Table 1.
Basic characteristics of included studies
Author | Year | Country/region | Mean age (years) | Disease duration at anakinra start | Treatment arm | Study duration | Study quality score |
---|---|---|---|---|---|---|---|
Lequerré et al28 | 2008 | France | 38.1 | 7.8 years† | Anakinra 100 mg/day | 17.5 months† | 6 |
Nordström et al29 | 2012 | Europe* | 39 39 |
14 months‡ 19 months‡ |
Anakinra 100 mg/day DMARD treatment# |
24 weeks 24 weeks |
8 |
Cavalli et al30 | 2013 | Italy | – | 5 years† | Anakinra 100 mg/day | At least 24 months | 4 |
Gerfaud-Valentin et al13 | 2014 | France | 36 | 4 months‡ | Anakinra 100 mg/day | 27.8 months† | 7 |
Giampietro et al31 | 2013 | France | 33.3 | 9.3 years† | Anakinra 100 mg/day | 23 months† | 6 |
Laskari et al32 | 2011 | Greece | 32 | 7 months‡ | Anakinra 100 mg/day | 15 months‡ | 6 |
Iliou et al33 | 2013 | Greece | 38.3 | 3.5 months† | Anakinra 100 mg/day | 7 years‡ | 6 |
Giampietro et al34 | 2010 | France | 40.6 | 9.4 years† | Anakinra 100 mg/day | 30.7 months† | 5 |
Notes:
Patients in Finland, Norway, and Sweden were included for study.
Mean time.
Median time.
Six patients with methotrexate (10–25 mg weekly, oral), three patients with azathioprine (1–3 mg/kg/day, oral), and one patient with leflunomide (20 mg/day, oral).
Abbreviation: DMARD, disease-modifying antirheumatic drugs.