Table 1.

Patients’ baseline characteristics.

CharacteristicNonresponse (A) n = 49Loss of Response (B) n = 75Adverse Events (C) n = 73p
Female (%)29 (59.2)46 (75.3)55 (75.3)0.101
Age, yrs, mean (SD)54 (12)55 (12)55 (12)0.970
Disease duration, yrs, median (range)6 (0.7–37)7 (1–55)10 (0.5–46)0.074
RF-positive (%)41 (83.7)56 (74.7)54 (74)0.405
No. previous DMARD, median (range)*3 (2–10)3 (1–8)4 (1–9)0.463
DAS28 at baseline 2nd anti-TNF agent, mean (SD)5.8 (1.1)4.9 (1.1)4.8 (1.3)< 0.0001
1st anti-TNF agent used
  Infliximab (%)18 (36.7)29 (38.7)44 (60.3)0.010
  Etanercept (%)16 (32.7)27 (36.0)12 (16.4)0.021
  Adalimumab (%)15 (30.6)19 (25.3)17 (23.3)0.657
2nd anti-TNF agent used
  Infliximab (%)2 (4.1)2 (2.7)1 (1.4)0.644
  Etanercept (%)30 (61.2)34 (45.3)45 (61.6)0.086
  Adalimumab (%)17 (34.7)39 (52)27 (37)0.086
Switch of therapy
  Antibody to receptor blocker (%)30 (61.2)34 (45.3)45 (61.6)0.086
  Receptor blocker to antibody (%)16 (32.7)27 (36)12 (16.4)0.021
  Antibody to antibody (%)3 (6.1)14 (18.7)16 (22)0.062
Concurrent medication 2nd anti-TNF agent used**
  MTX (%)23 (46.9)41 (54.7)28 (38.4)0.138
  Other DMARD (%)7 (14.3)21 (28.0)19 (26.0)0.186
  Corticosteroids (%)28 (57.1)27 (36)16 (21.9)< 0.0001
  • * Missing data in 2% (1/49) in A.

  • ** Missing data in A, B, and C, 14% (7/49), 9% (7/75), and 16% (12/73), respectively. RF: rheumatoid factor; DMARD: disease modifying antirheumatic drugs; TNF: tumor necrosis factor; MTX: methotrexate.