Evidence map›Paper›PMID 41499038›Full record

ArticleRheumatology and therapy2026

Quantifying Disease Activity Despite Treatment with Tumor Necrosis Factor Inhibitors Among Patients with Psoriatic Arthritis and Axial Spondyloarthritis: Real-World Results from the PPD CorEvitas Psoriatic Arthritis/Spondyloarthritis Registry.

Philip Mease, Xiaolan Ye, Christopher D Saffore, Bhumik Parikh, Sandra Ciecinski, Taylor Blachley, Melissa Eliot, Nicole Middaugh, Alexis Ogdie

Abstract read
In one paragraph

Article in Rheumatology and therapy, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

9 authors.

Philip MeaseProvidence Swedish Medical Center and University of Washington, Seattle, WA, USA.ORCID http://orcid.org/0000-0002-6620-0457
Xiaolan YeAbbVie Inc., 1 N Waukegan Road, Dept. GMH1, ABV1 4NW-102-04, North Chicago, IL, 60064-6078, USA.
Christopher D SafforeAbbVie Inc., 1 N Waukegan Road, Dept. GMH1, ABV1 4NW-102-04, North Chicago, IL, 60064-6078, USA. christopher.saffore@abbvie.com.ORCID http://orcid.org/0000-0003-0396-2646
Bhumik ParikhAbbVie Inc., 1 N Waukegan Road, Dept. GMH1, ABV1 4NW-102-04, North Chicago, IL, 60064-6078, USA.
Sandra CiecinskiAbbVie Inc., 1 N Waukegan Road, Dept. GMH1, ABV1 4NW-102-04, North Chicago, IL, 60064-6078, USA.
Taylor BlachleyThermo Fisher Scientific, Waltham, MA, USA.
Melissa EliotThermo Fisher Scientific, Waltham, MA, USA.
Nicole MiddaughThermo Fisher Scientific, Waltham, MA, USA.
Alexis OgdieDepartments of Medicine and Epidemiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionAlthough tumor necrosis factor inhibitors (TNFis) have improved management of psoriatic arthritis (PsA) and axial spondyloarthritis (axSpA); many patients experience suboptimal disease control. We quantified achievement of varying degrees of disease activity in patients with PsA and axSpA who initiated and maintained TNFi treatment for 12 months.

methodsPatients with PsA or axSpA enrolled in the PPD™ CorEvitas™ PsA/Spondyloarthritis Registry were included in the study. Varying degrees of disease control were quantified based on minimal disease activity (MDA) status for PsA and BASDAI50 (≥ 50% improvement in Bath Ankylosing Spondylitis Disease Activity Index) status for axSpA at 6 and 12 months. Patients were categorized into four groups: sustained (MDA/BASDAI50 at 6 and 12 months), improved (MDA/BASDAI50 at 12 months only), worsened (MDA/BASDAI50 at 6 months only), and never achieved (no MDA/BASDAI50 at 6 or 12 months).

resultsFor PsA, 338 patients initiated and persisted on TNFis. At 6 months, the majority (65%, n = 221) did not achieve MDA status; of these, 86% (n = 189) still did not achieve MDA at 12 months. For axSpA, 152 patients initiated and persisted on TNFis. At 6 months, 80% (n = 121) did not achieve BASDAI50; among these patients, 91% (n = 110) still did not achieve BASDAI50 status at 12 months. For both PsA and axSpA initiators, the risk of not achieving clinical or quality of life outcomes was two- to threefold lower in patients who never achieved versus patients who achieved and sustained MDA/BASDAI50.

conclusionMore than 80% of patients with PsA or axSpA who did not achieve low disease activity at 6 months still did not achieve low disease activity by 12 months even though they persisted on TNFi treatment. These findings underscore the importance for physicians to consider modifying therapy if treatment targets with TNFi have not been achieved in the first 6 months.

Indexed as

Axial spondyloarthritisBack painCorEvitas PsA/SpA RegistryImmune-mediated inflammatory diseaseJoint painMinimal disease activityPhysical functionPsoriatic arthritisQuality of lifeTumor necrosis factor inhibitors

Identifiers

PMID41499038
PMCPMC12996473

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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.