Evidence map›Paper›PMID 35907978›Full record

ArticlePediatric rheumatology online journal2022

Latent classes of early response trajectories to biologics initiation in juvenile idiopathic arthritis: an analysis of four trials.

Lily Siok Hoon Lim, Shamsia Shobhan, Armend Lokku, Sarah Ringold, Eleanor Pullenayegum

3 registry-linked trialsAbstract read
In one paragraph

Article in Pediatric rheumatology online journal, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 3 registered trials, which are not on this map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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.

NCT00095173 phase3completednot on this map

A Phase III, Multi-Center, Multi-National, Randomized Withdrawal Study to Evaluate the Safety and Efficacy of BMS-188667 in Children and Adolescents With Active Polyarticular Juvenile Rheumatoid Arthritis (JRA)

TypeinterventionalSponsorBristol-Myers SquibbRan2003 to 2011Enrolled214ConditionsJuvenile Rheumatoid ArthritisArmsAbatacept, Placebo
NCT00443430 phase4completednot on this map

Trial of Early Aggressive Therapy in Juvenile Idiopathic Arthritis (TREAT in JIA)

TypeinterventionalSponsorSeattle Children's HospitalRan2007 to 2010Enrolled85ConditionsJuvenile Chronic Polyarthritis, Juvenile Idiopathic Arthritis, Juvenile Rheumatoid ArthritisArmsmethotrexate, methotrexate - etanercept - prednisolone arm
NCT00988221 phase3completednot on this map

A 24 Week Randomized, Double-blind, Placebo-controlled Withdrawal Trial With a 16 Week Open-label lead-in Phase, and 64 Week Open-label Follow-up, to Evaluate the Effect on Clinical Response and the Safety of Tocilizumab in Patients With Active Polyarticular-course Juvenile Idiopathic Arthritis

TypeinterventionalSponsorHoffmann-La RocheRan2009 to 2013Enrolled188ConditionsJuvenile Idiopathic ArthritisArmsTocilizumab, Placebo
3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Trial
  2. Article
  3. Article
  4. 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

5 authors.

Lily Siok Hoon LimDepartment of Pediatrics, Children's Hospital Research Institute of Manitoba, University of Manitoba, 501F-715 McDermot Ave, Winnipeg, Manitoba, R3E 0V9, Canada. llim@chrim.ca.ORCID http://orcid.org/0000-0002-0675-0668
Shamsia ShobhanDepartment of Community Health Sciences, University of Manitoba, Winnipeg, Canada.
Armend LokkuDalla Lana School of Public Health, University of Toronto, Toronto, Canada.
Sarah RingoldSeattle Children's Hospital, Seattle, USA.
Eleanor PullenayegumDalla Lana School of Public Health, University of Toronto, Toronto, Canada.

Funding

Arthritis Foundation 319804CARRA 319804
6 · The paper itself

Abstract

aims1) To delineate latent classes of treatment response to biologics in juvenile idiopathic arthritis (JIA) patients in the first 16 weeks after initiation. 2) To identify predictors of early disease response.

methodsThe study population was drawn from four biologics trials in polyarticular course JIA: Etanercept 2000, Abatacept 2008, TRial of Early Aggressive Therapy (TREAT) 2012 and Tocilizumab 2014. The outcome was active joint counts (AJC). Semiparametric latent class trajectory analysis was applied to identify latent classes of response to treatment; AJC was transformed for this modelling. We tested baseline disease and treatment characteristics for their abilities to predict class membership of response.

resultsThere were 480 participants, 74% females. At baseline, 26% were rheumatoid factor positive. 67% were on methotrexate at enrollment. Three latent class solution provided the best fit. Baseline AJC was the sole best predictor of class membership. Participants classified by their highest membership probabilities into high baseline AJC (> 30) and slow response (26.5%), low baseline AJC (< 10), early and sustained response (29.7%), and moderate baseline AJC progressive response (43.8%). Participants were classified into the latent classes with a mean class membership posterior probability of 0.97. Those on methotrexate at baseline were less likely to belong to high baseline AJC class.

conclusionsThree latent classes of responses were detectable in the first 16 weeks of biologics therapy. Those with the highest baseline AJC demonstrated very slow response in this window and were less likely to be on concomitant methotrexate. TRIALS REGISTRATION: TREAT 2012 (NCT NCT00443430 ) (Wallace et. al, Arthritis Rheum 64:2012-21, 2012), tocilizumab trial 2014 ( NCT00988221 ), abatacept trial 2008 ( NCT00095173 ). Etanercept 2000 from Amgen does not have a trial registration number.

Indexed as

Antirheumatic AgentsArthritis, JuvenileBiological ProductsAbataceptEtanerceptFemaleHumansMaleMethotrexateTreatment OutcomeAbataceptAntirheumatic AgentsBiological ProductsEtanerceptMethotrexateBiologicsDisease activity trajectoryJuvenile idiopathic arthritisPolyarticular-courseResponseTreatmentTrials

Identifiers

PMID35907978
PMCPMC9338501

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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.