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. 2013 Mar 5;52(6):986–997. doi: 10.1093/rheumatology/ket018

Table 1.

Baseline demographics and clinical characteristics

ACQUIRE [11] ALLOWa [17] ACCOMPANY [15] ATTUNE [16] AMPLE [19]
Published inclusion criteria ≥10 swollen joints, ≥12 tender joints, CRP ≥0.8 mg/dl DAS28 (CRP) ≥3.2 and ≤5.1 Global Assessment of Disease Activity VAS >20 ≥4 years of treatment with i.v. abatacept in AIM or ATTAIN trial ≤5 years disease duration, DAS28 (CRP) ≥3.2, history of anti-CCP or RF seropositivity, or elevated ESR or CRP
Patient population Active RA, MTX-IR Active RA, MTX-IR Active RA, IR to ≥1 DMARD (MTX-naïve or MTX-IR) Active RA, MTX-IRb Active RA, anti-TNF IRc Active RA, MTX-IR, biologic-naïve
Treatment s.c. abatacept + MTX i.v. abatacept + MTX s.c. abatacept + MTX s.c. abatacept with/without MTX s.c. abatacept s.c. abatacept + MTX s.c. adalimumab + MTX
Continuous Withdrawal/ reintroduction
n 736 721 40 80 100 71 52 318 328
Age, years 49.9 (13.2) 50.1 (12.6) 48.9 (14.2) 49.1 (12.8) 54.0 (10.9) 52.8 (13.8) 56.5 (10.2) 51.4 (12.6) 51.0 (12.8)
Weight, kg 72.0 (18.0) 71.8 (17.6) 67.9 (15.8) 68.9 (14.7) 83.1 (20.6) NR NR 80.8 (20.3) 80.1 (20.7)
Gender, % female 84.4 80.4 85.0 83.8 75.0 83.1 80.8 81.4 82.3
Ethnicity, % Caucasian 74.7 74.5 95.0 93.8 76.0 98.6 90.4 80.8 78.0
Disease duration, years 7.6 (8.1) 7.7 (7.8) 7.4 (7.7) 6.2 (5.8) 10.1 (11.1) NR NR 1.9 (1.4) 1.7 (1.4)
DAS28 (CRP) 6.2 (0.9) 6.2 (0.8) 4.8 (0.8) 4.8 (0.8) 5.4 (1.4) 3.3 (1.3) 3.6 (1.2) 5.5 (1.1) 5.5 (1.1)
HAQ-DI score 1.7 (0.7) 1.7 (0.7) 1.4 (0.7) 1.3 (0.7) 1.4 (0.7) 0.9 (0.7) 1.0 (0.7) 1.5 (0.7) 1.5 (0.7)
Tender joints 30.1 (14.1) 29.1 (13.3) 13.6 (7.7) 14.6 (9.2) 24.1 (16.2) 8.8 (12.4) 9.1 (12.8) 25.4 (15.3) 26.3 (15.8)
Swollen joints 20.4 (9.6) 19.4 (8.6) 10.5 (5.4) 10.6 (5.4) 17.2 (12.1) 4.3 (5.9) 5.4 (6.4) 15.8 (9.8) 15.9 (10.0)
RF positive, % 84.8 85.9 85.0 86.1 67.0 NR NR 75.5 77.4

Data are mean (s.d.), unless otherwise stated. aData are presented for patients treated in period II; baseline is the start of period I. NR: not reported; VAS: visual analogue scale. bPatient recruited from the AIM study (Abatacept in Inadequate Responders to Methotrexate). cPatients recruited from the ATTAIN study (Abatacept Trial in Treatment of Anti-TNF Inadequate responders).