; INF, infliximab; MTX, methotrexate; OR, odds ratio; RTX, rituximab; SUL, sulfasalazine; TOC, tocilizumab.