Table 2.

Baseline disease characteristics and medication use by therapy type and by route of MTX administration.

CharacteristicsMonotherapy, n = 153Combination Therapy, n = 661Total, n = 814pOral MTX, n = 285SC MTX, n = 230Total, n = 515p
Disease characteristics
  Disease duration, yrs, mean (SD)12.3 (10.0)8.8 (9.9)9.4 (10.0)< 0.0001*8.7 (9.9)7.9 (9.5)8.3 (9.8)0.32
  Early RA, n (%)16 (10.5)134 (20.3)150 (18.4)0.004*63 (22.1)50 (21.7)113 (21.9)0.92
  Ever presence of erosion, n (%)
    Yes79 (51.6)314 (47.5)393 (48.3)0.002*128 (44.9)115 (50.0)243 (47.2)0.17
    Unsure23 (15.1)63 (9.5)86 (10.6)33 (11.6)16 (7.0)49 (9.5)
    Missing12 (10.3)41 (6.5)53 (7.0)26 (9.1)20 (8.7)46 (8.9)
  RF-positive, n (%)
    Yes106 (69.3)456 (69.0)562 (69.0)0.20202 (70.9)159 (69.1)361 (70.1)0.17
    Missing19 (12.4)43 (6.5)62 (7.7)24 (8.4)9 (3.9)33 (6.4)
  Swollen joint count (0–28), mean (SD)§8.2 (5.8)7.0 (5.0)7.2 (5.2)0.02*6.8 (5.1)6.6 (4.4)6.7 (4.8)0.61
  Tender joint count (0–28), mean (SD)7.5 (6.3)7.6 (7.0)7.6 (6.6)0.907.8 (6.7)6.9 (5.8)7.4 (6.3)0.12
  DAS28-ESR, mean (SD)††4.8 (1.4)4.7 (1.4)4.7 (1.4)0.644.7 (1.4)4.6 (1.4)4.7 (1.4)0.45
  PGA (1–10), mean (SD)‡‡4.9 (2.5)4.8 (2.4)4.8 (2.4)0.714.8 (2.5)4.8 (2.4)4.8 (2.4)0.91
  PtGA (1–10), mean (SD)§§5.8 (2.8)5.5 (2.6)5.6 (2.7)0.325.5 (2.6)5.4 (2.7)5.4 (2.6)0.69
  HAQ-DI (0–3), mean (SD)¶¶1.5 (0.7)1.3 (0.7)1.4 (0.8)0.05*1.3 (0.7)1.3 (0.7)1.3 (0.7)0.81
  No. comorbidities, mean (SD)†††3.3 (2.1)2.7 (2.0)2.8 (2.0)0.001*2.7 (1.9)2.6 (2.0)2.6 (1.9)0.49
Medication use
  Prior use of csDMARD, n (%)147 (96.1)601 (90.9)748 (91.9)0.43264 (92.6)204 (88.7)468 (90.9)0.12
  Prior use of bDMARD, n (%)75 (49.0)193 (29.2)268 (32.9)< 0.0001*87 (30.5)57 (24.8)144 (27.9)0.14
  Type of bDMARD, n (%)
    Non-TNFi36 (23.5)102 (15.4)138 (17.0)0.02*37 (13.0)36 (15.7)73 (14.2)0.39
    TNFi117 (76.5)559 (84.6)676 (83.0)248 (87.0)194 (84.3)442 (85.8)
  Use of MTX at start of bDMARD, n (%)NA515 (78.0)515 (66.3)NA285 (100)230 (100)515 (100)NA
  Additional use of csDMARD in MTX users, n (%)
    At least 1 csDMARD other than MTXNA258 (50.1)‡‡‡258 (50.1)‡‡‡NA144 (50.5)114 (49.6)258 (50.1)0.14
    HydroxychloroquineNA163 (31.7)‡‡‡163 (31.7)‡‡‡NA87 (30.5)76 (33.0)163 (31.7)0.54
    LeflunomideNA108 (21.0)‡‡‡108 (21.0)‡‡‡NA62 (21.8)46 (20.0)108 (21.0)0.63
    SulfasalazineNA72 (14.0)‡‡‡72 (14.0)‡‡‡NA34 (11.9)38 (16.5)72 (14.0)0.14
    OtherNA8 (1.6)‡‡‡8 (1.6)‡‡‡NA4 (1.4)4 (1.7)8 (1.6)0.76
  MTX administration route, n (%)‡‡‡
    OralNA285 (55.3)285 (55.3)NA285 (100)0 (0.0)285 (55.3)NA
    SCNA230 (44.7)230 (44.7)0 (0.0)230 (100)230 (44.7)NA
  MTX dose, mg/week, mean (SD)18.8 (6.0)20.7 (5.6)19.7 (5.9)0.0003*
  MTX dose category, mg/week, n = 498
    ≤ 1581 (28.4)47 (20.4)128 (24.9)< 0.0001*
    15–20148 (51.9)71 (30.9)219 (42.5)
    > 2056 (19.7)112 (48.7)168 (32.6)
  • * Statistically significant p value.

  • Disease duration ≤ 1 year.

  • § Available n = 682 (435 for MTX users).

  • Available n = 671 (429 for MTX users).

  • †† Available n = 586 (374 for MTX users).

  • ‡‡ Available n = 618 (398 for MTX users).

  • §§ Available n = 615 (397 for MTX users).

  • ¶¶ Available n = 583 (367 for MTX users).

  • ††† Available n = 765 (483 for MTX users).

  • ‡‡‡ Proportions based on the no. MTX users (n = 515). DAS28-ESR: 28-joint count Disease Activity Score using erythrocyte sedimentation rate; csDMARD: conventional synthetic disease-modifying antirheumatic drugs; bDMARD: biologic DMARD; HAQ-DI: Health Assessment Questionnaire–Disability Index; MTX: methotrexate; NA: not available; PGA: physician’s global assessment; PtGA: patient’s global assessment; RA: rheumatoid arthritis; RF: rheumatoid factor; SC: subcutaneous; TNFi: tumor necrosis factor inhibitor.