Evidence map›Paper›PMID 38308727›Full record

ArticleRheumatology and therapy2024

Etanercept in Axial Spondyloarthritis, Psoriatic Arthritis, and Plaque Psoriasis: Real-World Outcome Data from German Non-interventional Study ADEQUATE.

Eugen Feist, Xenofon Baraliakos, Frank Behrens, Diamant Thaçi, Anja Plenske, Pascal Klaus, Thomas Meng

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Rheumatology and therapy, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02486302 (A PROSPECTIVE, MULTICENTER NON-INTERVENTIONAL STUDY TO EVALUATE THE EFFICACY OF ENBREL), which is not on this map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.5field-weighted citation impact, top 39% 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.

NCT02486302 completednot on this map

A prospective, multicenter non-interventional study to evaluate the efficacy of enbrel (registered) (etanercept) over a period of 12 months in the routine treatment of patients with rheumatoid arthritis, axial spondyloarthritis, psoriatic arthritis, or plaque psoriasis with particular focus on the clinical status improvements still observable after 12 weeks of treatment

TypeobservationalSponsorPfizerRan2015 to 2017Enrolled1,534ConditionsRheumatoid Arthritis, Psoriatic Arthritis, Axial Spondyloarthritis, Plaque PsoriasisArmsEtanercept
3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. 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

7 authors at 5 institutions in 1 country.

Eugen FeistDepartment of Rheumatology, Helios Fachklinik, Sophie-von-Boetticher-Straße 1, 39245, Vogelsang-Gommern, Germany. eugen.feist@helios-gesundheit.de.ORCID http://orcid.org/0000-0002-9872-5282
Xenofon BaraliakosRheumazentrum Ruhrgebiet Herne, Ruhr-University, Bochum, Germany.ORCID http://orcid.org/0000-0002-9475-9362
Frank BehrensCIRI/Rheumatology and Fraunhofer IME, Institutsteil Translationale Medizin and Pharmakologie, Klinikum Goethe-Universität, Frankfurt am Main, Germany.ORCID http://orcid.org/0000-0001-8750-7186
Diamant ThaçiInstitute and Comprehensive Center Inflammation Medicine, University of Lübeck, Lübeck, Germany.ORCID http://orcid.org/0000-0001-8513-550X
Anja PlenskePfizer Pharma GmbH, Berlin, Germany.
Pascal KlausPfizer Pharma GmbH, Berlin, Germany.
Thomas MengPfizer Pharma GmbH, Berlin, Germany.
Pfizer (Germany) · DEGoethe University Frankfurt · DEHelios Kliniken · DERheumazentrum Ruhrgebiet · DEUniversity of Lübeck · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionFor chronic diseases such as axial spondyloarthritis (axSpA), psoriatic arthritis (PsA), and plaque psoriasis (PsO), treatment goals include remission or at least low disease activity (LDA) by 12 weeks. Improvements in symptoms such as pain and fatigue should also be treatment goals.

methodsADEQUATE was a German, prospective, non-interventional study to evaluate the proportion of patients with rheumatoid arthritis, PsA, axSpA, or PsO who, in routine clinical practice, benefit from the continuation of treatment with etanercept (ETN) beyond 12 weeks, even when their treatment goals have not yet been reached. Patient-reported outcomes (PROs) and changes in concomitant glucocorticoid use were also recorded. This article focuses on results for patients with axSpA and PsA; data for patients with PsO are described briefly.

resultsIn total, 305, 254, and 70 patients with axSpA, PsA, and PsO, respectively, were included. Rates of remission at week 12 and week 24, respectively, were 19% and 18% for axSpA, 38% and 51% for PsA, and 7% and 19% for PsO. Rates of LDA at week 12 and week 24, respectively, were 39% and 45% for axSpA, 50% and 60% for PsA, and 34% and 51% for PsO. Extending treatment up to 52 weeks was associated with stable rates of or further increases in remission and LDA rates. Improvements in pain, fatigue, and depression (axSpA, PsA, and PsO) and reductions in concomitant glucocorticoid use (axSpA and PsA) were observed. No new safety signals were detected.

conclusionThese findings confirm the effectiveness and safety of ETN in routine clinical practice for several indications and highlight potential benefits of continuing ETN treatment in patients who have not reached their treatment goals after 12 weeks. Additional benefits included improvements in PROs and reduction of concomitant glucocorticoids.

trial registrationClinicalTrials.gov NCT02486302.

Indexed as

Axial spondyloarthritisEtanerceptPlaque psoriasisPsoriatic arthritisReal worldRemission

Identifiers

PMID38308727
PMCPMC10920535
OpenAlexW4391515148

What OpenQuestion holds

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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.