Table 1.

Patient demographics and baseline characteristics.

CharacteristicTofacitinib All (5 and 10 mg BID ± background DMARD), n = 4102*Tofacitinib 5 mg BID ± background DMARD, n = 1421Tofacitinib 10 mg BID ± background DMARD, n = 2681Tofacitinib 5 and 10 mg BID + background DMARD, n = 2742Tofacitinib 5 and 10 mg BID monotherapy, n = 1360
Total patient-yrs of exposure59633215274836842279
Mean (maximum) duration of treatment/exposure, days531 (1844)826 (1844)374 (1353)491 (1822)612 (1844)
Sex, n (%)
  Male696 (17.0)235 (16.5)461 (17.2)479 (17.5)217 (16.0)
  Female3406 (83.0)1186 (83.5)2220 (82.8)2263 (82.5)1143 (84.0)
Mean age, yrs (SD)53.2 (11.5)52.8 (11.9)53.4 (11.3)53.4 (11.5)52.8 (11.6)
Race, n (%)
  White2330 (56.8)648 (45.6)1682 (62.7)1652 (60.2)678 (49.9)
  Black110 (2.7)22 (1.5)88 (3.3)75 (2.7)35 (2.6)
  Asian1087 (26.5)624 (43.9)463 (17.3)679 (24.8)408 (30.0)
  Hispanic14 (0.3)14 (1.0)012 (0.4)2 (0.1)
  Other312 (7.6)106 (7.5)206 (7.7)206 (7.5)106 (7.8)
  Unspecified249 (6.1)7 (0.5)242 (9.0)118 (4.3)131 (9.6)
Mean weight, kg (SD)70.2 (19.2)65.5 (17.1)72.9 (19.9)71.1 (19.5)68.2 (18.5)
BMI, kg/m2 (SD)26.7 (6.4)25.4 (5.8)27.4 (6.6)26.9 (6.5)26.1 (6.1)
  • * Baseline values were available for 3783 patients (92.2%) from the index study; 319 patients (7.8%) had new baseline values derived from the last pre-drug visit on entry to the LTE studies, or were missing baseline values as of the data cutoff.

  • Excluding white, black, Asian, and Hispanic patients.

  • Race was not provided by patients. BID: twice daily; BMI: body mass index; DMARD: disease-modifying antirheumatic drug.