Rheumatoid arthritis

Effects of biologic and targeted synthetic disease modifying antirheumatic drugs (b/tsDMARDs) on patient-reported outcome domains in rheumatoid arthritis: a systematic review and network meta-analyses

RMD OpenPublished Systematic review and network meta-analysis of randomised trials

Study context

Population
Patients with rheumatoid arthritis (RA) in RCTs comparing DMARDs with placebo or other DMARDs and reporting patient-reported outcomes (PROs) from the International Consortium for Health Outcomes Measurement (ICHOM) standard set for inflammatory arthritis99 studies
Comparison
b/tsDMARD classes compared with each other on PROs
Outcome
Relative effects of b/tsDMARDs on ICHOM RA-relevant PRO domains: pain, fatigue, activity limitation, and physical and mental health
Methodological detailsrandom-effects network meta-analysis (NMA), machine learning literature search (ASReview)
  • Random-effects NMA
  • Machine learning literature search (ASReview)

Pooled result

As reported in the abstract

Activity limitation (HAQ), MD
Significantly better at reducing activity limitation
MD (95% CI)
JAKivs TNFi
−0.13(−0.23 to −0.04)
IL-6 inhibitorsvs TNFi
−0.13(−0.27 to −0.00)

Further pooled results

Mental health domain ranking — IL-6 inhibitors
82%
Mental health domain ranking — IL-6 inhibitors ranked highest in the mental health domain
82%

Overall ranking (surface under the cumulative ranking curve)

Rituximab overall ranked best among b/tsDMARDs

Predictors of PRO improvement

Early RA (<3 years diagnosis) and worse baseline PRO scores associated with larger PRO improvements
P < 0.05

Original publication

Effects of biologic and targeted synthetic disease modifying antirheumatic drugs (b/tsDMARDs) on patient-reported outcome domains in rheumatoid arthritis: a systematic review and network meta-analyses. RMD Open. Published 24 June 2026. doi:10.1136/rmdopen-2025-006578

Composed by AI from the published abstract and checked against it. How Briefs are made →

Get them every week

New studies on this topic in My Week and in your Monday e-mail.

We e-mail you a sign-in link and a code. No password, no spam.