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Table 1 Algorithm for treat-to-target disease-modifying anti-rheumatic drug (DMARD) therapy

From: Characterising deviation from treat-to-target strategies for early rheumatoid arthritis: the first three years

Follow up, weeks*

DMC fulfilled 1

Medications

Methotrexate (MTX)

Hydroxychloroquine (HCQ)

Sulfasalazine (SSZ)

Other DMARDs

0

 

10 mg/wk oral2

400 mg/d

0.5 g/d to 2.0 g/d3

 

6

Yes

10 mg/wk oral2

400 mg/d

3.0 g/d

 

12

Yes

15 mg/wk oral2

400 mg/d

3.0 g/d

 

18

Yes

20 mg/wk oral2

400 mg/d

3.0 g/d

 

24

Yes

25 mg/wk oral4

400 mg/d

3.0 g/d

 

30

Yes

25 mg/wk inj

400 mg/d

3.0 g/d

LFN 10 mg#

36

Yes

25 mg/wk inj

400 mg/d

3.0 g/d

LFN 20 mg

42

Yes

25 mg/wk inj

400 mg/d

3.0 g/d

LFN 20 mg + gold inj 50 mg/wk

48

Yes

25 mg/wk inj

400 mg/d

3.0 g/d

LFN 20 mg + gold inj 50 mg/wk + Cyclosporine A 2.5 mg/kg5#

54

Yes

25 mg/wk inj

400 mg/d

3.0 g/d

LFN 20 mg + gold inj 50 mg/wk + Cyclosporine A 3 mg/kg

60

Yes

25 mg/wk inj

400 mg/d

3.0 g/d

LFN 20 mg + gold inj 50 mg/wk + Cyclosporine A 4 mg/kg#

66

Yes

25 mg/wk inj

400 mg/d

3.0 g/d

LFN 20 mg + gold inj 50 mg/wk + Cyclosporine A 4 mg/kg + azathioprine 1-2 mg/kg#

72

Yes

If an inadequate response has occurred after 3 months, treatment failure

  1. *Patients were reviewed at least every 6 weeks and therapy was increased if the treatment target had not been reached. Weeks of follow up are listed in the case of continued disease activity and hence increase in therapy at every visit. #Biological DMARDs can be added, if Pharmaceutical Benefits Scheme criteria are fulfilled. 1If dose modification criteria (DMC) are not fulfilled, treatment is not modified; 2MTX administered parenterally if gastrointestinal side effects, 3starting dose 0.5 g/d and then increased by 0.5 g/d at weekly intervals to 2 g/d; 4maximum dose of MTX was based on weight and renal function: if weight <50 kg and/or creatinine clearance >30 but <60, MTX 20 mg/wk orally or parenterally, and if weight >50 kg and creatinine clearance >60 ml/min, MTX 25 mg/kg orally or parenterally. DMC, dose modification criteria; LFN, leflunomide; inj, injection.