Evidence map›Paper›PMID 40393718›Full record

SynthesisThorax2025

Systematic review and meta-analysis of the efficacy of biologic and targeted synthetic therapies in sarcoidosis.

Katie Bechman, Kathryn Biddle, Aitana Miracle, Kelly He, Mark Gibson, Mark D Russell, Sarah Walsh, Peter Brex, Amit S Patel, Katherine J Myall and 3 more

Abstract readSystematic ReviewMeta-Analysis
In one paragraph

Synthesis in Thorax, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed.

  1. Review
  2. Article
  3. Quality of Life in Sarcoidosis.Diagnostics (Basel, Switzerland) · 2026
    Review
  4. Advances in management of sarcoidosis-associated fatigue: A narrative review.Sarcoidosis, vasculitis, and diffuse lung diseases : official journal of WASOG · 2026
    Article
  5. New Therapies for Sarcoidosis: Molecular and Pathophysiological Basis.International journal of molecular sciences · 2026
    Review
  6. Review
  7. Contemporary management of sarcoidosis.Frontiers in medicine · 2026
    Review
  8. Article
  9. Review
  10. Article
  11. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors.

Katie BechmanCentre for Rheumatic Diseases, King's College London, London, UK katie.bechman@kcl.ac.uk.ORCID 0000-0001-7552-0463
Kathryn BiddleCentre for Rheumatic Diseases, King's College London, London, UK.
Aitana MiracleCentre for Rheumatic Diseases, King's College London, London, UK.
Kelly HeCentre for Rheumatic Diseases, King's College London, London, UK.
Mark GibsonCentre for Rheumatic Diseases, King's College London, London, UK.
Mark D RussellCentre for Rheumatic Diseases, King's College London, London, UK.
Sarah WalshDepartment of Dermatology, King's College Hospital NHS Foundation Trust, London, UK.
Peter BrexDepartment of Neurology, King's College Hospital NHS Foundation Trust, London, UK.
Amit S PatelAsthma, Allergy and Lung Biology, King's College London, London, UK.
Katherine J MyallAsthma, Allergy and Lung Biology, King's College London, London, UK.
Sam NortonDepartment of Psychology, King's College London, London, UK.
Surinder S BirringAsthma, Allergy and Lung Biology, King's College London, London, UK.
James GallowayCentre for Rheumatic Diseases, King's College London, London, UK.ORCID 0000-0002-1230-2781

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesInfliximab, an anti-TNF agent, is used to treat sarcoidosis that does not respond to corticosteroids or second-line agents. The efficacy of other anti-TNF agents, non-TNF biologics and targeted synthetic therapies remains unclear. This study aims to evaluate the role of these therapies in the management of multisystem sarcoidosis.

methodsWe conducted a systematic literature search to identify trials of biological and targeted synthetic therapies in sarcoidosis. Meta-analyses examined %-predicted forced vital capacity (FVC), as mean change from baseline. Heterogeneity was measured using the I

resultsThe search identified 6777 records. Sixteen studies met the inclusion criteria. These included 8 randomised control trials (RCTs) and 8 single-arm trials. Fourteen studies evaluated biologic therapies: infliximab (n=5), adalimumab (n=2), etanercept (n=2), golimumab (n=1), rituximab (n=1), anakinra (n=1), sarilumab (n=1), ustekinumab (n=1) and efzofitimod (n=1). Two trials assessed the targeted synthetic therapy tofacitinib. Risk of bias was high in five of eight RCTs. Meta-analysis of %-predicted FVC showed modest improvement with treatment (mean change: 4.79% (95% CI 1.22 to 8.35), driven by anti-TNF trials 5.70% (95% CI 1.61 to 9.78). Heterogeneity was substantial (I²=76.3%). In data synthesis using vote counting, infliximab, adalimumab, efzofitimod and tofacitinib demonstrated a positive direction of effect across all estimates, though improvements in several outcomes did not reach thresholds for minimal clinically important differences.

conclusionsMeta-analysis supports infliximab use in pulmonary sarcoidosis, although improvements in lung function are modest. There is limited but promising evidence for the use of adalimumab and tofacitinib in cutaneous disease and efzofitimob in pulmonary disease. Study interpretation is limited by small sample sizes and heterogeneity in study design and population.PROSPERO registration numberCRD42024599560.

Indexed as

Biological ProductsSarcoidosisAdalimumabHumansInfliximabTreatment OutcomeAdalimumabBiological ProductsInfliximabSarcoidosis

Identifiers

PMID40393718
PMCPMC12505053

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.