Evidence map›Paper›PMID 31714580›Full record

ArticleRheumatology (Oxford, England)2020

Early response to anti-TNF predicts long-term outcomes including sustained remission: an analysis of the BSRBR-RA.

Philip D H Hamann, John D Pauling, Neil McHugh, Kimme Hyrich, Gavin Shaddick, BSRBR-RA Contributors Group

Abstract read
In one paragraph

Article in Rheumatology (Oxford, England), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Trial
  2. Observational
  3. Review
  4. Observational
  5. Article
  6. Article
  7. Article
  8. Article
  9. Long-term response in RA apparent by 6 months.Nature reviews. Rheumatology · 2020
    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.

Philip D H HamannMusculoskeletal Research Unit, University of Bristol, Bristol.
John D PaulingDepartment of Pharmacy and Pharmacology, University of Bath, Bath.
Neil McHughDepartment of Pharmacy and Pharmacology, University of Bath, Bath.
Kimme HyrichDivision of Musculoskeletal and Dermatological Sciences, University of Manchester, Manchester.
Gavin ShaddickDepartment of Mathematics, University of Exeter, Exeter.
BSRBR-RA Contributors Group

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo identify different trajectories of disease activity in patients with RA following initiation of a first anti-TNF.

methodsPatients with RA starting their first anti-TNF between 2001 and 2013 were selected from the British Society for Rheumatology Biologics Register for RA. Six-monthly DAS28-ESR scores were used to identify trajectories of disease activity using latent class modelling. Data were included for six follow-ups after registration (approximately 3 years). Subgroup analysis examined changes in disease activity profiles over time.

resultsA total of 14 436 patients with RA starting their first anti-TNF were enrolled between 2001 and 2013 (13 115 between 2001 and 2008, 1321 between 2010 and 2013). The mean number of DAS28-ESR scores was 3.5/patient (s.d. 2.1), with a mean of 184.9 days (s.d. 69.9) between scores. The DAS28-ESR nadir was achieved within 250 days of commencing anti-TNF, although apparent trajectory divergence emerged by first 6-monthly follow-up at 180 days. Four distinct response trajectories comprised the most stable model. Most patients fitted into 'modest' (7986 patients; 55.3%) or 'substantial' (4676 patients; 32.4%) response trajectories. Of the remainder, 1254 (8.7%) and 520 (3.6%) fitted 'maximal' and 'minimal' response trajectories, respectively. There was a significant (P < 0.01) increase in proportion achieving 'maximal' response between 2001-2008 and 2010-2013.

conclusionThis is the largest study to identify long-term response trajectories with anti-TNF. By 6 months, longer-term trajectory profiles of DAS28 could already be identified, with many patients identified earlier. The majority of patients had persistent moderate response, equivalent to maintained DAS28-ESR moderate disease activity. The maximal response trajectory (equivalent to sustained DAS2-ESR remission) was only achieved by approximately one-third of patients.

Indexed as

AdultAgedAntirheumatic AgentsArthritis, RheumatoidDisease ProgressionFemaleHumansMaleMiddle AgedPrognosisRegistriesRemission InductionSeverity of Illness IndexTreatment OutcomeTumor Necrosis Factor InhibitorsAntirheumatic AgentsTumor Necrosis Factor Inhibitorsbiologic therapiesDMARDSepidemiologyoutcome measuresrheumatoid arthritis

Identifiers

PMID31714580
PMCPMC7310091

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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.