Evidence map›Paper›PMID 36829225›Full record

SynthesisPediatric rheumatology online journal2023

Efficacy and safety of TNF inhibitors in the treatment of juvenile idiopathic arthritis: a systematic literature review.

Gerd Horneff, Kirsten Minden, Catherine Rolland, Ana C Hernandez Daly, Cecilia Borlenghi, Nicolino Ruperto

Open access · goldAbstract readSystematic Review
In one paragraph

Synthesis in Pediatric rheumatology online journal, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
4.4field-weighted citation impact, top 5% of its field
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

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 15 citations in OpenAlex.

  1. Tumor necrosis factor (TNF) inhibitors for juvenile idiopathic arthritis.The Cochrane database of systematic reviews · 2025
    Pooled it
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Review
  8. Juvenile idiopathic arthritis and associated uveitis: A review of pathogenesis, diagnosis, and management.Saudi journal of ophthalmology : official journal of the Saudi Ophthalmological Society
    Article
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

6 authors at 3 institutions in 2 countries.

Gerd Horneff *Department of General Paediatrics, Asklepios Clinic Sankt Augustin, Sankt Augustin, Germany. g.horneff@asklepios.com.ORCID http://orcid.org/0000-0001-5491-7832
Kirsten Minden *German Rheumatism Research Centre Berlin (DRFZ), Leibniz Association, Berlin, Germany.
Catherine RollandCuro Consulting, Envision Pharma Group, Glasgow, UK.
Ana C Hernandez DalyPfizer, Athens, Greece.
Cecilia BorlenghiPfizer, Buenos Aires, Argentina.
Nicolino RupertoIRCCS Istituto Giannina Gaslini, UOSID Centro Trial, Genoa, Italy.
Asklepios Klinik Sankt Augustin · DEIstituto Giannina Gaslini · ITLeibniz Association · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveA systematic literature review was conducted to summarize efficacy and safety data from studies that evaluated tumor necrosis factor inhibitors in patients with juvenile idiopathic arthritis (JIA).

methodsRelevant publications were identified via online searches (cutoff: March 16, 2021). After screening search results, outcome data were extracted if the treatment arm included ≥ 30 patients. Outcomes were described narratively, with efficacy assessed by JIA-American College of Rheumatology (ACR) response criteria and safety assessed by the incidence of serious adverse events (SAEs) per 100 patient-years (100PY).

resultsAmong 87 relevant publications included in the qualitative synthesis, 19 publications described 13 clinical trials. Across the 13 trials, the percentages of patients who achieved JIA-ACR30/50/70/90 responses at Week 12 with adalimumab ranged 71-94%, 68-90%, 55-61%, and 39-42%, respectively; with etanercept (Week 12), 73-94%, 53-78%, 36-59%, and 28%; with golimumab (Week 16), 89%, 79%, 66%, and 36%; and with infliximab (Week 14), 64%, 50%, and 22% (JIA-ACR90 not reported). SAE incidence across all time points ranged 0-13.7 SAE/100PY for adalimumab, 0-20.0 SAE/100PY for etanercept, and 10.4-24.3 SAE/100PY for golimumab (1 study). SAE incidence could not be estimated from the 2 infliximab publications.

conclusionTumor necrosis factor inhibitors are effective and well tolerated in the treatment of JIA, but additional evidence from head-to-head studies and over longer periods of time, especially in the context of the transition from pediatric to adult care, would be useful.

Indexed as

Antirheumatic AgentsArthritis, JuvenileTransition to Adult CareAdalimumabAdultAntibodies, Monoclonal, HumanizedChildEtanerceptHumansInfliximabTreatment OutcomeTumor Necrosis Factor-alphaTumor Necrosis Factor InhibitorsAdalimumabAntibodies, Monoclonal, HumanizedAntirheumatic AgentsEtanerceptInfliximabTumor Necrosis Factor-alphaTumor Necrosis Factor Inhibitors

Identifiers

PMID36829225
PMCPMC9951426
OpenAlexW4321785380

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.