Characteristics of studies including biomarkers studied >2 times
Author | Design | Patient selection | Biological | Medication history | Duration of follow-up | Response criteria | Biomarker(s) studied |
Abhishek et al20 | Monocentre retrospective case–control study | DAS28 ≥5.1 on 2 separate occasions a month apart | Adalimumab, etanercept, infliximab | Failure of ≥2 DMARDs including MTX, biological naïve | 3 months | EULAR | RF |
Avila-Petretti et al34 | Multicentre prospective cohort | ≥1 erosions in ≥2 joint groups in hands and/or feet | Adalimumab, etanercept, infliximab | Biological naïve | 12 weeks | EULAR | FcGR2A |
Blaschke et al 11 | Monocentre prospective cohort | ≥3 TJC, ≥3 SJC, VAS pain ≥40 mm, morning stiffness for >1 hour, ESR >28 mm/hour or CRP >8 mg/L | Etanercept | Failure to MTX or leflunomide | 24 weeks | EULAR | RF, anti-CCP |
Cañete et al33 | Two-centre prospective cohort | Non-responsive to DMARD therapy, not further specified | Infliximab | Failure to MTX | 30 weeks | EULAR | FcGR2A |
Choi et al12 | Two prospective cohorts from same centre | DAS28 ≥3.2 | Adalimumab, infliximab | Failure of ≥1 DMARD including MTX | 16 weeks | EULAR | RF, anti-CCP |
Cuchacovich et al28 | Monocentre prospective cohort | ≥6 SJC, ≥9 TJC and morning stiffness ≥45 min | Adalimumab | Failure of leflunomide, MTX or sulfasalazine | 24 weeks | ΔDAS >1.2 | TNF-α (−308) |
Davila-Fajardo et al32 | Registry data | DAS28 ≥3.2 | Adalimumab | Failure of ≥2 DMARDs including MTX | 14 weeks | EULAR* | FcGR2A |
Guis et al23 | Two-centre prospective cohort | DAS28 ≥3.2 | Etanercept | Some used MTX or infliximab previously | 24 weeks | ΔDAS >1.2 | TNF-α (−308) |
Hyrich et al22 | Registry data | DAS28 ≥5.1 | Etanercept, infliximab | Failure of ≥2 DMARDs including MTX | 24 weeks | EULAR | RF |
Jančić et al27 | Monocentre prospective cohort | Start of TNFi, not further specified | Etanercept | Not specified | 6 months | ΔDAS >1.2 | TNF-α (−308) |
Kang et al30 | Monocentre prospective cohort | >6 TJC and/or SJC and ESR >28 mm/hour, CRP >2.0 mg/dL or morning stiffness ≥45 min | Etanercept | Failure of ≥1 DMARD including MTX, biological naïve | 12 weeks | ACR20 | HLA-DRB1 |
Klaasen et al13 | Prospective cohort | DAS28 ≥3.2 | Infliximab | Failure to MTX | 16 weeks | ΔDAS >1.2 | RF, anti-CCP |
Lequerré et al16 | Prospective cohort | ≥3 of: ≥3 SJC, ≥6 TJC, morning stiffness ≥45 min, ESR >22 mm/hour, CRP >20 mg/L | Infliximab | Failure of ≥1 DMARD including MTX | 14 weeks | EULAR | RF |
Marotte et al24 | Multicentre prospective cohort | Active disease, not further specified | Infliximab | Failure to MTX | 30 weeks | ACR20 | HLA-DRB1 |
Matsudaira et al17 | Monocentre cohort | Start of TNFi, not further specified | Adalimumab, etanercept, infliximab | Biological naïve | 24 weeks | EULAR | Anti-CCP |
Miceli-Richard et al29 | Multicentre prospective cohort | DAS28 ≥3.2 | Adalimumab | Failure of ≥1 DMARD | 12 weeks | ACR50 | TNF-α (−308), HLA-DRB1 |
Morales-Lara et al21 | Two-centre prospective cohort | Start of TNFi, not further specified | Adalimumab, etanercept, infliximab | Biological naïve | 6 months | EULAR | RF |
Mugnier et al25 | Monocentre prospective cohort | DAS28 >3.2 | Infliximab | Failure to MTX (≥2 months) | 22 weeks | ΔDAS>1.2 | TNF-α (−308) |
Padyukov et al26 | Two-centre prospective cohort | Start of TNFi, not further specified | Etanercept | Failure of ≥1 DMARD | 12 weeks | EULAR | TNF-α (−308) |
Pers et al14 | Monocentre retrospective cohort | Not specified | Adalimumab, etanercept, infliximab | Not specified | 24 weeks | EULAR | Anti-CCP |
Salgado et al19 | Multicentre retrospective cohort | Not specified | Adalimumab, etanercept, infliximab | Not specified | 24 weeks | EULAR | RF |
Skapenko et al31 | Multicentre, double-blind. randomised controlled trial | DAS28 >3.2. SJC66 ≥6, TJC68 ≥8, ESR >28 mm/hour, CRP >1.5 mg/dL, >1 hand/feet erosion by X-ray | Adalimumab | MTX and TNFi naïve | 26 weeks | DAS28 <3.2 | HLA-DRB1 |
Wampler Muskardin et al15 | Registry data | Start of TNFi, not further specified | Adalimumab, certolizumab pegol, etanercept, golimumab, infliximab | Not specified | 12 weeks | EULAR | Anti-CCP |
Zhao et al18 | Monocentre prospective cohort | DAS28 ≥3.2 | Etanercept | Failure of ≥1 DMARD including MTX and/or leflunomide (≥3 months) | 12 weeks | EULAR | RF, anti-CCP |
*EULAR good response versus moderate+non-responders.
ACR, American College of Rheumatology; CCP, cyclic citrullinated peptide; CRP, C reactive protein; DAS28, Disease Activity Score based on 28-joint count; DMARD, disease-modifying antirheumatic drug; ESR, erythrocyte sedimentation rate; EULAR, European Alliance of Associations for Rheumatology; MTX, methotrexate; RF, rheumatoid factor; SJC, swollen joint count; TJC, tender joint count; TNFi, tumour necrosis factor inhibitor; VAS, Visual Analogue Scale.