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Table 3 Proportion of patients who achieved therapy effectiveness and individual criteria at 1 year of follow-up (n = 16,305)

From: Effectiveness and safety of tofacitinib in rheumatoid arthritis: a cohort study

Effectiveness criteria

DMARDs

TNFi ± DMARDs

Non-TNF biologics ± DMARDs

Tofacitinib ± DMARDs

Percent

95% CI

Percent

95% CI

Percent

95% CI

Percent

95% CI

Effective therapy (satisfied all six criteria)

11.1

10.1–12.1

18.6

17.9–19.4

19.8

18.2–21.4

15.4

6.6–24.2

Criterion 1

High adherence

26.6

25.1–28.0

44.0

43.0–44.9

53.3

51.3–55.3

27.7

16.8–38.6

Criterion 2

No biologic or tofacitinib switch or addition

72.7

71.2–74.1

64.3

63.4–65.2

82.1

80.5–83.6

84.6

75.8–93.4

Criterion 3

No DMARD switch or addition

85.3

84.2–86.5

96.1

95.8–96.5

95.5

94.6–96.3

98.5

95.5–100

Criterion 4

No increase in dose or frequency of index drug

92.0

91.1–92.9

94.0

93.5–94.4

88.9

87.6–90.1

100.0a

Criterion 5

No more than one glucocorticoid joint injection

91.3

90.3–92.2

88.8

88.2–89.4

72.8

71.0–74.6

87.7

79.7–95.7

Criterion 6

No new/increased oral glucocorticoid dose

81.4

80.2–82.7

83.3

82.6–84.1

78.0

76.3–79.7

76.9

66.7–87.2

  1. DMARD Disease-modifying antirheumatic drug, TNFi Tumor necrosis factor inhibitors
  2. aStandard tofacitinib dose is usually not increased